Professional Documents
Culture Documents
Verlag fr Naturheilkunde
Disclaimer:
The purpose of this book is to provide information about the use of the SANUM
preparations for a wide range of medical problems only. However, illness can
be highly unpredictable, and therefore, one should seek the best possible
medical expertise. No liability is accepted by the author and/or the publishers
for any claims arising from the administration, prescribing strategy or use of
any of the remedies described.
To the Reader:
This Isopathic/Homeopathic Materia Medica of Sanum medicinal products has
been compiled from research conducted by leading homeopathic practitioners
in and outside of Germany. The collected research and uses discussed in the
Materia Medica have been reviewed by a distinguished panel. This valuable
compilation of known medicinal uses of the Isopathic/Homeopathic remedies is
made available to interested practitioners and researchers in many countries.
The production process of the homeopathics covered by this Materia Medica is
strictly based on the German Homeopathic Pharmacopoeia (Homopathisches
Arzneimittelbuch), which essentially has been adopted by many other countries.
However, because not all products, dosage forms or intended uses are available
or approved by the relevant authorities in all national markets, practitioners
are advised to seek local guidance regarding the legal status of the products,
intended uses and type of application in their areas. For example, the oral por-
table SIPS (1 and 2 ml vials) are at this time available only in the United States
of America.
Our thanks to all those who have made publication of this Materia Medica possible
and to the peer reviewers and practitioners who have contributed their time
and effort to disseminate this information.
Dr. Konrad Werthmann
Isopathic/Homeopathic
Materia Medica
Edition 2012
Published by Semmelweis-Institut
Verlag fr Naturheilkunde GmbH
D - 27316 Hoya. Copyright by Semmelwels-Institut
All rights reserved, including those of translations into foreign languages. It is not permitted to
reproduce any part of this book in any form, copying, printing, microlming or scanning or audio
taping without written permission of the publisher.
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cualquier forma que sea, electrnica o mecnica; mediante fotocopia, mimegrafo o
cualquier sistema de grabacin en disco o cinta de ordenador.
Edition 2012
Printed in Germany by Druckerei Adam Prettenhofer GmbH & Co. KG
5
Contents
Preface 9
SANUM Excretion Cure 21
4-Steps-Basic Scheme of SANUM Therapy according to Dr. Werthman 22
Albicansan
Spermus)
Leptucin
Leptu)
Lipiscor
(fungal preparation) Drops 5X, Amps. 5X, 6X, 7X; Tabs. 5X, 96
Caps. 4X, Supps. 3X, Ointment 3X, Eye Drops 5X
Mucokehl
(fungal preparation) Drops 5X, Amps. 5X, 6X, 7X; Tabs. 5X, 128
Caps. 4X, Supps. 3X, Ointment 3X
Nota-Quent
(fungal preparation) Drops 5X 143
Okoubasan
(fungal preparation) Drops 5X, Amps. 5X, Caps. 4X, Supps. 4X 156
Pleo Chelate
Drops 160
Polysan A (in vitro diagnosticum) Drops 9X 162
Polysan D (in vitro diagnosticum) Drops 9X 164
Polysan Dx (in vitro diagnosticum) Drops 9X 166
7
Polysan E (in vitro diagnosticum) Drops 9X 168
Polysan G (in vitro diagnosticum) Drops 9X 170
Polysan K (in vitro diagnosticum) Drops 9X 172
Polysan M (in vitro diagnosticum) Drops 9X 174
Polysan Om (in vitro diagnosticum) Drops 9X 176
Polysan R (in vitro diagnosticum) Drops 9X 178
Polysan T (in vitro diagnosticum) Drops 9X 180
Quentakehl
(fungal preparation) Drops 5X, Amps. 5X, Caps. 4X, Supps. 3X 182
Rebas
(organ preparation) Amps. 5X, 12X; Caps. 4X, 6X; Supps. 4X, 6X 190
Recarcin
(bacterial preparation) Drops 6X, Amps. 4X, 6X; Caps. 4X, 6X; Supps. 6X 196
Relivora
, Candida albicans
EXMYKEHL
, Peniclllium roquefortii
MUCEDOKEHL
, Mucor mucedo
MUCOKEHL
, Mucor racemosus
NIGERSAN
, Aspergillus niger
NOTAKEHL
, Penicillium chrysogenum
PEFRAKEHL
, Candida parapsilosis
QUENTAKEHL
, Penicillium glabrum
RUBERKEHL
, Aspergillus ruber
SANKOMBI
, FOMEPIKEHL
, LARIFIKEHL
, MUSCARSAN
,
PINIKEHL
, RUBERKEHL
represent fungal preparations, which have had traditional healing reputations in
folk medicine; these preparations are produced as isopathic substances based
on the knowledge of Prof. Dr. Enderlein.
Treatment of Candidiasis with Isopathic Preparations
ALBICANSAN
.
Moreover, the well-proven preparation PEFRAKEHL
is a pre-
paration from the yeast form of Candida parapsilosis, which is predominantly
isolated from the skin, from nail bed infections, otitis externa and endocarditis
in human beings.
14
EXMYKEHL
Atox 6X (Anti-Chondritins),
the elimination of each form of decomposition is accelerated.
As a rule, it is important to ensure the function of the organs of elimination (stool,
urine, sweat, sputum). Possibly, a detoxication therapy (enemas, baths, teas,
electrolytes) may be required.
Because MUCOKEHL
, SANUVIS
, CITROKEHL
and
FORMASAN are suitable for this purpose.
In regard to additional biological therapy in general, the therapist naturally re-
mains in control of all possibilities during the period of isopathic treatment.
Unfortunately, the fact that focal disturbance elds can limit or cancel the ef-
fectiveness of every holistic treatment is often to be taken into account suf-
ciently. It should be a precondition to examine the patient and to undertake
sanitizations before the administration of isopathic/homeopathic preparations.
Not only should the usual foci in teeth, tonsils, paranasal sinuses, intestine, etc.
be considered, but also the amalgam llings that play an important part in the
sense of focal toxicoses through years of releasing mercury. The replacement of
these llings by neutral materials is desirable.
In all diseases from the Endobiosis complex a nutrition rich in vitamins and vital
substances is of fundamental importance. It is a precondition, not only for the
15
healing process, but also for the effectiveness of every isopathic and immuno-
biological treatment of endobiontic conditions. Nutritional intake requires spe-
cial attention in cases of Endobiosis, including cancer. It should be vegetarian,
rich in raw foods, free from superne our, sugar, and all addictive substances.
With a vegetarian diet, attention must be given to include sufcient lactic acid
food for the body.
The Immunobiological Preparations from the Bacterial Phase
Beside the previously described isopathic preparations of the fungal phase, the
immunobiological preparations from the bacterial phase ll an important place
in biological therapy:
ARTHROKEHLAN
, Mycobacterium bovis
LATENSIN
, Propionibacterium avidum
RECARCIN
).
2. Bacillus Species
In folk medicine, tea decoctions using hay, excrement from cows, or peat moss
have long been used, without any knowledge of their containing Bacillus subtilis
as active agent. Farmers in many countries utilized hay infusions for curing in-
testinal diseases in cattle.
As early as 1887, Metchnikoff described the growth-inhibiting effect of aerobic
soil bacteria, particularly of Bacillus subtilis, against pathogens such as Strep-
tococci, Staphylococci, Salmonella and Mycobacterium tuberculosis.
Works by Ramon and Richou, as well as Jansen and Hirschmann in 1943/44
showed the antitoxic and antibiotic properties of the pathogen, which was gen-
erally referred to as Hay bacillus.
However, the rst reports about the oral, subcutaneous and intravenous appli-
cation of Bacillus subtilis strains came from the former SANUM company in the
years 1938/39 with outstanding therapeutic results. Particularly, its effective-
ness with certain pseudotubercular forms was discovered at that time. The
general stimulating effect on the nonspecic defensive capacity of the human
organism already showed up in these beginnings of Subtilis Therapy. The name
UTILIN
has been used under trade mark protection for this new, special re-
medy since 1939. In later years, additional Bacillus strains that are closely re-
lated to Bacillus subtilis found their entry into the therapy under the product
names of LATENSIN
and RECARCIN
.
Preparations with Bacillus species have manifold immunostimulating effects. Clini-
cal observations yielded good success in recurring diseases of the urinary tract
and the respiratory organs, in patients with defective immune situations, in
food allergies, as well as other chronic diseases that were brought about by a
reduced immune status (J. Hartmann, Therapeutikon 4, 1990).
3. Corynebacteria and Propionibacteria
The immunobiological preparations ARTHROKEHLAN
"U" 6X.
An additional therapeutic development with Corynebacteria followed in the ap-
plication of Corynebacterium parvum for infection prophylaxis. This strain was
later reclassied as Propionibacterium acnes. The activation of the monocyte-
macrophage system is a general characteristic of the species Propionibacterium.
Its antibacterial, antiviral, antiparasitic and antitumoral actions are the result.
The latter, in particular, have been intensively examined in the strain Propionibac-
terium avidum. Its stimulatory effects on the hematopoietic system qualify it in
immune therapy especially for treatment of myelosuppressive side effects of a
cytostatic or radiation therapy.
4. Sanukehl Preparations - Polysaccarides for Haptenic Therapy
Bacteria and fungi produce toxins which can be the causal trigger for the deve-
lopment of specic diseases. In addition, microbes can develop as microorganis-
ms called Cell Wall Decient (CWD) forms. Toxins and cell wall decient forms,
however, cannot be recognized by the bodys immune system due to missing
antigen properties. In the mode of action, SANUKEHL
"N" is the
perfect treatment, also in cases of excessive acidication of the gastrointestinal
tract with its consequences, such as heartburn and gas.
CITROKEHL
lies in the various potencies which are brought together within the preparation.
The lower potencies serve the raising of cellular respiration, while the higher
potencies serve the elimination of excessive lactic acid concentrations, especially
of the nonphysiological D-(-) lactic acid.
Organ Preparations
THYMOKEHL activates metabolism, stimulates the pre-stages of the T-
lymphocytes to maturation and strengthens the immune system.
CHRYSOCOR
, OKOUBASAN
, and USNEABASAN
, made
from the lichen Usnea barbata, is predominantly used for illnesses in the head
area (headaches, sunstroke) and together with LUFFASAN
is indicated for the stimulation of the liver and kidney function and
thus achieving a cleansing of the connective tissue and blood as well.
Mineral and Trace Element Preparations
An important factor for the maintenance of our health lies in providing the body
with necessary mineral and trace elements. Regulatory processes in the organ-
ism, which are the precondition for a regulated metabolic process, cannot take
their course without a stable electrolyte equilibrium of ions, such as sodium, po-
tassium, calcium and magnesium.
The trace elements, which according to their name are needed by the body in
only very small amounts, enter catalytically into the metabolic processes. With-
out the presence of these Bio-catalysts - including iron, zinc, manganese,
copper, cobalt, iodine and uorine - many processes that are essential for life
cannot take their course, such as the action of the heart.
These mineral and trace element preparations are offered for a broad applica-
tion spectrum: ALKALA
L (Mg), SELENOKEHL
(Se),
ZINKOKEHL
Preparations:
Not suitable for children under 2 years. Children over 2 years: as topical ad-
ministration 1x 1 drop for every year of age (e.g. 5 drops for a 5 year old child)
every 1 or 2 days; Children over 8 years: dosage as for adults.
Bacterial Preparations:
Not suitable for children under 2 years. Children over 2 years: as topical ad-
ministration 1x 1 drop for every year of age (e.g. 5 drops for a 5 year old child)
once or twice weekly; Children over 8 years: dosage as for adults.
22
4-Steps-Basic Scheme of SANUM Therapy according to
Dr. Werthmann
Duration of the treatment: 6 to 8 weeks (depending on the clinical picture and
the course of treatment)
Step 1: Milieu Regulation during the complete therapy duration
Change of nutrition to repair the intestinal mucosas atrophy by omitting
the primary antigens (cows milk and hens eggs)
Deacidication / detoxication:
ALKALA
N, SANUVIS
, CITROKEHL
, FORMASAN;
CERIVIKEHL
, OKOUBASAN
, USNEABASAN
Substitution:
SELENOKEHL
, ZINKOKEHL
, MAPURIT
L, LIPISCOR
, Vitamins
At the same time start with
Step 2: Specic Regulation with fungal preparations
NOTAKEHL
(bacterial affections) or
QUENTAKEHL
(viral affections) or
FORTAKEHL
(intestine affections) or
EXMYKEHL
(fungal affections) or
PEFRAKEHL
(fungal affections) or
GRIFOKEHL (herpes affections) or
ALBICANSAN
(candida affections) or
LARIFIKEHL
in the evening or
2x daily SANKOMBI
for 5 days,
alternatively with the fungal preparation used in Step 2 for 2 days.
(From Monday to Friday: MUCOKEHL
/NIGERSAN
or SANKOMBI
, RECARCIN
, UTILIN
or UTILIN
S, BOVISAN
;
SANUKEHL
preparations
23
Albicansan
3X
Ointment
for rubbing in
Active ingredient: Candida albicans e volumine cellulae (lyophil., steril.) 3X
Composition: 1 g ointment contains: Medically active substance: 0.1 g Candida
albicans e volumine cellulae (lyophil., steril.) 3X dil. Other
constituents: 0.38 g lanolin alcohol ointment, 0.10 g coconut oil fract.,
0.03 g glyceryl monostearate 40-55%, 0.23 g propylene glycol, 0.02
g magnesium sulphate x 7 H2O, 0.01 g lactic acid, 0.13 g water for
injection.
According to experience, Mycoses and secondary mycotic, infectious skin disorders, balanitis,
to be administered in vulvitis, pruritis genitalis.
cases of:
Characteristics: Albicansan
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Candida albicans).
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: Candida albicans as an active ingredient is also contained in Exmykehl
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X, 30 g tube
of ointment 3X.
24
Albicansan
3X
Suppositories
for rectal application
Active ingredient: Candida albicans e volumine cellulae (lyophil., steril.) 3X
Composition: 1 suppository contains: Medically active substance: 0.2 g Candida
albicans e volumine cellulae (lyophil., steril.) 3X trit. Other
constituents: hard fat, lactose.
According to experience, Mycoses and secondary mycotic, infectious skin disorders, diseases
to be administered in of the mouth, like stomatitis, gingivitis, perlche, aphthae, mycoses
cases of: of the urogenital tract, such as vaginitis, urethritis, possibly for adnexitis,
mycoses of the gastrointestinal tract.
Characteristics: Albicansan
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Candida albicans).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Albicansan
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
Candida albicans as an active ingredient is also contained in Exmykehl
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X, 30 g tube
of ointment 3X.
25
Albicansan
4X
Capsules
for oral intake
Active ingredient: Candida albicans e volumine cellulae (lyophil., steril.) 4X
Composition: 1 capsule contains: Medically active substance: 330 mg Candida
albicans e volumine cellulae (lyophil., steril.) 4X trit. Other
constituents: lactose, hypromellosis (capsule shell).
According to experience, Mycoses and secondary mycotic, infectious skin disorders, diseases
to be administered in of the mouth, like stomatitis, gingivitis, perlche, aphthae, mycoses of
cases of: the urogenital tract, such as vaginitis, urethritis, possibly for adnexitis,
mycoses of the gastrointestinal tract.
Characteristics: Albicansan
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Candida albicans).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Albicansan
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
Candida albicans as an active ingredient is also contained in
Exmykehl
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X, 30 g tube
of ointment 3X.
26
Albicansan
5X
Ampules
Liquid dilution for injection
Active ingredient: Candida albicans e volumine cellulae (lyophil., steril.) 5X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Candida
albicans e volumine cellulae (lyophil., steril.) 5X aquous dil.
Other constituents: isotonic sodium chloride solution.
According to experience, Mycoses and secondary mycotic, infectious skin disorders, diseases of
to be administered in the mouth, like stomatitis, gingivitis, perlche, aphthae, mycoses of
cases of: the urogenital tract, such as vaginitis, urethritis, possibly for adnexitis,
mycoses of the gastrointestinal tract.
Characteristics: Albicansan
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Candida albicans).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Albicansan
.
with other remedies: An interval of 4 weeks before and After treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: Candida albicans as an active ingredient is also contained in
Exmykehl
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X, 30 g tube
of ointment 3X.
27
Albicansan
5X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Candida albicans e volumine cellulae (lyophil., steril.) 5X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml
Candida albicans e volumine cellulae (lyophil., steril.) 5X dil.
Other constituents: puried water.
According to experience, Mycoses and secondary mycotic, infectious skin disorders, diseases of
to be administered in the mouth, like stomatitis, gingivitis, perlche, aphthae, mycoses of
cases of: the urogenital tract, such as vaginitis, urethritis, possibly for adnexitis,
mycoses of the gastrointestinal tract.
Characteristics: Albicansan
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Candida albicans).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Albicansan
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: After opening, contents must be used within two months. Candida
albicans as an active ingredient is also contained in Exmykehl
.
Duration of treatment: Dependent on the advice of the physician or health careprofessional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X, 30 g tube
of ointment 3X.
28
Alkala
N
Powder
Active ingredients: sodium hydrogen carbonate, potassium hydrogen carbonate,
sodium citrate
Composition: 150 g powder contain: 2.67 g sodium hydrogen carbonate x
H2O, 13.40 g potassium hydrogen carbonate, 133.93 g sodium
citrate.
Indications: Alkalisation, acidosis of the stomach and the duodenum, heartburn,
gastritis and ulcus ventriculi, liver and gallbladder troubles, repletion
and atulence, rheumatic diseases, chronic skin diseases and diseases
of the respiratory and urogenital tract.
Characteristics: Alkala
N
Powder
This composition of Alkala
A 6X
Ampules
Liquid dilution for injection
Active ingredient: Propionibacterium acnes culturae ltratum (lyophil., steril.)
6X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Propioni-
bacterium acnes culturae ltratum (lyophil., steril.) 6X aquous
dil. Other constituents: isotonic sodium chloride solution.
According to experience, Arthritic, arthrotic, as well as degenerative diseases of the spinal column,
to be administered in myalgia.
cases of:
Characteristics: Arthrokehlan
A,
theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.
Contraindications: Fever, conditions of weakness.
Do not administer in cases of known hypersensitivity to Propioni-
bacterium acnes.
Adverse reactions: None known. Generally well tolerated. Occasionally local reactions
like rubefaction, swelling or painfulness may be observed, normally
vanishing without treatment. These effects are not to be seen as
adverse reactions, but rather as an expression of effectiveness. In the
rst 2 or 3 days after the injection sometimes conditions of weakness,
fortied expectoration, slight painfulness of the region or subfebrile
temperatures may show. Strong general reactions are always a sign of
overdose or of incorrect injection technique.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: None.
33
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.
34
Arthrokehlan
A 6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Propionibacterium acnes culturae ltratum (lyophil., steril.)
6X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml
Propionibacterium acnes culturae ltratum (lyophil., steril.)
6X dil. Other constituents: puried water.
According to experience, Arthritic, arthrotic, as well as degenerative diseases of the spinal column,
to be administered in myalgia.
cases of:
Characteristics: Arthrokehlan
A,
theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.
Contraindications: Fever, conditions of weakness.
Do not administer in cases of known hypersensitivity to Propioni-
bacterium acnes.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.
35
Arthrokehlan
U 6X
Ampules
Liquid dilution for injection
Active ingredient: Corynebacterium stationis culturae ltratum (lyophil., steril.)
6X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Coryne-
bacterium stationis culturae ltratum (lyophil., steril.) 6X
aquous dil. Other constituents: isotonic sodium chloride solution.
According to experience, Stimulation of endogenic defense capacities, adjuvant in anti-carcino-
to be administered in genic therapy.
cases of:
Characteristics: Arthrokehlan
U,
theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.
Contraindications: Fever, conditions of weakness.
Do not administer in cases of known hypersensitivity to Coryne-
bacterium stationis.
Adverse reactions: None known. Generally well tolerated. Occasionally local reactions
like rubefaction, swelling or painfulness may be observed, normally
vanishing without treatment. These effects are not to be seen as
adverse reactions, but rather as an expression of effectiveness. In the
rst 2 or 3 days after the injection sometimes conditions of weakness,
fortied expectoration, slight painfulness of the region or subfebrile
temperatures may show. Strong general reactions are always a sign of
overdose or of incorrect injection technique.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
36
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.
37
Arthrokehlan
U6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Corynebacterium stationis culturae ltratum (lyophil., steril.)
6X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Coryne-
bacterium stationis culturae ltratum (lyophil., steril.) 6X dil.
Other constituents: puried water.
According to experience, Stimulation of endogenic defense capacities, adjuvant in anti-carcino-
to be administered in genic therapy.
cases of:
Characteristics: Arthrokehlan
U,
theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.
Contraindications: Fever, conditions of weakness.
Do not administer in cases of known hypersensitivity to Coryne-
bacterium stationis.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.
38
Bovisan
5X
Capsules
for oral intake
Active ingredient: Mycobacterium bovis (BCG) e volumine ex muris cellulae
(lyophil., steril.) 5X
Composition: 1 capsule contains: Medically active substance: 330 mg Myco-
bacterium bovis (BCG) e volumine ex muris cellulae (lyophil.,
steril.) 5X trit. Other constituents: lactose, hypromellosis (capsule shell).
According to experience, Chronic inammation, rheumatic disorders, diseases connected to tuber-
to be administered in culinic constitution; immune modulation.
cases of:
Characteristics: This product is obtained by a special preparation and culture technique
of a stock solution of Mycobacterium bovis which ensures both non-
pathogenic and immunomodulating properties.
Application: Unless otherwise prescribed: 1-2 x weekly 1 capsule.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Bovisan
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
Do not administer in cases of known hypersensitivity to Mycobacterium
bovis.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions Immunosuppressive drugs can inuence the effectivity of Bovisan
. An
with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X, 5 capsules 5X, 10 suppositories 5X.
39
Bovisan
5X
Suppositories
for rectal application
Active ingredient: Mycobacterium bovis (BCG) e volumine ex muris cellulae
(lyophil., steril.) 5X
Composition: 1 suppository contains: Medically active substance: 0.2 g Myco-
bacterium bovis (BCG) e volumine ex muris cellulae (lyophil.,
steril.) 5X trit. Other constituents: hard fat, lactose.
According to experience, Chronic inammation, rheumatic disorders, diseases connected to tuber-
to be administered in culinic constitution; immune modulation.
cases of:
Characteristics: This product is obtained by a special preparation and culture technique
of a stock solution of Mycobacterium bovis which ensures both non-
pathogenic and immunomodulating properties.
Application: Unless otherwise prescribed: 1-3 x weekly insert 1 suppository rectally.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Bovisan
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
Do not administer in cases of known hypersensitivity to Mycobacterium
bovis.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions Immunosuppressive drugs can inuence the effectivity of Bovisan
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X, 5 capsules 5X, 10 suppositories 5X.
40
Bovisan
6X
Ampules
Liquid dilution for injection
Active ingredient: Mycobacterium bovis (BCG) e volumine cellulae (lyophil., steril.)
6X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Myco-
bacterium bovis (BCG) e volumine cellulae (lyophil., steril.)
6X aquous dil. Other constituents: isotonic sodium chloride solution.
According to experience, Chronic inammation, rheumatic disorders, diseases connected to tuber-
to be administered in culinic constitution; immune modulation.
cases of:
Characteristics: This product is obtained by a special preparation and culture technique
of a stock solution of Mycobacterium bovis which ensures both non-
pathogenic and immunomodulating properties.
Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either
intramuscularly or subcutaneously 1-2 x weekly.
Side effects: Because of specic organic components of Bovisan
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
Do not administer in cases of known hypersensitivity to Mycobacterium
bovis.
Adverse reactions: None known. Generally well tolerated. Occasionally local reactions
like rubefaction, swelling or painfulness may be observed, normally
vanishing without treatment. These effects are not to be seen as
adverse reactions, but rather as an expression of effectiveness. In the
rst 2 or 3 days after the injection, sometimes conditions of weakness,
fortied expectoration, slight painfulness of the region or subfebrile
temperatures may occur. Strong general reactions are always a sign of
overdosage or of incorrect injection technique. In this case the treatment
can be continued orally with Bovisan
drops or capsules.
Interactions Immunosuppressive drugs can inuence the effectivity of Bovisan
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: None.
41
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X, 5 capsules 5X, 10 suppositories 5X.
42
Bovisan
6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Mycobacterium bovis (BCG) e volumine cellulae (lyophil., steril.)
6X
Composition: 5 ml liquid dilution contain: Medically active substance: 5 ml Myco-
bacterium bovis (BCG) e volumine cellulae (lyophil., steril.)
6X dil. Other constituents: puried water.
According to experience, Chronic inammation, rheumatic disorders, diseases connected to
to be administered in tuberculinic constitution; immune modulation.
cases of:
Characteristics: This product is obtained by a special preparation and culture technique
of a stock solution of Mycobacterium bovis which ensures both non-
pathogenic and immunomodulating properties.
Application: Unless otherwise prescribed: For oral intake: 1-3 x weekly 2-5 drops.
For rubbing in: 1-3 x weekly 2-5 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Bovisan
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
Do not administer in cases of known hypersensitivity to Mycobacterium
bovis.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions Immunosuppressive drugs can inuence the effectivity of Bovisan
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X, 5 capsules 5X, 10 suppositories 5X.
43
Calvakehl
3X
Drops
Liquid dilution for oral intake
Active ingredient: Calvatia gigantea e sporibus 3X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml
Calvatia gigantea e sporibus 3X dil. Other constituents: puried
water, ethanol 62 % (m/m).
According to experience, Bleeding tendency, such as nose bleeding or uterus bleeding; weakness
to be administered in of the heart and circulatory system with blood congestion; lack of oxygen in
cases of: blood; skin rashes; indigestion and diarrhea.
Characteristics: Calvakehl
is produced from the Giant bovista fungus. In the 16th
century, the application was already well known in folk medicine for its
hemostyptic and wound healing properties.
Application: Unless otherwise prescribed:
For oral intake: 1-3 x daily 5-10 drops.
Side effects: Because of specic organic components of Calvakehl
,
theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Calvatia
gigantea.
This product contains 70 % (v/v) alcohol (ethanol). Following the
dosage recommendations, 10 drops lead to an alcohol intake of 0.11
g. This may present a health risk in cases of liver diseases, alcoholism,
epilepsy, brain damage, pregnancy, and in children. The action of other
drugs may be reduced or intensied.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains 70 % (v/v) alcohol (ethanol).
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml and 30 ml dropper
bottle 3X, 80 tablets 4X.
44
Calvakehl
4X
Tablets
for oral intake
Active ingredient: Calvatia gigantea e sporibus 4X
Composition: 1 tablet contains: Medically active substance: 250 mg Calvatia
gigantea e sporibus 4X trit. Other constituents: lactose, potato
starch, magnesium stearate.
According to experience, Bleeding tendency, such as nose bleeding or uterus bleeding; weakness
to be administered in of the heart and circulatory system with blood congestion; lack of oxygen
cases of: in blood; skin rashes; indigestion and diarrhea.
Characteristics: Calvakehl
is produced from the Giant bovista fungus. In the 16th
century, the application was already well known in folk medicine for its
hemostyptic and wound healing properties.
Application: Unless otherwise prescribed:
For oral intake: 1-3 x daily 1 tablet.
Side effects: Because of specic organic components of Calvakehl
,
theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Calvatia
gigantea.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml and 30 ml dropper
bottle 3X, 80 tablets 4X.
45
Cerivikehl
1X
Drops
Liquid dilution for oral intake
Active ingredient: Cetraria islandica mother tincture
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Cetraria
islandica 1X dil. Other constituents: puried water, ethanol 62% (m/m).
According to experience, Diseases of the respiratory system, sinusitis, laryngitis, bronchitis, dry
to be administered in cough; lack of appetite.
cases of:
Characteristics: Cerivikehl
,
theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: This product contains 70 % (v/v) alcohol (ethanol). Following the
dosage recommendations, 10 drops lead to an alcohol intake of 0.11
g. This may present a health risk in cases of liver diseases, alcoholism,
epilepsy, brain damage, pregnancy, and in children. The action of other
drugs may be reduced or intensied.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains 70 % (v/v) alcohol (ethanol).
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 30 ml dropper bottle 1X, 2 ml
ampule 10 and 50 3X.
46
Cerivikehl
3X
Ampules
Liquid dilution for injection
Active ingredient: Cetraria islandica 3X
Composition: 1 ampule of 2 ml contains: Medically active substance: 2 ml
Cetraria islandica 3X aquous dil. Other constituents: isotonic
sodium chloride solution.
According to experience, Diseases of the respiratory system, sinusitis, laryngitis, bronchitis, dry
to be administered in cough; lack of appetite.
cases of:
Characteristics: Cerivikehl
,
theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: None known.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 30 ml dropper bottle 1X, 2 ml
ampule 10 and 50 3X.
47
Chrysocor
5X
Ampules
Liquid dilution for injection
Active ingredient: Placenta hydrolysate (lyophil., steril.) 5X
Composition: 1 ampule of 2 ml contains: Medically active substance: 2 ml Placenta
hydrolysate (lyophil., steril.) 5X aquous dil. Other constituents:
isotonic sodium chloride solution.
According to experience, Functional disorders of the male gonads, conditioned by disease or old
to be administered in age, climacterium virile, sexual adynamia, sexual asthenia, hypogenitalism;
cases of: adjuvant for cellular regeneration therapy.
Characteristics: Chrysocor
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to foreign
protein.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 2 ml ampule 10 and 50 5X.
48
Citrokehl
Ampules
Liquid dilution for injection
Active ingredient: Acidum citricum 10X/30X/200X
Composition: 1 ampule of 2 ml contains: Medically active substance: 671 mg Acidum
citricum 10X aquous dil., 671 mg Acidum citricum 30X aquous
dil., 671 mg Acidum citricum 200X aquous dil. Other constituents:
isotonic sodium chloride solution.
According to experience, Allergic and rheumatic diseases; pneumonia and other respiratory dis-
to be administered in orders; arterial and venous diseases, arteriosclerosis; general symptoms,
cases of: e.g. tiredness, weather sensitivities, atypical headaches; gastrointestinal
dysfunction, cholangitis, dysbacteriosis, gastrointestinal complaints;
as adjuvant in pancreatic insufciency; disorder of the acid-alkaline-
balance.
Characteristics: Acidum citricum (citric acid), the active ingredient of Citrokehl
,
is an important link in the physiological citric acid cycle. It activates
cellular respiration and is of particular importance for cell metabolism.
Therefore, Citrokehl
Drops
Liquid dilution
for oral intake
Active ingredient: Acidum citricum 10X/30X/200X
Composition: 100 ml liquid dilution contains: Medically active substance: 33.4 ml
Acidum citricum 10X dil., 33.4 ml Acidum citricum 30X dil., 33.4
ml Acidum citricum 200X dil. Other constituents: puried water,
ethanol.
According to experience, Allergic and rheumatic diseases; pneumonia and other respiratory dis-
to be administered in orders; arterial and venous diseases, arteriosclerosis; general symptoms,
cases of: e.g. tiredness, weather sensitivities, atypical headaches; gastrointestinal
dysfunction, cholangitis, dysbacteriosis, gastrointestinal complaints;
as adjuvant in pancreatic insufciency; disorder of the acid-alkaline-
balance.
Characteristics: Acidum citricum (citric acid), the active ingredient of Citrokehl
,
is an important link in the physiological citric acid cycle. It activates
cellular respiration and is of particular importance for cell metabolism.
Therefore, Citrokehl
Tablets
for oral intake
Active ingredient: Acidum citricum 10X/30X/200X
Composition: 1 tablet contains: Medically active substance: 83.34 mg Acidum
citricum 10X trit., 83.34 mg Acidum citricum 30X trit., 83.34
mg Acidum citricum 200X trit. Other constituents: lactose, potato
starch, magnesium stearate.
According to experience, Allergic and rheumatic diseases; pneumonia and other respiratory dis-
to be administered in orders; arterial and venous diseases, arteriosclerosis; general symptoms,
cases of: e.g. tiredness, weather sensitivities, atypical headaches; gastrointestinal
dysfunction, cholangitis, dysbacteriosis, gastrointestinal complaints;
as adjuvant in pancreatic insufciency; disorder of the acid-alkaline-
balance.
Characteristics: Acidum citricum (citric acid), the active ingredient of Citrokehl
,
is an important link in the physiological citric acid cycle. It activates
cellular respiration and is of particular importance for cell metabolism.
Therefore, Citrokehl
3X
Drops
Liquid dilution for oral intake
Active ingredient: Cuprum gluconicum 3X
Composition: 10 ml liquid dilution contain: Medically active substance: 0.8 ml Cuprum
gluconicum 3X dil. Other constituents: puried water, ethanol 15 %
(m/m).
According to experience, Inammatory processes in the stomach, intestines and kidneys; pre- and
to be administered in postoperative phases.
cases of:
Characteristics: Copper is an essential trace element which is necessary in metabolism
for the function of diverse proteins and oxidative enzymes. It is
indispensable for the synthesis of hemoglobin, a healthy nerve function
and for bone formation. It also promotes the development of connective
tissue of the heart and circulatory system. Clinical situations which may
lead to a copper deciency are premature births, patients supplied
entirely with parenteral nutrition and children living on substandard
nutrition. The capacity of the granulocytes for phagocytosis and the
formation of immunoglobulins are decreased by copper deciency.
Application: Unless otherwise prescribed: For oral intake: in case of acute conditions
every half to one hour, not more than 6 times daily, each 5 drops. In case
of chronic conditions 1-3 x daily 5 drops.
Side effects: None known.
Contraindications: None known.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains 20 % (v/v) alcohol (ethanol). Due to the alcohol
content, professional medical advice should be sought prior to re-
commending this product to patients with alcohol or liver problems.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 30 ml dropper bottle 3X, 2 ml
ampule 10 and 50 4X.
52
Cuprukehl
4X
Ampules
Liquid dilution for injection
Active ingredient: Cuprum gluconicum 4X
Composition: 1 ampule of 2 ml contains: Medically active substance: 2 ml
Cuprum gluconicum 4X aquous dil. Other constituents: isotonic
sodium chloride solution.
According to experience, Inammatory processes in the stomach, intestines and kidneys; pre- and
to be administered in postoperative phases.
cases of:
Characteristics: Copper is an essential trace element which is necessary in metabolism
for the function of diverse proteins and oxidative enzymes. It is
indispensable for the synthesis of hemoglobin, a healthy nerve function
and for bone formation. It also promotes the development of connective
tissue of the heart and circulatory system. Clinical situations which may
lead to copper deciency are premature births, patients supplied entirely
with parenteral nutrition and children living on substandard nutrition.
The capacity of the granulocytes for phagocytosis and the formation of
immunoglobulins are decreased by copper deciency.
Application: Unless otherwise prescribed: 1 ampule of 2 ml to be injected either
intramuscularly, subcutaneously, intracutaneously or intravenously, 1-2
x daily.
Side effects: None known.
Contraindications: None known.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 30 ml dropper bottle 3X, 2 ml
ampule 10 and 50 4X.
53
Episcorit
Drops
Liquid dilution
for oral intake
Active ingredient: Concentrate of Echinacea purpurea with alcohol
Composition: 100 ml liquid dilution contain: Medically active substance: 75.6 ml
concentrate from fresh, blooming Echinacea purpurea herbs (1.5 -
2.5 : 1). Other constituents: ethanol.
According to experience, Support of treatment of recurrent infections of the respiratory and
to be administered in urinary tract.
cases of:
Characteristics: The origin of Echinacea purpurea is North America, where its wound
healing properties were preferred by the Indians. Echinacea stimulates
the production of endogenic interferon and therefore considerably
increases defensive mechanisms. Amongst others, they increase the
number of leucocytes and splenocytes.
Application: Unless otherwise prescribed: For oral intake: 3-4 x daily 55 drops.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Occasionally signs of a hypersensitivity reaction may occur. For drugs
containing Echinacea, symptoms like skin irritation, itching, facial
swelling, shortness of breath, dizziness, drop in blood pressure are
known. In this case, discontinue medication and treat symptomatically.
Contraindications: This preparation should not be administered if cases of hypersensitivity
against any of the ingredients, exipients or compositae are known.
Furthermore, it should not be administered in patients with progressive
systemic diseases such as tuberculosis, leucosis or similar diseases,
inammatory diseases of the connective tissue (collagenosis), multiple
sclerosis, AIDS, HIV infections, other chronic viral illnesses and
autoimmune diseases.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains 22 % (v/v) alcohol (ethanol).
Due to the alcohol content, professional medical advice should be
sought prior to recommending this product to patients with alcohol or
liver problems.
54
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 30 ml and 100 ml dropper
bottle.
55
Exmykehl
3X
Suppositories
for rectal application
Active ingredients: Candida albicans e volumine cellulae (lyophil., steril.) 3X,
Candida parapsilosis e volumine cellulae (lyophil., steril.) 3X,
Penicillium roquefortii e volumine cellulae (lyophil., steril.) 3X
Composition: 1 suppository contains: Medically active substances: 0.067 g Candida
albicans e volumine cellulae (lyophil., steril.) 3X trit., 0.067 g
Candida parapsilosis e volumine cellulae (lyophil., steril.)
3X trit., 0.067 g Penicillium roquefortii e volumine cellulae
(lyophil., steril.) 3X trit. Other constituents: hard fat, lactose.
According to experience, Intestinal mycosis, vaginal mycosis; prostate hypertrophy.
to be administered in
cases of:
Characteristics: Exmykehl
theoretically,
hypersensitivity may occur In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Candida albicans, Candida parapsilosis and Penicillium
roquefortii).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Exmykehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X.
56
Exmykehl
5X
Ampules
Liquid dilution for injection
Active ingredients: Candida albicans e volumine cellulae (lyophil., steril.) 5X,
Candida parapsilosis e volumine cellulae (lyophil., steril.) 5X,
Penicillium roquefortii e volumine cellulae (lyophil., steril.)
5X
Composition: 1 ampule of 1 ml contains: Medically active substances: 0.334 ml
Candida albicans e volumine cellulae (lyophil., steril.) 5X
aquous dil., 0.334 ml Candida parapsilosis e volumine cellulae
(lyophil., steril.) 5X aquous dil., 0.334 ml Penicillium roquefortii
e volumine cellulae (lyophil., steril.) 5X aquous dil. Other
constituents: isotonic sodium chloride solution.
According to experience, Intestinal mycosis, vaginal mycosis; prostate hypertrophy.
to be administered in
cases of:
Characteristics: Exmykehl
theoretically,
hypersensitivity may occur In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Candida albicans, Candida parapsilosis and Penicillium
roquefortii).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Exmykehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X.
57
Exmykehl
5X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredients: Candida albicans e volumine cellulae (lyophil., steril.) 5X,
Candida parapsilosis e volumine cellulae (lyophil., steril.) 5X,
Penicillium roquefortii e volumine cellulae (lyophil., steril.)
5X
Composition: 10 ml liquid dilution contain: Medically active substance: 3.34 ml
Candida albicans e volumine cellulae (lyophil., steril.) 5X dil.,
3.34 ml Candida parapsilosis e volumine cellulae (lyophil.,
steril.) 5X dil, 3.34 ml Penicillium roquefortii e volumine cellulae
(lyophil., steril.) 5X dil. Other constituents: puried water.
According to experience, Intestinal mycosis, vaginal mycosis; prostate hypertrophy.
to be administered in
cases of:
Characteristics: Exmykehl
theoretically,
hypersensitivity may occur In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Candida albicans, Candida parapsilosis and Penicillium
roquefortii).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Exmykehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X.
58
Fomepikehl
5X
Ampules
Liquid dilution for injection
Active ingredient: Fomitopsis pinicola extractum e volumine ex muris cellulae
(lyophil., steril.) 5X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml
Fomitopsis pinicola extractum e volumine ex muris cellulae
5X aquous dil. Other constituents: isotonic sodium chloride solution.
According to experience, Intermittent, remittent and bilious fever with headache, yellow tongue,
to be administered in constant nausea, weakness in the upper abdomen and constipation;
cases of: prostate adenoma.
Characteristics: Polysaccarid extracts from Fomitopsis pinicola prove to be highly
effective immune modulators. They also have vasodilatory and
hypotensive properties.
Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected subcuta-
neously, 1-3 x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Fomepikehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Fomitopsis
pinicola.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Fomepikehl
.
with other remedies:
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X.
59
Fomepikehl
5X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Fomitopsis pinicola extractum e volumine ex muris cellulae
(lyophil., steril.) 5X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml
Fomitopsis pinicola extractum e volumine ex muris cellulae
(lyophil., steril.) 5X dil. Other constituents: puried water.
According to experience, Intermittent, remittent and bilious fever with headache, yellow tongue,
to be administered in constant nausea, weakness in the upper abdomen and constipation;
cases of: prostate adenoma.
Characteristics: Polysaccarid extracts from Fomitopsis pinicola prove to be highly
effective immune modulators. They also have vasodilatory and
hypotensive properties.
Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Fomepikehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Fomitopsis
pinicola.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Fomepikehl
.
with other remedies:
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X.
60
Formasan
Ampules
Liquid dilution for injection
Active ingredient: Acidum formicicum 6X/12X/30X/200X
Composition: 1 ampule of 2 ml contains: Medically active substance: 0.5 ml Acidum
formicicum 6X aquous dil., 0.5 ml Acidum formicicum 12X
aquous dil., 0.5 ml Acidum formicicum 30X aquous dil., 0.5 ml
Acidum formicicum 200X aquous dil. Other constituents: isotonic
sodium chloride solution.
According to experience, Rheumatism of the muscles and joints; eczema; bronchial asthma,
to be administered in allergies.
cases of:
Characteristics: Acidum formicicum (formic acid), the active ingredient of Formasan
,
is traditionally used in folk medicine as embrocation in cases of
arthrosis, arthritis and rheumatism. Todays priority is the treatment of
rheumatic diseases with allergic diathesis. In homeopathy, ant acid is a
highly effective constitutional preparation for uric acid, rheumatic and
allergic conditions.
Application: Unless otherwise prescribed: 1 ampule of 2 ml to be injected intra-
muscularly or subcutaneously, 1-3 x weekly.
Side effects: None known.
Contraindications: None known.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 100 ml dropper bottle 6X/12X/
30X/200X potency mixture, 2 ml ampule 10 and 50 6X/12X/30X/200X
potency mixture.
61
Formasan
6X/12X/30X/200X
Drops
Liquid dilution for oral intake
Active ingredient: Acidum formicicum 6X/12X/30X/200X
Composition: 1 ml liquid dilution contains: Medically active substance: 0.25 ml Acidum
formicicum 6X dil., 0.25 ml Acidum formicicum 12X dil., 0.25 ml
Acidum formicicum 30X dil., 0.25 ml Acidum formicicum 200X
dil. Other constituents: Other constituents: puried water, ethanol.
According to experience, Rheumatism of the muscles and joints; eczema; bronchial asthma;
to be administered in allergies.
cases of:
Characteristics: Acidum formicicum (formic acid), the active ingredient of Formasan
,
is traditionally used in folk medicine as embrocation in cases of
arthrosis, arthritis and rheumatism. Todays priority is the treatment of
rheumatic diseases with allergic diathesis. In homeopathy, ant acid is a
highly effective constitutional preparation for uric acid, rheumatic and
allergic conditions.
Application: Unless otherwise prescribed: For oral intake: 1-3 x daily 5-20 drops.
Side effects: None known.
Contraindications: This product contains 50.6 % (v/v) alcohol (ethanol). This may present
a health risk in cases of liver diseases, alcoholism, epilepsy, brain
damage, pregnancy, and in children. The action of other drugs may be
reduced or intensied.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains 50.6 % (v/v) alcohol (ethanol).
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 100 ml dropper bottle 6X/12X/
30X/200X potency mixture, 2 ml ampule 10 and 50 6X/12X/30X/200X
potency mixture.
62
Fortakehl
3X
Suppositories
for rectal application
Active ingredient: Penicillium roquefortii e volumine cellulae (lyophil., steril.) 3X
Composition: 1 suppository contains: Medically active substance: 0.2 g Penicillium
roquefortii e volumine cellulae (lyophil., steril.) 3X trit. Other
constituents: hard fat, lactose.
According to experience, Dysbacteria and destroyed mucosa, gastritis, enteritis, colitis syndrome
to be administered in, pancreatitis, diarrhea, constipation, vomitus, gastric ulcer; mycoses of the
cases of: intestine, the vagina and the skin; bronchitis, susceptibility to
infections.
Characteristics: Fortakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Penicillium roquefortii).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Fortakehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
Penicillium roquefortii as an active ingredient is also contained in
Exmykehl
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1
ml ampule 10 and 50 5X, 6X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.
63
Fortakehl
4X
Capsules
for oral intake
Active ingredient: Penicillium roquefortii e volumine cellulae (lyophil., steril.) 4X
Composition: 1 capsule contains: Medically active substance: 330 mg Penicillium
roquefortii e volumine cellulae (lyophil., steril.) 4X trit. Other
constituents: lactose, hypromellosis (capsule shell).
According to experience, Dysbacteria and destroyed mucosa, gastritis, enteritis, colitis syndrome,
to be administered in pancreatitis, diarrhea, constipation, vomitus, gastric ulcer; mycoses of the
cases of: intestine, the vagina and the skin; bronchitis, susceptibility to infections.
Characteristics: Fortakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Penicillium roquefortii).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Fortakehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
Penicillium roquefortii as an active ingredient is also contained in
Exmykehl
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1
ml ampule 10 and 50 5X, 6X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.
64
Fortakehl
5X
Ampules
Liquid dilution for injection
Active ingredient: Penicillium roquefortii e volumine cellulae (lyophil., steril.) 5X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Penicillium
roquefortii e volumine cellulae (lyophil., steril.) 5X aquous dil.
Other constituents: isotonic sodium chloride solution.
According to experience, Dysbacteria and destroyed mucosa, gastritis, enteritis, colitis syndrome,
to be administered in pancreatitis, diarrhea, constipation, vomitus, gastric ulcer; mycoses of the
cases of: intestine, the vagina and the skin; bronchitis, susceptibility to
infections.
Characteristics: Fortakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Penicillium roquefortii).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Fortakehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: Penicillium roquefortii as an active ingredient is also contained in
Exmykehl
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1
ml ampule 10 and 50 5X, 6X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.
65
Fortakehl
5X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Penicillium roquefortii e volumine cellulae (lyophil., steril.) 5X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml
Penicillium roquefortii e volumine cellulae (lyophil., steril.)
5X dil. Other constituents: puried water.
According to experience, Dysbacteria and destroyed mucosa, gastritis, enteritis, colitis syndrome,
to be administered in pancreatitis, diarrhea, constipation, vomitus, gastric ulcer; mycoses of
cases of: the intestine, the vagina and the skin; bronchitis, susceptibility to
infections.
Characteristics: Fortakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Penicillium roquefortii).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Fortakehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: After opening, contents must be used within two months. Penicillium
roquefortii as an active ingredient is also contained in Exmykehl
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1
ml ampule 10 and 50 5X, 6X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.
66
Fortakehl
5X
Tablets
for oral intake
Active ingredient: Penicillium roquefortii e volumine cellulae (lyophil., steril.) 5X
Composition: 1 tablet contains: Medically active substance: 250 mg Penicillium
roquefortii e volumine cellulae (lyophil., steril.) 5X trit. Other
constituents: lactose, potato starch, magnesium stearate.
According to experience, Dysbacteria and destroyed mucosa, gastritis, enteritis, colitis syndrome,
to be administered in pancreatitis, diarrhea, constipation, vomitus, gastric ulcer; mycoses of
cases of: the intestine, the vagina and the skin; bronchitis, susceptibility to
infections.
Characteristics: Fortakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Penicillium roquefortii).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Fortakehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
Penicillium roquefortii as an active ingredient is also contained in
Exmykehl
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1
ml ampule 10 and 50 5X, 6X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.
67
Fortakehl
6X
Ampules
Liquid dilution for injection
Active ingredient: Penicillium roquefortii e volumine cellulae (lyophil., steril.) 6X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Penicillium
roquefortii e volumine cellulae (lyophil., steril.) 6X aquous dil.
Other constituents: isotonic sodium chloride solution.
According to experience, Dysbacteria and destroyed mucosa, gastritis, enteritis, colitis syndrome,
to be administered in pancreatitis, diarrhea, constipation, vomitus, gastric ulcer; mycoses of
cases of: the intestine, the vagina and the skin; bronchitis, susceptibility to
infections.
Characteristics: Fortakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Penicillium roquefortii).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Fortakehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: Penicillium roquefortii as an active ingredient is also contained in
Exmykehl
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1
ml ampule 10 and 50 5X, 6X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.
68
Ginkgobakehl
1X
Drops
Liquid dilution
for oral intake
Active ingredient: Ginkgo biloba e foliis sicc. mother tincture
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Ginkgo
biloba e foliis sicc. 1X dil. Other constituents: puried water, ethanol
62.4 % (m/m).
According to experience, According to the homeopathic drug picture, e.g. circulatory disorders
to be administered in (arterial and peripheral), arteriosclerosis; weakness in concentration,
cases of: tiredness.
Characteristics: In China Ginkgo preparations are known for treatment of various
diseases such as circulating disorders, various toxic burdens since
3,000 years B.C.
Application: Unless otherwise prescribed: For oral intake: 3-5 x daily 10-15 drops.
Side effects: Because of specic organic components of Ginkgobakehl
, theo-
retically, hypersensitivity may occur. In this case, discontinue medication
and treat symptomatically.
In very rare cases the following symptoms were observed: gastrointestinal
complaints, fever, headaches or allergic skin reactions (reddening,
swelling, itching). In cases of long-term treatment occasionally bleeding
occurred, however, a causal link to the intake of Ginkgo preparations
has not been veried.
Contraindications: This product contains 70 % (v/v) alcohol (ethanol). Following the dosage
recommendations, 15 drops lead to an alcohol intake of 0.2 g. This may
present a health risk in cases of liver diseases, alcoholism, epilepsy,
brain damage, pregnancy, and in children. The action of other drugs
may be reduced or intensied.
Adverse reactions: None known.
Interactions The action of anticoagulants may be intensied. Please note that this also
with other remedies: applies to intake a few hours or days before.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains 70 % (v/v) alcohol (ethanol).
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 30 ml dropper bottle 1X, 4X,
2 ml ampule 10 and 50 4X.
69
Ginkgobakehl
4X
Ampules
Liquid dilution for injection
Active ingredient: Ginkgo biloba e foliis sicc. 4X
Composition: 1 ampule of 2 ml contains: Medically active substance: 2 ml Ginkgo
biloba e foliis sicc. 4X aquous dil. Other constituents: isotonic
sodium chloride solution.
According to experience, According to the homeopathic drug picture, e.g. circulatory disorders
to be administered in (arterial and peripheral), arteriosclerosis; weakness in concentration,
cases of: tiredness.
Characteristics: In China Ginkgo preparations are known for treatment of various
diseases such as circulating disorders, various toxic burdens since
3,000 years B.C.
Application: Unless otherwise prescribed: 1 ampule of 2 ml to be injected either
intramuscularly, subcutaneously, intracutaneously or intravenously, 1 x
daily.
Side effects: Because of specic organic components of Ginkgobakehl
, theo-
retically, hypersensitivity may occur. In this case, discontinue medication
and treat symptomatically.
In very rare cases the following symptoms were observed: gastrointestinal
complaints, fever, headaches or allergic skin reactions (reddening,
swelling, itching). In cases of long-term treatment occasionally bleeding
occurred, however, a causal link to the intake of Ginkgo preparations
has not been veried.
Contraindications: Do not administer in cases of known hypersensitivity to Ginkgo biloba.
Adverse reactions: None known.
Interactions The action of anticoagulants may be intensied. Please note that this
with other remedies: also applies to intake a few hours or days before.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 30 ml dropper bottle 1X, 4X,
2 ml ampule 10 and 50 4X.
70
Ginkgobakehl
4X
Drops
Liquid dilution
for oral intake
Active ingredient: Ginkgo biloba e foliis sicc. 4X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Ginkgo
biloba e foliis sicc. 4X dil. Other constituents: puried water, ethanol
42.4 % (m/m).
According to experience, According to the homeopathic drug picture, e.g. circulatory disorders
to be administered in (arterial and peripheral), arteriosclerosis; weakness in concentration,
cases of: tiredness.
Characteristics: In China Ginkgo preparations are known for treatment of various
diseases such as circulating disorders, various toxic burdens since
3,000 years B.C.
Application: Unless otherwise prescribed: For oral intake: 3-5 x daily 10-15 drops.
Side effects: Because of specic organic components of Ginkgobakehl
, theo-
retically, hypersensitivity may occur. In this case, discontinue medication
and treat symptomatically.
In very rare cases the following symptoms were observed: gastrointestinal
complaints, fever, headaches or allergic skin reactions (reddening,
swelling, itching). In cases of long-term treatment occasionally bleeding
occurred, however, a causal link to the intake of Ginkgo preparations
has not been veried.
Contraindications: This product contains 50 % (v/v) alcohol (ethanol). Following the dosage
recommendations, 15 drops lead to an alcohol intake of 0.2 g. This may
present a health risk in cases of liver diseases, alcoholism, epilepsy,
brain damage, pregnancy, and in children. The action of other drugs
may be reduced or intensied.
Adverse reactions: None known.
Interactions The action of anticoagulants may be intensied. Please note that this
with other remedies: also applies to intake a few hours or days before.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains 50 % (v/v) alcohol (ethanol).
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 30 ml dropper bottle 1X, 4X,
2 ml ampule 10 and 50 4X.
71
Grifokehl
5X
Ampules
Liquid dilution for injection
Active ingredient: Grifola frondosa e volumine cellulae (lyophil., steril.) 5X
Composition: 1 ampule of 1 ml contains:: Medically active substance: 10 ml Grifola
frondosa e volumine cellulae (lyophil., steril.) 5X dil. Other
constituents: isotonic sodium chloride solution.
According to experience, Immune modulation, Herpes simplex, Herpes zoster.
to be administered in
cases of:
Characteristics: Grifokehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Grifola
frondosa.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X.
72
Grifokehl
5X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Grifola frondosa e volumine cellulae (lyophil., steril.) 5X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Grifola
frondosa e volumine cellulae (lyophil., steril.) 5X dil. Other
constituents: puried water.
According to experience, Immune modulation, Herpes simplex, Herpes zoster.
to be administered in
cases of:
Characteristics: Grifokehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Grifola
frondosa.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X.
73
Hexacyl
Drops
Liquid dilution
for oral intake
Active ingredients: Sulphur 4X dilution, Lycopodium clavatum mother tincture,
Berberis vulgaris mother tincture
Composition: 10 g (corresponds to 10.99 ml) liquid dilution contains: Medically active
substance: 3.00 g Sulphur 4X dil, 0.10 g Lycopodium clavatum
mother tincture, 0.05 g Berberis vulgaris mother tincture.
Other constituents:, ethanol 43% (m/m), puried water.
Indication Supporting treatment for functional liver, gallbladder and kidney
disorders.
Characteristics: The active ingredients of Hexacyl
- Sulphur, Lycopodium clavatum
and Berberis vulgaris - present a similar range of action in their
homeopathic drug picture. Each of the single substances shows
symptoms of venous stasis in the circulatory system which results in
disturbances of other organs, in particular of the liver and kidneys.
Leading symptoms are: Severe burning and itching, exhaustion;
deterioration by heat, cold and rest; improvement through fresh air and
moderate movement. Hexacyl
, theoretically,
hypersensitivity may occur. In this case, discontinue use and treat
symptomatically.
Contraindications: This product contains 59.9 % (v/v) alcohol (ethanol). This may present
a health risk in cases of liver diseases, alcoholism, epilepsy, brain
damage, pregnancy, and in children. The action of other drugs may be
reduced or intensied.
Adverse reactions: None known.
Interactions,
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains 59.9 % (v/v) alcohol (ethanol).
74
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage form is available: 30 ml dropper bottle.
75
Larikehl
4X
Capsules
for oral intake
Active ingredient: Laricifomes ofcinalis e volumine cellulae (lyophil., steril.)
4X
Composition: 1 capsule contains: Medically active substance: 330 mg Laricifomes
ofcinalis e volumine cellulae (lyophil., steril.) 4X trit. Other
constituents: lactose, hypromellosis (capsule shell).
According to experience, Fever, lung diseases and inammation of the digestive organs; primary
to be administered in chronic polyarthritis.
cases of:
Characteristics: Larikehl
, theoretically,
hypersensitivity may occur, mainly in the form of skin reactions. Also
allergic reactions against the ingredient Laricifomes ofcinalis
are possible. In this case, discontinue medication and treat sympto-
matically.
Contraindications: Do not administer in cases of known hypersensitivity to Laricifomes
ofcinalis.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of with other
remedies: Larikehl
5X
Ampules
Liquid dilution for injection
Active ingredient: Laricifomes ofcinalis e volumine cellulae (lyophil., steril.)
5X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Laricifomes
ofcinalis e volumine cellulae (lyophil., steril.) 5X aquous dil.
Other constituents: isotonic sodium chloride solution.
According to experience, Fever, lung diseases and inammation of the digestive organs; primary
to be administered in chronic polyarthritis.
cases of:
Characteristics: Larikehl
, theoretically,
hypersensitivity may occur, mainly in the form of skin reactions. Also
allergic reactions against the ingredient Laricifomes ofcinalis
are possible. In this case, discontinue medication and treat sympto-
matically.
Contraindications: Do not administer in cases of known hypersensitivity to Laricifomes
ofcinalis.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Larikehl
.
with other remedies: An interval of 4 weeks before and after the treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 20 capsules 4X.
77
Larikehl
5X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Laricifomes ofcinalis e volumine cellulae (lyophil., steril.)
5X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml
Laricifomes ofcinalis e volumine cellulae (lyophil., steril.)
5X dil. Other constituents: puried water.
According to experience, Fever, lung diseases and inammation of the digestive organs; primary
to be administered in chronic polyarthritis.
cases of:
Characteristics: Larikehl
, theoretically,
hypersensitivity may occur, mainly in the form of skin reactions. Also
allergic reactions against the ingredient Laricifomes ofcinalis
are possible. In this case, discontinue medication and treat sympto-
matically.
Contraindications: Do not administer in cases of known hypersensitivity to Laricifomes
ofcinalis.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Larikehl
.
with other remedies: An interval of 4 weeks before and after the treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 20 capsules 4X.
78
Latensin
4X
Ampules
Liquid dilution for injection
Active ingredient: Bacillus cereus e volumine cellulae (lyophil. steril.) 4X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Bacillus
cereus e volumine cellulae (lyophil., steril.) 4X aquous dil. Other
constituents: isotonic sodium chloride solution.
According to experience, Chronic inammation of the respiratory and digestive tract; chronic
to be administered in rheumatic disorders; chronic skin diseases; susceptibility to infection
cases of: (for immune modulation).
Characteristics: Latensin
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
Do not administer in cases of known hypersensitivity to Bacillus
cereus.
Adverse reactions: None known. Generally well tolerated. Occasionally local reactions
like rubefaction, swelling or painfulness may be observed, normally
vanishing without treatment. These effects are not to be seen as
adverse reactions, but rather as an expression of effectiveness. In the
rst 2 or 3 days after the injection sometimes conditions of weakness,
fortied expectoration, slight painfulness of the region or subfebrile
temperatures may show. Strong general reactions are always a sign of
overdose or of incorrect injection technique.
Interactions Immunosuppressive drugs can inuence the effectivity of Latensin
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X,6X.
79
Latensin
4X
Capsules
for oral intake
Active ingredient: Bacillus cereus e volumine ex muris cellulae (lyophil., steril.)
4X
Composition: 1 capsule contains: Medically active substance: 330 mg Bacillus
cereus e volumine ex muris cellulae (lyophil., steril.) 4X trit.
Other constituents: lactose, hypromellosis (capsule shell).
According to experience, Chronic inammation of the respiratory and digestive tract; chronic
to be administered in rheumatic disorders; chronic skin diseases; susceptibility to infection
cases of: (for immune modulation).
Characteristics: Latensin
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
Do not administer in cases of known hypersensitivity to Bacillus
cereus.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions Immunosuppressive drugs can inuence the effectivity of Latensin
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X,6X.
80
Latensin
6X
Ampules
Liquid dilution for injection
Active ingredient: Bacillus cereus e volumine cellulae (lyophil., steril.) 6X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Bacillus
cereus e volumine cellulae (lyophil., steril.) 6X aquous dil. Other
constituents: isotonic sodium chloride solution.
According to experience, Chronic inammation of the respiratory and digestive tract; chronic
to be administered in rheumatic disorders; chronic skin diseases; susceptibility to infection
cases of: (for immune modulation).
Characteristics: Latensin
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
Do not administer in cases of known hypersensitivity to Bacillus
cereus.
Adverse reactions: None known. Generally well tolerated. Occasionally local reactions
like rubefaction, swelling or painfulness may be observed, normally
vanishing without treatment. These effects are not to be seen as
adverse reactions, but rather as an expression of effectiveness. In the
rst 2 or 3 days after the injection sometimes conditions of weakness,
fortied expectoration, slight painfulness of the region or subfebrile
temperatures may show. Strong general reactions are always a sign of
overdose or of incorrect injection technique.
Interactions Immunosuppressive drugs can inuence the effectivity of Latensin
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X,6X.
81
Latensin
6X
Capsules
for oral intake
Active ingredient: Bacillus cereus e volumine ex muris cellulae (lyophil., steril.)
6X
Composition: 1 capsule contains: Medically active substance: 330 mg Bacillus
cereus e volumine ex muris cellulae (lyophil., steril.) 6X trit.
Other constituents: lactose, hypromellosis (capsule shell).
According to experience, Chronic inammation of the respiratory and digestive tract; chronic
to be administered in rheumatic disorders; chronic skin diseases; susceptibility to infection
cases of: (for immune modulation).
Characteristics: Latensin
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
Do not administer in cases of known hypersensitivity to Bacillus
cereus.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions Immunosuppressive drugs can inuence the effectivity of Latensin
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.
82
Latensin
6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Bacillus cereus e volumine cellulae (lyophil., steril.) 6X
Composition: 5 ml liquid dilution contain: Medically active substance: 5 ml Bacillus
cereus e volumine cellulae (lyophil., steril.) 6X dil. Other
constituents: puried water.
According to experience, Chronic inammation of the respiratory and digestive tract; chronic
to be administered in rheumatic disorders; chronic skin diseases; susceptibility to infection
cases of: (for immune modulation).
Characteristics: Latensin
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
Do not apply to inamed skin. Do not administer in cases of known
hypersensitivity to Bacillus cereus.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions Immunosuppressive drugs can inuence the effectivity of Latensin
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.
83
Latensin
6X
Suppositories
for rectal application
Active ingredient: Bacillus cereus e volumine ex muris cellulae (lyophil., steril.) 6X
Composition: 1 suppository contains: Medically active substance: 0.2 g Bacillus
cereus e volumine ex muris cellulae (lyophil., steril.) 6X trit.
Other constituents: hard fat, lactose.
According to experience, Chronic inammation of the respiratory and digestive tract; chronic
to be administered in rheumatic disorders; chronic skin diseases; susceptibility to infection
cases of: (for immune modulation).
Characteristics: Latensin
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
Do not administer in cases of known hypersensitivity to Bacillus
cereus.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions Immunosuppressive drugs can inuence the effectivity of Latensin
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.
84
Leptospermusan 1X
Drops
Liquid dilution
for oral intake
Active ingredient: Leptospermum scoparium e apic. ramorum siccum 1X
Composition: 1 ml liquid dilution contain: Medically active substance: 1 ml
Leptospermum scoparium e apic. ramorum siccum 1X dil.
Other constituents: puried water, ethanol.
According to experience, Secondary effects of apoplexy, ischaemic attack; inammations such as
to be administered in trigeminal neuralgia, iritis, allergic conjunctivitis; diseases of the respiratory
cases of: tract such as cold and sore throat; for a general soothing inuence;
sleep disorder; cell renewal; gastrointestinal diseases such as gastritis,
pylorospasm, constipation, colitis.
Characteristics: Leptospermum scoparium or manuka is a wild growing bush
found in New Zealand and is well known in Polynesian folk medicine.
Preparations from its leaves, bark and seed pods were used for
treating different diseases, but especially for dysentery and diarrhoea.
As with other species of the myrtles, Leptospermum scoparium
contains essential oils, well known for their antibacterial activity.
Anthelmintic properties of Leptospermum have been reported.
Further pharmacological effective constituents are tannins as well as
rare avonoids.
Application: Unless otherwise prescribed: in case of acute conditions 5 drops every
half to full hour up to a maximum of 12 times daily. In case of chronic
conditions 5 drops up to 3 times daily.
Side effects: Because of specic organic components of Leptospermusan,
theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.
Contraindications: This product contains 70 % (v/v) alcohol (ethanol). This may present
a health risk in cases of liver diseases, alcoholism, epilepsy, brain
damage, pregnancy, and in children. The action of other drugs may be
reduced or intensied.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains 70 % (v/v) alcohol (ethanol).
85
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 30 ml dropper bottle 1X.
86
Leptucin
6X
Capsules
for oral intake
Active ingredient: Propionibacterium avidum e volumine ex muris cellulae
(lyophil., steril.) 6X
Composition: 1 capsule contains: Medically active substance: 330 mg Propioni-
bacterium avidum e volumine ex muris cellulae (lyophil.,
steril.) 6X trit. Other constituents: lactose, hypromellosis (capsule
shell).
According to experience, Stimulation of circulation of the extremities; vascular migraine; tinnitus;
to be administered in inammation of the urinary bladder; immune modulation.
cases of:
Characteristics: Propionibacteria belong to the strongest immune modulators. Due
to the special structure of their cell wall they are able to stimulate
the immune system by activation of the monocyte-macrophage-
system. They have antibacterial, antiviral, antiparasitic, and antitumor
properties. Moreover, Leptucin
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Propioni-
bacterium avidum.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions Immunosuppressive drugs can inuence the effectivity of Leptucin
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 20 capsules 6X, 10
suppositories 6X.
87
Leptucin
6X
Suppositories
for rectal application
Active ingredient: Propionibacterium avidum e volumine ex muris cellulae
(lyophil., steril.) 6X
Composition: 1 suppository contains: Medically active substance: 0.2 g Bacillus
subtilis e volumine ex muris cellulae cellulae (lyophil., steril.)
6X trit. Other constituents: hard fat, lactose.
According to experience, Stimulation of circulation of the extremities; vascular migraine; tinnitus;
to be administered in inammation of the urinary bladder; immune modulation.
cases of:
Characteristics: Propionibacteria belong to the strongest immune modulators. Due
to the special structure of their cell wall they are able to stimulate
the immune system by activation of the monocyte-macrophage-
system. They have antibacterial, antiviral, antiparasitic, and antitumor
properties. Moreover, Leptucin
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Propioni-
bacterium avidum.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions Immunosuppressive drugs can inuence the effectivity of Leptucin
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 20 capsules 6X, 10
suppositories 6X.
88
Lipiscor
Capsules
for oral intake
Active ingredient: Piscis oleum (polyunsaturated fatty acids from sea sh)
Composition: 1 Capsule contains: Medically active substance: 500 mg Piscis
oleum (polyunsaturated fatty acids from sea sh) containing
70 mg icosapent and 50 mg doconexent. Other constituents: RRR-a-
tocopherol, al-rac-a-tocopherolum acetate, gelatin, glycerol, puried
water.
Indication: To lower a highly increased triglyceride blood level. Lipiscor
should
only be administered additionally if a diet is insufcient in lowering
triglyceride.
Characteristics: Lipiscor
contains natural sh oil with a high content of essential
polyunsaturated omega-3-(n-3) fatty acids, which are icosapent
(eicosapentaenoic acid) and doconexent (docosahexaenoic acid).
The results of epidemiological studies on populations such as Innuits,
Japanese, Dutch and Americans show a correlation between a high
intake of sea sh and a low appearance of cardiovascular diseases. The
regular intake of Lipiscor
leads to a lowering of plasma triglycerides
within four weeks. If taken on a permanent basis the triglyceride
level will remain constant. If discontinued, the plasma triglycerides
will return to their former level within 2-3 months. The omega-3 fatty
acids contained in Lipiscor
go into the normal lipid metabolism,
particularly the metabolism of eicosanoids and prostaglandins. The
lipid-lowering effect of Lipiscor
is probably the result of an inhibition
of the triglyceride synthesis. Taking Lipiscor
increases the proportion
of omega-3-(n-3) fatty acids.
Application: Unless otherwise prescribed: 5-10 capsules twice daily. Lipiscor
is to
be swallowed unchewed with some liquid before a meal.
Side effects: High dosages may occasionally cause nausea and eructation. Lipiscor
may prolong bleeding time and inhibit platelet aggregation. A modest
increase in transaminases is possible.
Contraindications: Acute and subacute pancreatitis, acute pancreas necrosis, acute and
chronic liver intoxications, cirrhosis of the liver from all origins, acute
to chronic cholecystitis, suppuration of the gall bladder, disorders of
digestion as well as emulsication of fat in the small intestine due to
diseases of the gallbladder and/or pancreas, thrombopathia, if allergic
reactions against any of the ingredients are known.
Because Lipiscor
may cause a delay of uterine contractions it should
not be administered in the last 3 months of pregnancy.
Adverse reactions: In case of bronchial asthma which is sensitive to salicylic acid a
deterioration of the lung function may occur.
89
Interactions Since Lipiscor
prolongs bleeding time and may reduce the platelet
with other remedies: aggregation, patients with thrombopenia and patients who are treated
with anticoagulant drugs should be under constant medical supervision
as it might be necessary to reduce the administration of anticoagulant
drugs.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children or in case of hypercholesterinaemia.
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health careprofessional.
How supplied: The following dosage forms are available: 60 and 240 capsules.
90
Luffasan
4X
Tablets
for oral intake
Active ingredient: Luffa operculata 4X
Composition: 1 tablet contains: Medically active substance: 250 mg Luffa oper-
culata 4X trit. Other constituents: lactose, potato starch, magnesium
stearate.
Indication: Hay fever, cold; headache, dyspepsia.
Characteristics: Luffasan
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Luffa oper-
culata.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 80 tablets 4X.
91
Mapurit
L
Capsules
for oral intake
Active ingredients: Magnesium oxide, vitamin E
Composition: 1 capsule contains: 208,4 mg magnesium oxide, 123,5 mg vitamin E
(as RRR-alpha-tocopherylhydrogensuccinat). Other constituents: hypro-
mellose, cellulose, magnesiumstearat.
From experience Reduced endogenous resistibility, especially chronic exhaustion.
to administer for:
Characteristics: Magnesium deciency is an important diet-related cause for the
development of chronic exhaustion. To compensate, magnesium oxide
should be administered which has a membrane-stabilizing effect on all
cell membranes and cell organelle membranes. The metabolism of carbo-
hydrates, proteins and lipids as well as the excitation metabolism of
nerves and muscles are positively affected.
Application: Recommended dose: 1 capsule twice a day.
How supplied: Package with 40/100 capsules.
92
Mucedokehl
3X
Suppositories
for rectal application
Active ingredient: Mucor mucedo (+) / (-) e volumine cellulae (lyophil., steril.)
3X
Composition: 1 suppository contains: Medically active substance: 0.2 g Mucor
mucedo (+) / (-) volumine cellulae (lyophil., steril.) 3X trit. Other
constituents: hard fat, lactose.
According to experience, Neuro-vegetative syndrome, regulatory dysfunctions in the limbic system,
to be administered in anxiety, depression; respiratory diseases, sinusitis, tonsillitis, sino-
cases of: bronchitis; ostitis; lymphostasis; thyroidal disorders.
Characteristics: Mucedokehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Mucor mucedo).
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.
93
Mucedokehl
4X
Capsules
for oral intake
Active ingredient: Mucor mucedo (+) / (-) e volumine cellulae (lyophil., steril.)
4X
Composition: 1 capsule contains: Medically active substance: 330 mg Mucor
mucedo (+) / (-) e volumine cellulae (lyophil., steril.) 4X trit.
Other constituents: lactose, hypromellosis (capsule shell).
According to experience, Neuro-vegetative syndrome, regulatory dysfunctions in the limbic system,
to be administered in anxiety, depression; respiratory diseases, sinusitis, tonsillitis, sino-
cases of: bronchitis; ostitis; lymphostasis; thyroidal disorders.
Characteristics: Mucedokehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Mucor mucedo).
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.
94
Mucedokehl
5X
Ampules
Liquid dilution for injection
Active ingredient: Mucor mucedo (+) / (-) e volumine cellulae (lyophil., steril.)
5X
Composition: 1 ampule of 1 ml contains:: Medically active substance: 10 ml Mucor
mucedo (+) / (-) e volumine cellulae (lyophil., steril.) 5X dil.
Other constituents: isotonic sodium chloride solution.
According to experience, Neuro-vegetative syndrome, regulatory dysfunctions in the limbic system,
to be administered in anxiety, depression; respiratory diseases, sinusitis, tonsillitis, sino-
cases of: bronchitis; ostitis; lymphostasis; thyroidal disorders.
Characteristics: Mucedokehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Mucor mucedo).
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.
95
Mucedokehl
5X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Mucor mucedo (+) / (-) e volumine cellulae (lyophil., steril.)
5X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Mucor
mucedo (+) / (-) e volumine cellulae (lyophil., steril.) 5X dil.
Other constituents: puried water.
According to experience, Neuro-vegetative syndrome, regulatory dysfunctions in the limbic system,
to be administered in anxiety, depression; respiratory diseases, sinusitis, tonsillitis, sino-
cases of: bronchitis; ostitis; lymphostasis; thyroidal disorders.
Characteristics: Mucedokehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Mucor mucedo).
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.
96
Mucokehl
3X
Ointment
for rubbing in
Active ingredient: Mucor racemosus e volumine cellulae (lyophil., steril.) 3X
Composition: 1 g ointment contains: Medically active substance: 0.1 g Mucor
racemosus e volumine cellulae (lyophil., steril.) 3X dil. Other
constituents: 0.38 g lanolin alcohol ointment, 0.10 g coconut oil fract.,
0.03 g glyceryl monostearate 40-55%, 0.23 g propylene glycol, 0.02
g magnesium sulphate x 7 H2O, 0.01 g lactic acid, 0.13 g water for
injection.
According to experience, Diseases of the veins and their disturbed circulation such as varicosis,
to be administered in thrombophlebitis, hemorrhoids; generally for inammatory diseases;
cases of: swellings, contusions, distortions, ischialgia, chronic pain syndrome;
cicatricial keloids, chronic dermatitis, neurodermatitis; ovarian und tubal
cysts (locally on the lower abdomen); tentatively in cases of Dupuytrens
contracture and exion contracture.
Characteristics: In Isopathy Mucokehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Mucor racemosus).
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Additional advice: Mucor racemosus as an active ingredient is also contained in
Sankombi
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X, 10 single use
vials eye drops 5X (preservative-free).
97
Mucokehl
3X
Suppositories
for rectal application
Active ingredient: Mucor racemosus e volumine cellulae (lyophil., steril.) 3X
Composition: 1 suppository contains: Medically active substance: 0.2 g Mucor
racemosus e volumine cellulae (lyophil., steril.) 3X trit. Other
constituents: hard fat, lactose.
According to experience, Chronic, latent and acute inrmities of the vascular system, such as
to be administered in thromboses embolism, post-infarct processes, angina pectoris, circulatory
cases of: disorders and disturbed healing of wounds, such as smokers leg,
diabetic gangrene, neurodermatitis, venous diseases, such as
varicosity, hemorrhoids, ssure ani; glaucoma; inammatory diseases
of the organs and the connective tissue in the small pelvis, such as
endometritis, prostatitis, colitis syndrome, diverticulitis, prostate
adenoma; precanceroses; lymphostasis; chronic pain syndrome.
Characteristics: In Isopathy Mucokehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Mucor racemosus).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Mucokehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
Additional advice: Mucor racemosus as an active ingredient is also contained in
Sankombi
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
98
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X, 10 single use
vials eye drops 5X (preservative-free).
99
Mucokehl
4X
Capsules
for oral intake
Active ingredient: Mucor racemosus e volumine cellulae (lyophil., steril.) 4X
Composition: 1 capsule contains: Medically active substance: 330 mg Mucor
racemosus e volumine cellulae (lyophil., steril.) 4X trit. Other
constituents: lactose, hypromellosis (capsule shell).
According to experience, Chronic, latent and acute inrmities of the vascular system, such as
to be administered in thromboses, embolism, post-infarct processes, angina pectoris, circu-
cases of: latory disorders and disturbed healing of wounds, such as smokers
leg, diabetic gangrene, neurodermatitis, venous diseases, such as
varicosity, hemorrhoids, ssure ani; glaucoma; inammatory diseases
of the organs and the connective tissue in the small pelvis, such as
endometritis, prostatitis, colitis syndrome, diverticulitis, prostate
adenoma; precanceroses; lymphostasis; chronic pain syndrome.
Characteristics: In Isopathy Mucokehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Mucor racemosus).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Mucokehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
Additional advice: Mucor racemosus as an active ingredient is also contained in
Sankombi
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
100
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X, 10 single use
vials eye drops 5X (preservative-free).
101
Mucokehl
5X
Ampules
Liquid dilution for injection
Active ingredient: Mucor racemosus e volumine cellulae (lyophil., steril.) 5X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Mucor
racemosus e volumine cellulae (lyophil., steril.) 5X aquous dil.
Other constituents: isotonic sodium chloride solution.
According to experience, Chronic, latent and acute inrmities of the vascular system, such as
to be administered in thromboses, embolism, post-infarct processes, angina pectoris, circu-
cases of: latory disorders and disturbed healing of wounds, such as smokers
leg, diabetic gangrene, neurodermatitis, venous diseases, such as
varicosity, hemorrhoids, ssure ani; glaucoma; inammatory diseases
of the organs and the connective tissue in the small pelvis, such as
endometritis, prostatitis, colitis syndrome, diverticulitis, prostate
adenoma; precanceroses; lymphostasis; chronic pain syndrome.
Characteristics: In Isopathy Mucokehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Mucor racemosus).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Mucokehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Additional advice: Mucor racemosus as an active ingredient is also contained in
Sankombi
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
102
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X, 10 single use
vials eye drops 5X (preservative-free).
103
Mucokehl
5X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Mucor racemosus e volumine cellulae (lyophil., steril.) 5X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Mucor
racemosus e volumine cellulae (lyophil., steril.) 5X dil. Other
constituents: puried water.
According to experience, Chronic, latent and acute inrmities of the vascular system, such as
to be administered in thromboses, embolism, post-infarct processes, angina pectoris, circu-
cases of: latory disorders and disturbed healing of wounds, such as smokers
leg, diabetic gangrene, neurodermatitis, venous diseases, such as
varicosity, hemorrhoids, ssure ani; glaucoma; inammatory diseases
of the organs and the connective tissue in the small pelvis, such as
endometritis, prostatitis, colitis syndrome, diverticulitis, prostate
adenoma; precanceroses; lymphostasis; chronic pain syndrome.
Characteristics: In Isopathy Mucokehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Mucor racemosus).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Mucokehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: After opening, contents must be used within two months.
Additional advice: Mucor racemosus as an active ingredient is also contained in
Sankombi
.
104
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X , 10 single use
vials eye drops 5X (preservative-free).
105
Mucokehl
5X
Eye drops
Liquid dilution for the eyes
Active ingredient: Mucor racemosus e volumine cellulae (lyophil., steril.) 5X
Composition: 5 ml liquid dilution contains: Medically active substance: 4.999.95 mg
Mucor racemosus e volumine cellulae (lyophil., steril.) 5X dil.
Other constituents: isotonic sodium chloride solution, 0.05 mg
chlorohexidinediacetate.
According to experience, Glaucoma, cataract, conjunctivitis, dry eye syndrome.
to be administered in
cases of:
Characteristics: In Isopathy Mucokehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: In cases of known hypersensitivity to Mucor racemosus, as a
precaution, this preparation should not be administered.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: To avoid contamination, do not touch tip of dropper to any surface. This
remedy should be used within one month of opening.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X, 10 single use
vials eye drops 5X (preservative-free).
106
Mucokehl
5X
Eye drops in single use vials (preservative-free)
Liquid dilution for the eyes
Active ingredient: Mucor racemosus e volumine cellulae (lyophil., steril.) 5X
Composition: 1 single use vial contains: Medically active substance per 0.017 oz / 0.5 ml
vial: 0.05 mg Mucor racemosus e volumine cellulae (lyophil.,
steril.) 5X dil. Other constituents: water, salt.
According to experience, Glaucoma, cataract, conjunctivitis, dry eye syndrome.
to be administered in
cases of:
Characteristics: In Isopathy Mucokehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: In cases of known hypersensitivity to Mucor racemosus, as a
precaution, this preparation should not be administered.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: To avoid contamination, do not touch tip of vial to any surface. Do not
use if vial is broken or damaged. Use vials up before the expiry date or
before the expiration of 6 months after opening the bag and within 24
hours after opening the vial.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X, 10 single use
vials eye drops 5X (preservative-free).
107
Mucokehl
5X
Tablets
for oral intake
Active ingredient: Mucor racemosus e volumine cellulae (lyophil., steril.) 5X
Composition: 1 tablet contains: Medically active substance: 250 mg Mucor race-
mosus e volumine cellulae (lyophil., steril.) 5X trit. Other
constituents: lactose, potato starch, magnesium stearate.
According to experience, Chronic, latent and acute inrmities of the vascular system, such as
to be administered in thromboses, embolism, post-infarct processes, angina pectoris, circu-
cases of: latory disorders and disturbed healing of wounds, such as smokers
leg, diabetic gangrene, neurodermatitis, venous diseases, such as
varicosity, hemorrhoids, ssure ani; glaucoma; inammatory diseases
of the organs and the connective tissue in the small pelvis, such as
endometritis, prostatitis, colitis syndrome, diverticulitis, prostate
adenoma; precanceroses; lymphostasis; chronic pain syndrome.
Characteristics: In Isopathy Mucokehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Mucor racemosus).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Mucokehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
Additional advice: Mucor racemosus as an active ingredient is also contained in
Sankombi
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
108
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X, 10 single use
vials eye drops 5X (preservative-free).
109
Mucokehl
6X
Ampules
Liquid dilution for injection
Active ingredient: Mucor racemosus e volumine cellulae (lyophil., steril.) 6X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Mucor
racemosus e volumine cellulae (lyophil., steril.) 6X aquous dil.
Other constituents: isotonic sodium chloride solution.
According to experience, Chronic, latent and acute inrmities of the vascular system, such as
to be administered in thromboses, embolism, post-infarct processes, angina pectoris, circu-
cases of: latory disorders and disturbed healing of wounds, such as smokers
leg, diabetic gangrene, neurodermatitis, venous diseases, such as
varicosity, hemorrhoids, ssure ani; glaucoma; inammatory diseases
of the organs and the connective tissue in the small pelvis, such as
endometritis, prostatitis, colitis syndrome, diverticulitis, prostate
adenoma; precanceroses; lymphostasis; chronic pain syndrome.
Characteristics: In Isopathy Mucokehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Mucor racemosus).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Mucokehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Additional advice: Mucor racemosus as an active ingredient is also contained in
Sankombi
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
110
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X, 10 single use
vials eye drops 5X (preservative-free).
111
Mucokehl
7X
Ampules
Liquid dilution for injection
Active ingredient: Mucor racemosus e volumine cellulae (lyophil., steril.) 7X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Mucor
racemosus e volumine cellulae (lyophil., steril.) 7X aquous dil.
Other constituents: isotonic sodium chloride solution.
According to experience, Chronic, latent and acute inrmities of the vascular system, such as
to be administered in thromboses, embolism, post-infarct processes, angina pectoris, circu-
cases of: latory disorders and disturbed healing of wounds, such as smokers
leg, diabetic gangrene, neurodermatitis, venous diseases, such as
varicosity, hemorrhoids, ssure ani; glaucoma; inammatory diseases
of the organs and the connective tissue in the small pelvis, such as
endometritis, prostatitis, colitis syndrome, diverticulitis, prostate
adenoma; precanceroses; lymphostasis; chronic pain syndrome.
Characteristics: In Isopathy Mucokehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Mucor racemosus).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Mucokehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Additional advice: Mucor racemosus as an active ingredient is also contained in
Sankombi
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
112
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X, 10 single use
vials eye drops 5X (preservative-free).
113
Mucokehl
Atox 6X
Ampules
Liquid dilution for injection
Active ingredient: Mucor racemosus serum oryctolagi (steril.) 6X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml rabbit
serum 6X dil., derived from rabbits that were pre-treated with Mucor
racemosus 2X/3X dil. Other constituents: isotonic sodium chloride
solution.
According to experience, Elimination after application of Mucokehl
.
to be administered in
cases of:
Characteristics: Mucokehl
Atox 6X,
theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,
especially rabbit protein.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: To be administered 1 day after Mucokehl
at the earliest.
Drink plenty of uids.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.
114
Mucokehl
Atox 6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Mucor racemosus serum oryctolagi (steril.) 6X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml rabbit
serum 6X dil., derived from rabbits that were pre-treated with Mucor
racemosus 2X/3X dil. Other constituents: puried water.
According to experience, Elimination after application of Mucokehl
.
to be administered in
cases of:
Characteristics: Mucokehl
Atox 6X,
theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,
especially rabbit protein.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: After opening, contents must be used within two months.
To be administered 1 day after Mucokehl
at the earliest.
Drink plenty of uids.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.
115
Muscarsan
6X
Ampules
Liquid dilution for injection
Active ingredient: Amanita muscaria e thallo 6X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Amanita
muscaria e thallo 6X aquous dil. Other constituents: isotonic sodium
chloride solution.
According to experience, Detoxication in case of drug and medication abuse; cerebral ischaemic
to be administered in attack; nervous and cerebral hyperexcitability; spasms of muscles, organs
cases of: and blood vessels, migraine; nervous disorders of the intestine.
Characteristics: The Amanita muscaria fungus is known for its characteristic
appearance and toxicity. The occurring symptoms after the consumption
of dried y agaric are similar to those which arise after drug abuse.
Amanita muscaria is applied for therapeutic purposes in homeopathy
whereby the range of application is relatively broad. Important areas of
application are cerebral and nervous overexcitement and exhaustion
conditions, headache with pupils or students, cerebral circulatory
disorders, vertigo, intoxicated and ecstatic conditions, muscular and
organic spasms, migraine and vascular spasms, nervous disorders
of the intestinal tract, gastralgia, meteorism, chronic fermentative
dyspepsia, damage from coffee and tabacco, alcoholism, drug and
tablet abuse.
Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either
intramuscularly, subcutaneously or intracutaneously 1-3x weekly.
Side effects: Because of specic organic components of Muscarsan
,
theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Amanita
muscaria.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X, 80 tablets 6X.
116
Muscarsan
6X
Drops
Liquid dilution for oral intake
Active ingredient: Amanita muscaria e thallo 6X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Amanita
muscaria e thallo 6X dil. Other constituents: puried water, ethanol.
According to experience, Detoxication in case of drug and medication abuse; cerebral ischaemic
to be administered in attack; nervous and cerebral hyperexcitability; spasms of muscles,
cases of: organs and blood vessels, migraine; nervous disorders of the intestine.
Characteristics: The Amanita muscaria fungus is known for its characteristic
appearance and toxicity. The occurring symptoms after the consumption
of dried y agaric are similar to those which arise after drug abuse.
Amanita muscaria is applied for therapeutic purposes in homeopathy
whereby the range of application is relatively broad. Important areas of
application are cerebral and nervous overexcitement and exhaustion
conditions, headache with pupils or students, cerebral circulatory
disorders, vertigo, intoxicated and ecstatic conditions, muscular and
organic spasms, migraine and vascular spasms, nervous disorders
of the intestinal tract, gastralgia, meteorism, chronic fermentative
dyspepsia, damage from coffee and tabacco, alcoholism, drug and
tablet abuse.
Application: Unless otherwise prescribed:
For oral intake: 1 x daily 5-10 drops.
Side effects: Because of specic organic components of Muscarsan
,
theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Amanita
muscaria.
This product contains 50 % (v/v) alcohol (ethanol). Following the dosage
recommendations, 5 drops lead to an alcohol intake of 0.05 g. This may
present a health risk in cases of liver diseases, alcoholism, epilepsy,
brain damage, pregnancy, and in children. The action of other drugs
may be reduced or intensied.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
117
Advice: This product contains 50 % (v/v) alcohol (ethanol).
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X, 80 tablets 6X.
118
Muscarsan
6X
Tablets
for oral intake
Active ingredient: Amanita muscaria e thallo 6X
Composition: 1 tablet contains: Medically active substance: 250 mg Amanita mus-
caria e thallo 6X trit. Other constituents: lactose, potato starch,
magnesium stearate.
According to experience, Detoxication in case of drug and medication abuse; cerebral ischaemic
to be administered in attack; nervous and cerebral hyperexcitability; spasms of muscles, organs
cases of: and blood vessels, migraine; nervous disorders of the intestine.
Characteristics: The Amanita muscaria fungus is known for its characteristic
appearance and toxicity. The occurring symptoms after the consumption
of dried y agaric are similar to those which arise after drug abuse.
Amanita muscaria is applied for therapeutic purposes in homeopathy
whereby the range of application is relatively broad. Important areas of
application are cerebral and nervous overexcitement and exhaustion
conditions, headache with pupils or students, cerebral circulatory
disorders, vertigo, intoxicated and ecstatic conditions, muscular and
organic spasms, migraine and vascular spasms, nervous disorders
of the intestinal tract, gastralgia, meteorism, chronic fermentative
dyspepsia, damage from coffee and tabacco, alcoholism, drug and
tablet abuse.
Application: Unless otherwise prescribed: 1-3 x daily 1 tablet.
Side effects: Because of specic organic components of Muscarsan
,
theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Amanita
muscaria.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X, 80 tablets 6X.
119
Nigersan
3X
Suppositories
for rectal application
Active ingredient: Aspergillus niger e volumine cellulae (lyophil., steril.) 3X
Composition: 1 suppository contains: Medically active substance: 0.2 g Aspergillus
niger e volumine cellulae (lyophil., steril.) 3X trit. Other consti-
tuents: hard fat, lactose.
According to experience, Diseases of the urogenital tract, such as myoma, cysts, prostate adenoma;
to be administered in degenerative or inammatory conditions, such as Scheuermann disease,
cases of: Perthes disease and Bechterews disease; disorders of the respiratory
tract; lymphatism; goiter diseases; obesity; verrucae (warts).
Characteristics: Nigersan
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Aspergillus niger).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Nigersan
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
Additional advice: Aspergillus niger as an active ingredient is also contained in
Sankombi
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.
120
Nigersan
4X
Capsules
for oral intake
Active ingredient: Aspergillus niger e volumine cellulae (lyophil., steril.) 4X
Composition: 1 capsule contains: Medically active substance: 330 mg Aspergillus
niger e volumine cellulae (lyophil., steril.) 4X trit. Other consti-
tuents: lactose, hypromellosis (capsule shell).
According to experience, Diseases of the urogenital tract, such as myoma, cysts, prostate adenoma;
to be administered in degenerative or inammatory conditions, such as Scheuermann disease,
cases of: Perthes disease and Bechterews disease; disorders of the respiratory
tract; lymphatism; goiter diseases; obesity; verrucae (warts).
Characteristics: Nigersan
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Aspergillus niger).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Nigersan
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
Additional advice: Aspergillus niger as an active ingredient is also contained in
Sankombi
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.
121
Nigersan
5X
Ampules
Liquid dilution for injection
Active ingredient: Aspergillus niger e volumine cellulae (lyophil., steril.) 5X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Aspergillus
niger e volumine cellulae (lyophil., steril.) 5X aquous dil. Other
constituents: isotonic sodium chloride solution.
According to experience, Diseases of the urogenital tract, such as myoma, cysts, prostate adenoma;
to be administered in degenerative or inammatory conditions, such as Scheuermann disease,
cases of: Perthes disease and Bechterews disease; disorders of the respiratory
tract; lymphatism; goiter diseases; obesity; verrucae (warts).
Characteristics: Nigersan
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Aspergillus niger).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Nigersan
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Additional advice: Aspergillus niger as an active ingredient is also contained in
Sankombi
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.
122
Nigersan
5X
Drops
Liquid dilution
for oral intake, rubbing in, inhalation
Active ingredient: Aspergillus niger e volumine cellulae (lyophil., steril.) 5X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml
Aspergillus niger e volumine cellulae (lyophil., steril.) 5X dil.
Other constituents: puried water.
According to experience, Diseases of the urogenital tract, such as myoma, cysts, prostate adenoma;
to be administered in degenerative or inammatory conditions, such as Scheuermann disease,
cases of: Perthes disease and Bechterews disease; disorders of the respiratory
tract; lymphatism; goiter diseases; obesity; verrucae (warts).
Characteristics: Nigersan
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Aspergillus niger).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Nigersan
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: After opening, contents must be used within two months.
Additional advice: Aspergillus niger as an active ingredient is also contained in
Sankombi
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.
123
Nigersan
5X
Tablets
for oral intake
Active ingredient: Aspergillus niger e volumine cellulae (lyophil., steril.) 5X
Composition: 10 tablet contains: Medically active substance: 250 mg Aspergillus
niger e volumine cellulae (lyophil., steril.) 5X trit. Other consti-
tuents: lactose, potato starch, magnesium stearate.
According to experience, Diseases of the urogenital tract, such as myoma, cysts, prostate adenoma;
to be administered in degenerative or inammatory conditions, such as Scheuermann disease,
cases of: Perthes disease and Bechterews disease; disorders of the respiratory
tract; lymphatism; goiter diseases; obesity; verrucae (warts).
Characteristics: Nigersan
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Aspergillus niger).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Nigersan
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
Additional advice: Aspergillus niger as an active ingredient is also contained in
Sankombi
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.
124
Nigersan
6X
Ampules
Liquid dilution for injection
Active ingredient: Aspergillus niger e volumine cellulae (lyophil., steril.) 6X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Aspergillus
niger e volumine cellulae (lyophil., steril.) 6X aquous dil. Other
constituents: isotonic sodium chloride solution.
According to experience, Diseases of the urogenital tract, such as myoma, cysts, prostate adenoma;
to be administered in degenerative or inammatory conditions, such as Scheuermann disease,
cases of: Perthes disease and Bechterews disease; disorders of the respiratory
tract; lymphatism; goiter diseases; obesity; verrucae (warts).
Characteristics: Nigersan
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Aspergillus niger).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Nigersan
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: None.
Additional advice: Aspergillus niger as an active ingredient is also contained in
Sankombi
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.
125
Nigersan
7X
Ampules
Liquid dilution for injection
Active ingredient: Aspergillus niger e volumine cellulae (lyophil., steril.) 7X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Aspergillus
niger e volumine cellulae (lyophil., steril.) 7X aquous dil. Other
constituents: isotonic sodium chloride solution.
According to experience, Diseases of the urogenital tract, such as myoma, cysts, prostate adenoma;
to be administered in degenerative or inammatory conditions, such as Scheuermann disease,
cases of: Perthes disease and Bechterews disease; disorders of the respiratory
tract; lymphatism; goiter diseases; obesity; verrucae (warts).
Characteristics: Nigersan
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Aspergillus niger).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Nigersan
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: None.
Additional advice: Aspergillus niger as an active ingredient is also contained in
Sankombi
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.
126
Nigersan
Atox 6X
Ampules
Liquid dilution for injection
Active ingredient: Aspergillus niger serum oryctolagi (steril.) 6X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml rabbit serum
6X dil., derived from rabbits that were pre-treated with Aspergillus
niger 2X/3X dil. Other constituents: isotonic sodium chloride
solution.
According to experience, Elimination after application of Nigersan
.
to be administered in
cases of:
Characteristics: Nigersan
Atox 6X is a highly effective preparation for supporting
elimination of metabolic and decomposition products, especially after
application of Nigersan
Atox 6X,
theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,
especially rabbit protein.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: To be administered 1 day after Nigersan
at the earliest.
Drink plenty of uids.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.
127
Nigersan
Atox 6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Aspergillus niger serum oryctolagi (steril.) 6X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml
rabbit serum 6X dil., derived from rabbits that were pre-treated with
Aspergillus niger 2X/3X dil. Other constituents: puried water.
According to experience, Elimination after application of Nigersan
.
to be administered in
cases of:
Characteristics: Nigersan
Atox 6X is a highly effective preparation for supporting
elimination of metabolic and decomposition products, especially after
application of Nigersan
Atox 6X,
theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,
especially rabbit protein.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: After opening, contents must be used within two months.
To be administered 1 day after Nigersan
at the earliest.
Drink plenty of uids.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.
128
Notakehl
3X
Ointment
for rubbing in
Active ingredient: Penicillium chrysogenum e volumine cellulae (lyophil., steril.) 3X
Composition: 1 g ointment contains: Medically active substance: 0.1 g Penicillium
chrysogenum e volumine cellulae (lyophil., steril.) 3X dil. Other
constituents: 0.38 g lanolin alcohol ointment, 0.10 g coconut oil fract.,
0.03 g glyceryl monostearate 40-55%, 0.23 g propylene glycol, 0.02 g
magnesium sulphate x 7 H2O, 0.01 g lactic acid, 0.13 g water for injection.
According to experience, Bacterial disorders, e.g. tonsillitis, laryngitis, otitis; diseases of the
to be administered in urogenital system, such as cystitis, prostatitis, endometriosis; respiratory
cases of: diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis; neuritis,
neuralgia, cervical spine and lumbar spine syndrome; suppurations,
acne, after tooth extractions.
Characteristics: Notakehl
is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damages, destruction
of intestinal ora and the formation of Penicillin resistant strains.
Application: Unless otherwise prescribed: Apply thinly on the affected area 1 to 3 x
daily.
Side effects: Because of specic organic components of Notakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Penicillium chrysogenum).
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Additional advice: Penicillium chrysogenum as an active ingredient is also contained
in Nota-Quent.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X.
129
Notakehl
3X
Suppositories
for rectal application
Active ingredient: Penicillium chrysogenum e volumine cellulae (lyophil., steril.) 3X
Composition: 1 suppository contains: Medically active substance: 0.2 g Penicillium
chrysogenum e volumine cellulae (lyophil., steril.) 3X trit. Other
constituents: hard fat, lactose.
According to experience, Bacterial disorders, e.g. tonsillitis, laryngitis, otitis; diseases of the
to be administered in urogenital system, such as cystitis, prostatitis, endometriosis; respiratory
cases of: diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis; neuritis,
neuralgia, cervical spine and lumbar spine syndrome; suppurations,
acne, after tooth extractions.
Characteristics: Notakehl
is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damages, destruction
of intestinal ora and the formation of Penicillin resistant strains.
Application: Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Notakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Penicillium chrysogenum).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Notakehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
Additional advice: Penicillium chrysogenum as an active ingredient is also contained
in Nota-Quent.
130
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X.
131
Notakehl
4X
Capsules
for oral intake
Active ingredient: Penicillium chrysogenum e volumine cellulae (lyophil., steril.) 4X
Composition: 1 capsule contains: Medically active substance: 330 mg Penicillium
chrysogenum e volumine cellulae (lyophil., steril.) 4X trit. Other
constituents: lactose, hypromellosis (capsule shell).
According to experience, Bacterial disorders, e.g. tonsillitis, laryngitis, otitis; diseases of the
to be administered in urogenital system, such as cystitis, prostatitis, endometriosis; respiratory
cases of: diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis; neuritis,
neuralgia, cervical spine and lumbar spine syndrome; suppurations,
acne, after tooth extractions.
Characteristics: Notakehl
is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damages, destruction
of intestinal ora and the formation of Penicillin resistant strains.
Application: Unless otherwise prescribed: 1-3 x daily 1 capsule.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Notakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Penicillium chrysogenum).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Notakehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
Additional advice: Penicillium chrysogenum as an active ingredient is also contained
in Nota-Quent.
Duration of treatment: Dependent on the advice of the physician or health care professional.
132
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X.
133
Notakehl
5X
Ampules
Liquid dilution for injection
Active ingredient: Penicillium chrysogenum e volumine cellulae (lyophil., steril.) 5X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Penicillium
chrysogenum e volumine cellulae (lyophil., steril.) 5X aquous
dil. Other constituents: isotonic sodium chloride solution.
According to experience, Bacterial disorders, e.g. tonsillitis, laryngitis, otitis; diseases of the
to be administered in urogenital system, such as cystitis, prostatitis, endometriosis; respiratory
cases of: diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis; neuritis,
neuralgia, cervical spine and lumbar spine syndrome; suppurations,
acne, after tooth extractions.
Characteristics: Notakehl
is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damages, destruction
of intestinal ora and the formation of Penicillin resistant strains.
Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either
intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3 x
weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Notakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Penicillium chrysogenum).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Notakehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Additional advice: Penicillium chrysogenum as an active ingredient is also contained
in Nota-Quent.
Duration of treatment: Dependent on the advice of the physician or health care professional.
134
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X.
135
Notakehl
5X
Drops
Liquid dilution
for oral intake, rubbing in, inhalation
Active ingredient: Penicillium chrysogenum e volumine cellulae (lyophil., steril.) 5X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml
Penicillium chrysogenum e volumine cellulae (lyophil., steril.)
5X dil. Other constituents: puried water.
According to experience, Bacterial disorders, e.g. tonsillitis, laryngitis, otitis; diseases of the
to be administered in urogenital system, such as cystitis, prostatitis, endometriosis; respiratory
cases of: diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis; neuritis,
neuralgia, cervical spine and lumbar spine syndrome; suppurations,
acne, after tooth extractions.
Characteristics: Notakehl
is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damages, destruction
of intestinal ora and the formation of Penicillin resistant strains.
Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops.
For rubbing in: 1 x daily 5-10 drops into the bend of the elbow. For
inhalation: 10-20 drops, inhaled deeply 2-3 x daily.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Notakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Penicillium chrysogenum).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Notakehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: After opening, contents must be used within two months.
Additional advice: Penicillium chrysogenum as an active ingredient is also contained
in Nota-Quent.
136
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X.
137
Notakehl
5X
Tablets
for oral intake
Active ingredient: Penicillium chrysogenum e volumine cellulae (lyophil., steril.) 5X
Composition: 1 tablet contains: Medically active substance: 250 mg Penicillium
chrysogenum e volumine cellulae (lyophil., steril.) 5X trit. Other
constituents: lactose, potato starch, magnesium stearate.
According to experience, Bacterial disorders, e.g. tonsillitis, laryngitis, otitis; diseases of the
to be administered in urogenital system, such as cystitis, prostatitis, endometriosis; respiratory
cases of: diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis; neuritis,
neuralgia, cervical spine and lumbar spine syndrome; suppurations,
acne, after tooth extractions.
Characteristics: Notakehl
is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damages, destruction
of intestinal ora and the formation of Penicillin resistant strains.
Application: Unless otherwise prescribed: 1-3 x daily 1 tablet.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Notakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Penicillium chrysogenum).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Notakehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
Additional advice: Penicillium chrysogenum as an active ingredient is also contained
in Nota-Quent.
138
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X.
139
Notakehl
6X
Ampules
Liquid dilution for injection
Active ingredient: Penicillium chrysogenum e volumine cellulae (lyophil., steril.) 6X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Penicillium
chrysogenum e volumine cellulae (lyophil., steril.) 6X aquous
dil. Other constituents: isotonic sodium chloride solution.
According to experience, Bacterial disorders, e.g. tonsillitis, laryngitis, otitis; diseases of the
to be administered in urogenital system, such as cystitis, prostatitis endometriosis; respiratory
cases of: diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis; neuritis,
neuralgia, cervical spine and lumbar spine syndrome; suppurations,
acne, after tooth extractions.
Characteristics: Notakehl
is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damages, destruction
of intestinal ora and the formation of Penicillin resistant strains.
Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either
intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3 x
weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Notakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Penicillium chrysogenum).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Notakehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: None.
Additional advice: Penicillium chrysogenum as an active ingredient is also contained
in Nota-Quent.
140
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X.
141
Notakehl
7X
Ampules
Liquid dilution for injection
Active ingredient: Penicillium chrysogenum e volumine cellulae (lyophil., steril.) 7X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Penicillium
chrysogenum e volumine cellulae (lyophil., steril.) 7X aquous
dilut. Other constituents: isotonic sodium chloride solution.
According to experience, Bacterial disorders, e.g. tonsillitis, laryngitis, otitis; diseases of the
to be administered in urogenital system, such as cystitis, prostatitis endometriosis; respiratory
cases of: diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis; neuritis,
neuralgia, cervical spine and lumbar spine syndrome; suppurations,
acne, after tooth extractions.
Characteristics: Notakehl
is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damages, destruction
of intestinal ora and the formation of Penicillin resistant strains.
Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either
intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3 x
weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Notakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Penicillium chrysogenum).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Notakehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: None.
Additional advice: Penicillium chrysogenum as an active ingredient is also contained
in Nota-Quent.
142
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X.
143
Nota-Quent 5X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredients: Penicillium chrysogenum e volumine cellulae (lyophil., steril.)
5X, Penicillium glabrum e volumine cellulae (lyophil., steril.) 5X
Composition: 10 ml liquid dilution contain: Medically active substance: 5 ml
Penicillium chrysogenum e volumine cellulae (lyophil., steril.)
5X dil., 5 ml Penicillium glabrum e volumine cellulae (lyophil.,
steril.) 5X dil. Other constituents: puried water.
According to experience, All acute and latent diseases caused by mixed bacterial and viral in-
to be administered in fections, such as tonsillitis, laryngitis, bronchitis, sinusitis, otitis, in-
cases of: uenzal infections, asthma-bronchitis, bronchitis, sino-bronchitis; neuritis,
neuralgia; diseases of the urogenital system, such as cystitis, prostatitis,
endometriosis.
Characteristics: Nota-Quent is a combination of two specic preparations: Penicillium
chrysogenum and Penicillium glabrum. It is not an antibiotic and
does not produce antibiotic substances. Therefore, there are no side
effects like those which may occur during treatment with antibiotics,
such as allergies, liver damages, destruction of intestinal ora and the
formation of Penicillin resistant strains.
Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.
Side effects: Because of specic organic components of Nota-Quent, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Penicillium chrysogenum and Penicillium glabrum).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Nota-Quent.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage form is available: 10 ml dropper bottle 5X.
144
Okoubasan
2X
Drops
Liquid dilution
for oral intake
Active ingredient: Okoubaka aubrevillei 2X
Composition: 1 ml liquid dilution contains: Medically active substance: 1 ml Okoubaka
aubrevillei 2X dil. Other constituents: puried water, ethanol.
According to experience, Acute diarrhea, especially after food poisoning, infections of the gastro-
to be administered in intestinal tract, food intolerances, prophylactically in cases of change of
cases of nutrition and climate; during a regulation therapy for elimination of
metabolic waste products.
Characteristics: Okoubasan
,
theoretically, hypersensitivity may occur. In this case, discontinue use
and treat symptomatically.
Contraindications: This product contains 70 % (v/v) alcohol (ethanol). This may present
a health risk in cases of liver diseases, alcoholism, epilepsy, brain
damage, pregnancy, and in children. The action of other drugs may be
reduced or intensied.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains 70 % (v/v) alcohol (ethanol).
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 2X, 80
tablets 2X.
145
Okoubasan
2X
Tablets
for oral intake
Active ingredient: Okoubaka aubrevillei 2X
Composition: 1 tablet contains: Medically active substance: 250 mg Okoubaka
aubrevillei 2X trit. Other constituents: lactose, potato starch,
magnesium stearate.
Indication: Acute diarrhea, especially after food poisoning, infections of the gastro-
intestinal tract, food intolerances, prophylactically in cases of change
of nutrition and climate; during a regulation therapy for elimination of
metabolic waste products.
Characteristics: Okoubasan
,
theoretically, hypersensitivity may occur. In this case, discontinue use
and treat symptomatically.
Contraindications: None known.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 2X, 80
tablets 2X.
146
Pefrakehl
3X
Ointment
for rubbing in
Active ingredient: Candida parapsilosis e volumine cellulae (lyophil., steril.) 3X
Composition: 1 g ointment contains: Medically active substance: 0.1 g Candida
parapsilosis e volumine cellulae (lyophil., steril.) 3X dil. Other
constituents: 0.38 g lanolin alcohol ointment, 0.10 g coconut oil fract.,
0.03 g glyceryl monostearate 40-55%, 0.23 g propylene glycol, 0.02
g magnesium sulphate x 7 H2O, 0.01 g lactic acid, 0.13 g water for
injection.
According to experience, Disorders of the respiratory tract; intestinal mycoses, secondary
to be administered in mycotic diseases of the skin and the mucous membranes; all bacterial
cases of: and viral diseases, such as rhagades, aphthae, pemphigus vulgaris,
lymphadenitis, cystitis, otitis externa, acne, dental granuloma.
Characteristics: Pefrakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Candida parapsilosis).
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: None.
Additional Advice: Candida parapsilosis as an active ingredient is also contained in
Exmykehl
.
147
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 6X, 10 suppositories 3X, 20 capsules 4X, 30 g tube
of ointment 3X.
148
Pefrakehl
3X
Suppositories
for rectal application
Active ingredient: Candida parapsilosis e volumine cellulae (lyophil., steril.) 3X
Composition: 1 suppository contains: Medically active substance: 0.2 g Candida
parapsilosis e volumine cellulae (lyophil., steril.) 3X trit. Other
constituents: hard fat, lactose.
According to experience, Disorders of the respiratory tract; intestinal mycoses, secondary
to be administered in mycotic diseases of the skin and the mucous membranes; all
cases of: bacterial and viral diseases, such as rhagades, aphthae, pemphigus
vulgaris, lymphadenitis, cystitis, otitis externa, acne, dental granuloma.
Characteristics: Pefrakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Candida parapsilosis).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Pefrakehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
Additional advice: Candida parapsilosis as an active ingredient is also contained in
Exmykehl
.
149
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 6X, 10 suppositories 3X, 20 capsules 4X, 30 g tube
of ointment 3X.
150
Pefrakehl
4X
Capsules
for oral intake
Active ingredient: Candida parapsilosis e volumine cellulae (lyophil., steril.) 4X
Composition: 1 capsule contains: Medically active substance: 330 mg Candida
parapsilosis e volumine cellulae (lyophil., steril.) 4X trit.
Other constituents: lactose, hypromellosis (capsule shell).
According to experience, Disorders of the respiratory tract; intestinal mycoses, secondary
to be administered in mycotic diseases of the skin and the mucous membranes; all bac-
cases of: terial and viral diseases, such as rhagades aphthae, pemphigus
vulgaris, lymphadenitis, cystitis, otitis externa, acne, dental granuloma.
Characteristics: Pefrakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Candida parapsilosis).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Pefrakehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
Additional advice: Candida parapsilosis as an active ingredient is also contained in
Exmykehl
.
151
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 6X, 10 suppositories 3X, 20 capsules 4X, 30 g tube
of ointment 3X.
152
Pefrakehl
5X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Candida parapsilosis e volumine cellulae (lyophil., steril.) 5X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Candida
parapsilosis e volumine cellulae (lyophil., steril.) 5X dil. Other
constituents: puried water.
According to experience, Disorders of the respiratory tract; intestinal mycoses, secondary
to be administered in mycotic diseases of the skin and the mucous membranes; all bacterial
cases of: and viral diseases, such as rhagades, aphthae, pemphigus vulgaris,
lymphadenitis, cystitis, otitis externa, acne, dental granuloma.
Characteristics: Pefrakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Candida parapsilosis).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Pefrakehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: After opening, contents must be used within two months.
153
Additional advice: Candida parapsilosis as an active ingredient is also contained in
Exmykehl
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 6X, 10 suppositories 3X, 20 capsules 4X, 30 g tube
of ointment 3X.
154
Pefrakehl
6X
Ampules
Liquid dilution for injection
Active ingredient: Candida parapsilosis e volumine cellulae (lyophil., steril.) 6X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Candida
parapsilosis e volumine cellulae (lyophil., steril.) 6X aquous dil.
Other constituents: isotonic sodium chloride solution.
According to experience, Disorders of the respiratory tract; intestinal mycoses, secondary mycotic
to be administered in diseases of the skin and the mucous membranes; all bacterial and
cases of: viral diseases, such as rhagades, aphthae, pemphigus vulgaris,
lymphadenitis, cystitis, otitis externa, acne, dental granuloma.
Characteristics: Pefrakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Candida parapsilosis).
Adverse reactions: None known.
Interactions
with other remedies: Immunosuppressive drugs can inuence the effectivity of Pefrakehl
.
An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: None.
155
Additional Advice: Candida parapsilosis as an active ingredient is also contained in
Exmykehl
.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 6X, 10 suppositories 3X, 20 capsules 4X, 30 g tube
of ointment 3X.
156
Pinikehl
4X
Capsules
for oral intake
Active ingredient: Fomitopsis pinicola e volumine cellulae (lyophil., steril.) 4X
Composition: 1 capsule contains: Medically active substance: 330 mg Fomitopsis
pinicola e volumine cellulae 4X trit. Other constituents: lactose
hypromellosis (capsule shell).
According to experience, Diseases of the liver and spleen, intermittent fever.
administered in
cases of:
Characteristics: Pinikehl
is produced from Fomitopsis pinicola and is preferably
administered in weakness and disorders of liver and spleen.
Application: Unless otherwise prescribed: 1-3 x daily 1 capsule.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Pinikehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Fomitopsis
pinicola.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Pinikehl
. An
with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.
157
Pinikehl
4X
Suppositories
for rectal application
Active ingredient: Fomitopsis pinicola e volumine cellulae (lyophil., steril.) 4X
Composition: 1 suppository contains: Medically active substance: 0.2 g Fomitopsis
pinicola e volumine cellulae (lyophil., steril.) 4X trit. Other
constituents: hard fat, lactose.
According to experience, Diseases of the liver and spleen, intermittent fever.
administered in
cases of:
Characteristics: Pinikehl
is produced from Fomitopsis pinicola and is preferably
administered in weakness and disorders of liver and spleen.
Application: Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Pinikehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Fomitopsis
pinicola.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Pinikehl
. An
with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.
158
Pinikehl
5X
Ampules
Liquid dilution for injection
Active ingredient: Fomitopsis pinicola e volumine cellulae (lyophil., steril.) 5X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Fomitopsis
pinicola e volumine cellulae 5X aquous dil. Other constituents:
isotonic sodium chloride
According to experience, Diseases of the liver and spleen, intermittent fever.
administered in
cases of:
Characteristics: Pinikehl
is produced from Fomitopsis pinicola and is preferably
administered in weakness and disorders of liver and spleen.
Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either
intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3x
weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Pinikehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Fomitopsis
pinicola.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Pinikehl
. An
with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.
159
Pinikehl
5X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Fomitopsis pinicola e volumine cellulae (lyophil., steril.) 5X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml
Fomitopsis pinicola e volumine cellulae (lyophil., steril.) 5X
dil. Other constituents: puried water.
According to experience, Diseases of the liver and spleen, intermittent fever.
administered in
cases of:
Characteristics: Pinikehl
is produced from Fomitopsis pinicola and is preferably
administered in weakness and disorders of liver and spleen.
Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Pinikehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Fomitopsis
pinicola.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Pinikehl
. An
with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.
160
Pleo Chelate
Drops
Liquid dilution
for oral intake
Active ingredients: Sodium edetate 2X, hydrogen peroxide 2X, magnesium
sulphate 2X, potassium chloride 2X, sodium chloride 2X
Composition: 100 g solution contains: Medically active substances: 8 g sodium
edetate 2X, 8 g hydrogen peroxide 2X, 4 g magnesium sulphate
2X, 4 g potassium chloride 2X, 1.6 g Sodium chloride 2X. Other
constituents: puried water, ethanol.
According to experience, Reduction of high burden with heavy metals (e.g. lead in the air, mercury
to be administered in in tooth llings, high levels of metals in drinking water, etc.).
cases of:
Characteristics: Pleo Chelate
administration.
Contraindications: Do not administer in cases of known hypersensitivity against sodium
edentate.
Do not administer during pregnancy.
Adverse reactions: None known.
161
Interactions Possible interference with chemotherapeutics, therefore, Pleo
Chelate
. Pleo Chelate
3X
Suppositories
for rectal application
Active ingredient: Penicillium glabrum e volumine cellulae (lyophil., steril.) 3X
Composition: 1 suppository contains: Medically active substance: 0.2 g Penicillium
glabrum e volumine cellulae (lyophil., steril.) 3X trit. Other
constituents: hard fat, lactose.
According to experience, Acute and latent viral infections, e.g. laryngitis, bronchitis, sinusitis, pharyn-
to be administered in gitis, inuenzal infections; all diseases caused by mixed caused by
cases of: mixed infections, e.g. Herpes zoster, chicken pox; migraine; multiple
sclerosis; vertigo; Menires disease.
Characteristics: Quentakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Penicillium glabrum).
Adverse reactions: None known.
Interactions
with other remedies: Immunosuppressive drugs can inuence the effectivity of Quentakehl
.
An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
183
Additional advice: Penicillium glabrum as an active ingredient is also contained in
Nota-Quent.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.
184
Quentakehl
4X
Capsules
for oral intake
Active ingredient: Penicillium glabrum e volumine cellulae (lyophil., steril.) 4X
Composition: 1 capsule contains: Medically active substance: 330 mg Penicillium
glabrum e volumine cellulae 4X trit. Other constituents: lactose,
hypromellosis (capsule shell).
According to experience, Acute and latent viral infections, e.g. laryngitis, bronchitis, sinusitis, pharyn-
to be administered in gitis, inuenzal infections; all diseases caused by mixed infections, e.g.
cases of: Herpes zoster, chicken pox; migraine; multiple sclerosis; vertigo;
Menires disease.
Characteristics: Quentakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Penicillium glabrum).
Adverse reactions: None known.
Interactions with
other remedies: Immunosuppressive drugs can inuence the effectivity of Quentakehl
.
An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
185
Additional advice: Penicillium glabrum as an active ingredient is also contained in
Nota-Quent.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.
186
Quentakehl
5X
Ampules
Liquid dilution for injection
Active ingredient: Penicillium glabrum e volumine cellulae (lyophil., steril.) 5X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Penicillium
glabrum e volumine cellulae (lyophil., steril.) 5X aquous dil.
Other constituents: isotonic sodium chloride solution.
According to experience, Acute and latent viral infections, e.g. laryngitis, bronchitis, sinusitis, pharyn-
to be administered in gitis, inuenzal infections; all diseases caused by mixed infections,
cases of: e.g. Herpes zoster, chicken pox; migraine; multiple sclerosis; vertigo;
Menires disease.
Characteristics: Quentakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Penicillium glabrum).
Adverse reactions: None known.
Interactions
with other remedies: Immunosuppressive drugs can inuence the effectivity of Quentakehl
.
An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: None.
187
Additional advice: Penicillium glabrum as an active ingredient is also contained in
Nota-Quent.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.
188
Quentakehl
5X
Drops
Liquid dilution
for oral intake, rubbing in, inhalation
Active ingredient: Penicillium glabrum e volumine cellulae (lyophil., steril.) 5X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml
Penicillium glabrum e volumine cellulae (lyophil., steril.) 5X
dil. Other constituents: puried water.
According to experience, Acute and latent viral infections, e.g. laryngitis, bronchitis, sinusitis, pharyn-
to be administered in gitis, inuenzal infections; all diseases caused by mixed infections,
cases of: e.g. Herpes zoster, chicken pox; migraine; multiple sclerosis; vertigo;
Menires disease.
Characteristics: Quentakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Penicillium glabrum).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Quentakehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: After opening, contents must be used within two months.
189
Additional advice: Penicillium glabrum as an active ingredient is also contained in
Nota-Quent.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.
190
Rebas
4X
Capsules
for oral intake
Active ingredient: Folliculi lymphatici aggregati (lyophil., steril.) 4X
Composition: 1 capsule contains: Medically active substance: 330 mg Folliculi
lymphatici aggregati (lyophil., steril.) 4X trit. Other constituents:
lactose, hypromellosis (capsule shell).
According to experience, Chronic and recurrent inammations which include disorders of the
to be administered in humoral body defense, gastrointestinal diseases, chronic hepatitis,
cases of: tonsillitis.
Characteristics: Rebas
is produced from Peyers Patches which are a signicant part
of the immune system. It is applied for strengthening humoral immunity
and activating immune support.
Application: Unless otherwise prescribed: 1-3 x daily 1 capsule.
Side effects: Because of specic organic components of Rebas
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,
especially pork protein.
Adverse reactions: None known.
with other remedies:
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 2 ml ampule 10 and 50 5X,
12X, 10 suppositories 4X, 6X, 20 capsules 4X, 6X.
191
Rebas
4X
Suppositories
for rectal application
Active ingredient: Folliculi lymphatici aggregati (lyophil., steril.) 4X
Composition: 1 suppository contains: Medically active substance: 0.2 g Folliculi
lymphatici aggregati (lyophil., steril.) 4X trit. Other constituents:
hard fat, lactose.
According to experience, Chronic and recurrent inammations which include disorders of the
to be administered in humoral body defense, gastrointestinal diseases, chronic hepatitis,
cases of: tonsillitis.
Characteristics: Rebas
is produced from Peyers Patches which are a signicant part
of the immune system. It is applied for strengthening humoral immunity
and activating immune support.
Application: Unless otherwise prescribed: 1 x daily insert 1 suppository rectally.
Side effects: Because of specic organic components of Rebas
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,
especially pork protein.
Adverse reactions: None known.
Interactions None known.
with other remedies:
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 2 ml ampule 10 and 50 5X,
12X, 10 suppositories 4X, 6X, 20 capsules 4X, 6X.
192
Rebas
5X
Ampules
Liquid dilution for injection
Active ingredient: Folliculi lymphatici aggregati (lyophil., steril.) 5X
Composition: 1 ampule of 2 ml contains: Medically active substance: 2 ml Folliculi
lymphatici aggregati (lyophil., steril.) 5X aquous dil. Other
constituents: isotonic sodium chloride solution.
According to experience, Chronic and recurrent inammations which include disorders of the
to be administered in humoral body defense, gastrointestinal diseases, chronic hepatitis,
cases of: tonsillitis.
Characteristics: Rebas
is produced from Peyers Patches which are a signicant part
of the immune system. It is applied for strengthening humoral immunity
and activating immune support.
Application: Unless otherwise prescribed: 1 ampule of 2 ml to be injected either
intramuscularly, subcutaneously or intracutaneously, 1-3 x weekly.
Side effects: Because of specic organic components of Rebas
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,
especially pork protein.
Adverse reactions: None known.
Interactions None known.
with other remedies:
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 2 ml ampule 10 and 50 5X,
12X, 10 suppositories 4X, 6X, 20 capsules 4X, 6X.
193
Rebas
6X
Capsules
for oral intake
Active ingredient: Folliculi lymphatici aggregati (lyophil., steril.) 6X
Composition: 1 capsule contains: Medically active substance: 330 mg Folliculi
lymphatici aggregati (lyophil., steril.) 6X trit. Other constituents:
lactose, hypromellosis (capsule shell).
According to experience, Chronic and recurrent inammations which include disorders of the
to be administered in humoral body defense, gastrointestinal diseases, chronic hepatitis,
cases of: tonsillitis.
Characteristics: Rebas
is produced from Peyers Patches which are a signicant part
of the immune system. It is applied for strengthening humoral immunity
and activating immune support.
Application: Unless otherwise prescribed: 1-3 x daily 1 capsule.
Side effects: Because of specic organic components of Rebas
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,
especially pork protein.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 2 ml ampule 10 and 50 5X,
12X, 10 suppositories 4X, 6X, 20 capsules 4X, 6X.
194
Rebas
6X
Suppositories
for rectal application
Active ingredient: Folliculi lymphatici aggregati (lyophil., steril.) 6X
Composition: 1 suppository contains: Medically active substance: 0.2 g Folliculi
lymphatici aggregati (lyophil., steril.) 6X trit. Other constituents:
hard fat, lactose.
According to experience, Chronic and recurrent inammations which include disorders of the
to be administered in humoral body defense, gastrointestinal diseases, chronic hepatitis,
cases of: tonsillitis.
Characteristics: Rebas
is produced from Peyers Patches which are a signicant part
of the immune system. It is applied for strengthening humoral immunity
and activating immune support.
Application: Unless otherwise prescribed: 1 x daily insert 1 suppository rectally.
Side effects: Because of specic organic components of Rebas
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,
especially pork protein.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This products contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 2 ml ampule 10 and 50 5X,
12X, 10 suppositories 4X, 6X, 20 capsules 4X, 6X.
195
Rebas
12X
Ampules
Liquid dilution for injection
Active ingredient: Folliculi lymphatici aggregati (lyophil., steril.) 12X
Composition: 1 ampule of 2 ml contains: Medically active substance: 2 ml Folliculi
lymphatici aggregati (lyophil., steril.) 12X aquous dil. Other con-
stituents: isotonic sodium chloride solution.
According to experience, Chronic and recurrent inammations which include disorders of the
to be administered in humoral body defense, gastrointestinal diseases, chronic hepatitis,
cases of: tonsillitis.
Characteristics: Rebas
is produced from Peyers Patches which are a signicant part
of the immune system. It is applied for strengthening humoral immunity
and activating immune support.
Application: Unless otherwise prescribed: 1 ampule of 2 ml to be injected either
intramuscularly, subcutaneously or intracutaneously, 1-3 x weekly.
Side effects: Because of specic organic components of Rebas
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,
especially pork protein.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 2 ml ampule 10 and 50 5X,
12X, 10 suppositories 4X, 6X, 20 capsules 4X, 6X.
196
Recarcin
4X
Ampules
Liquid dilution for injection
Active ingredient: Bacillus rmus e volumine cellulae (lyophil., steril.) 4X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1ml Bacillus
rmus e volumine cellulae (lyophil., steril.) 4X aquous dil.. Other
constituents: isotonic sodium chloride solution.
According to experience, All subacute and chronic inammatory diseases, especially of the
to be administered in glands and serosae; arthritis and arthrosis; susceptibility to infection
cases of: (for immune modulation).
Characteristics: Recarcin
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
In cases of known hypersensitivity to Bacillus rmus, as a precaution,
this preparation should not be administered.
Adverse reactions: None known. Generally well tolerated. Occasionally local reactions
like rubefaction, swelling or painfulness may be observed, normally
vanishing without treatment. These effects are not to be seen as
adverse reactions, but rather as an expression of effectiveness. In the
rst 2 or 3 days after the injection sometimes conditions of weakness,
fortied expectoration, slight painfulness of the region or subfebrile
temperatures may show. Strong general reactions are always a sign of
overdose or of incorrect injection technique.
Interactions Immunosuppressive drugs can inuence the effectivity of Recarcin
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
197
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.
198
Recarcin
4X
Capsules
for oral intake
Active ingredient: Bacillus rmus e volumine ex muris cellulae (lyophil., steril.) 4X
Composition: 1 capsule contains: Medically active substance: 330 mg Bacillus
rmus e volumine ex murae cellulae (lyophil., steril.) 4X trit.
Other constituents: lactose, hypromellosis (capsule shell).
According to experience, All subacute and chronic inammatory diseases, especially of the
to be administered in glands and serosae; arthritis and arthrosis; susceptibility to infection
cases of: (for immune modulation).
Characteristics: Recarcin
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
In cases of known hypersensitivity to Bacillus rmus, as a precaution,
this preparation should not be administered.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions Immunosuppressive drugs can inuence the effectivity of Recarcin
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.
199
Recarcin
6X
Ampules
Liquid dilution for injection
Active ingredient: Bacillus rmus e volumine cellulae (lyophil., steril.) 6X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Bacillus
rmus e volumine cellulae (lyophil., steril.) 6X aquous dil. Other
constituents: isotonic sodium chloride solution.
According to experience, All subacute and chronic inammatory diseases, especially of the
to be administered in glands and serosae; arthritis and arthrosis; susceptibility to infection
cases of: (for immune modulation).
Characteristics: Recarcin
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
In cases of known hypersensitivity to Bacillus rmus, as a precaution,
this preparation should not be administered.
Adverse reactions: None known. Generally well tolerated. Occasionally local reactions
like rubefaction, swelling or painfulness may be observed, normally
vanishing without treatment. These effects are not to be seen as
adverse reactions, but rather as an expression of effectiveness. In the
rst 2 or 3 days after the injection sometimes conditions of weakness,
fortied expectoration, slight painfulness of the region or subfebrile
temperatures may show. Strong general reactions are always a sign of
overdose or of incorrect injection technique.
Interactions Immunosuppressive drugs can inuence the effectivity of Recarcin
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
200
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.
201
Recarcin
6X
Capsules
for oral intake
Active ingredient: Bacillus rmus e volumine ex muris cellulae (lyophil., steril.) 6X
Composition: 1 capsule contains: Medically active substance: 330 mg Bacillus rmus
e volumine ex muris cellulae (lyophil., steril.) 6X trit. Other
constituents: lactose, hypromellosis (capsule shell).
According to experience, All subacute and chronic inammatory diseases, especially of the
to be administered in glands and serosae; arthritis and arthrosis; susceptibility to infection
cases of: (for immune modulation).
Characteristics: Recarcin
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
In cases of known hypersensitivity to Bacillus rmus, as a precaution,
this preparation should not be administered.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions Immunosuppressive drugs can inuence the effectivity of Recarcin
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.
202
Recarcin
6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Bacillus rmus e volumine cellulae (lyophil., steril.) 6X
Composition: 5 ml liquid dilution contain: Medically active substance: 5 ml Bacillus
rmus e volumine cellulae (lyophil., steril.) 6X dil. Other con-
stituents: puried water.
According to experience, All subacute and chronic inammatory diseases, especially of the
to be administered in glands and serosae; arthritis and arthrosis; susceptibility to infection
cases of: (for immune modulation).
Characteristics: Recarcin
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
In cases of known hypersensitivity to Bacillus rmus, as a precaution,
this preparation should not be administered.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions Immunosuppressive drugs can inuence the effectivity of Recarcin
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: After opening, contents must be used within two months.
203
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.
204
Recarcin
6X
Suppositories
for rectal application
Active ingredient: Bacillus rmus e volumine ex muris cellulae (lyophil., steril.) 6X
Composition: 1 suppository contains: Medically active substance: 0.2 g Bacillus
rmus e volumine ex muris cellulae cellulae (lyophil., steril.)
6X trit. Other constituents: hard fat, lactose.
According to experience, All subacute and chronic inammatory diseases, especially of the
to be administered in glands and serosae; arthritis and arthrosis; susceptibility to infection
cases of: (for immune modulation).
Characteristics: Recarcin
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
In cases of known hypersensitivity to Bacillus rmus, as a precaution,
this preparation should not be administered.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions Immunosuppressive drugs can inuence the effectivity of Recarcin
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.
205
Relivora
Complex
Ampules
Liquid dilution for injection
Active ingredients: Drosera 3X, Echinacea angustifolia 4X, Juglans 4X
Composition: 1 ampule of 2 ml contains: Medically active substance: 50.0 l Drosera
rotundifolia 3X aquous dil., 500 l Echinacea angustifolia 4X
aquous dil., 500 l Juglans 4X aquous dil. Other constituents: isotonic
sodium chloride solution.
According to experience, Stimulation of the bodys immune system; fever; inammatory processes
to be administered in of the respiratory tract (hard, dry cough), bronchitis, whooping
cases of: cough.
Characteristics: The individual components of Relivora
Complex
Drops
Liquid dilution
for oral intake
Active ingredients: Drosera 3X, Echinacea angustifolia 2X, Juglans 4X
Composition: 10 ml liquid dilution contain: Medically active substance: 0.25 ml
Drosera 3X dil., 0.025 ml Echinacea angustifolia 2X dil., 2.5 ml
Juglans 4X dil. Other constituents: ethanol 22.17 % (m/m), puried
water.
According to experience, Stimulation of the bodys immune system; fever; inammatory processes
to be administered in of the respiratory tract (hard, dry cough), bronchitis, whooping cough.
cases of:
Characteristics: The individual components of Relivora
3X
Suppositories
for rectal application
Active ingredient: Aspergillus ruber e volumine cellulae (lyophil., steril.) 3X
Composition: 1 suppository contains: Medically active substance: 0.2 g Aspergillus
ruber e volumine cellulae (lyophil., steril.) 3X trit. Other
constituents: hard fat, lactose.
According to experience, All chronic diseases of the upper and lower respiratory tract, such as
to be administered in rhinitis, sinusitis, bronchitis, conjunctivitis (red, itching eyes); cystitis
cases of: nephritis.
Characteristics: Observational studies with Ruberkehl
, a homeopathic preparation
from Aspergillus ruber, have shown signicant improvements in all
relevant symptoms of acute allergic rhinitis.
Application: Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Ruberkehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Aspergillus ruber).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Ruberkehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X.
210
Ruberkehl
5X
Ampules
Liquid dilution for injection
Active ingredient: Aspergillus ruber e volumine cellulae (lyophil., steril.) 5X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Aspergillus
ruber e volumine cellulae (lyophil., steril.) 5X aquous dil. Other
constituents: isotonic sodium chloride solution.
According to experience, All chronic diseases of the upper and lower respiratory tract, such as
to be administered in rhinitis, sinusitis, bronchitis, conjunctivitis (red, itching eyes); cystitis,
cases of: nephritis.
Characteristics: Observational studies with Ruberkehl
, a homeopathic preparation
from Aspergillus ruber, have shown signicant improvements in all
relevant symptoms of acute allergic rhinitis.
Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either
intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3x
weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Ruberkehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Aspergillus ruber).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Ruberkehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: None.
211
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X.
212
Ruberkehl
5X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Aspergillus ruber e volumine cellulae (lyophil., steril.) 5X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Asper-
gillus ruber e volumine cellulae (lyophil., steril.) 5X dil. Other
constituents: puried water.
According to experience, All chronic diseases of the upper and lower respiratory tract, such as
to be administered in rhinitis, sinusitis, bronchitis, conjunctivitis (red, itching eyes); cystitis,
cases of: nephritis.
Characteristics: Observational studies with Ruberkehl
, a homeopathic preparation
from Aspergillus ruber, have shown signicant improvements in all
relevant symptoms of acute allergic rhinitis.
Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Ruberkehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Aspergillus ruber).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Ruberkehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: After opening, contents must be used within two months.
213
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X.
214
Sankombi
5X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredients: Mucor racemosus e volumine cellulae (lyophil., steril.) 5X,
Aspergillus niger e volumine cellulae (lyophil., steril.) 5X
Composition: 10 ml liquid dilution contain: Medically active substance: 5 ml Mucor
racemosus e volumine cellulae (lyophil., steril.) 5X dil., 5 ml
Aspergillus niger e volumine cellulae (lyophil., steril.) 5X dil.
Other constituents: puried water.
According to experience, Diseases due to circulatory disorders, such as embolism, thromboses,
to be administered in hemorrhoids; diseases related to a tuberculinic constitution, such as
cases of: degenerative or inammatory conditions (Bechterews disease etc.),
lymphatism.
Characteristics: Sankombi
5X and Nigersan
5X. Mucokehl
is produced
from the mold fungus Mucor racemosus Fresen. It has an inuence
on all disorders of the blood and circulatory system and resulting
diseases. Nigersan
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Mucor racemosus/ Aspergillus niger).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sankombi
with other remedies: 5X. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
215
Advice: After opening, contents must be used within two months.
Additional advice: In isopathic therapy, Sankombi
Acne 5X
Ampules
Liquid dilution for injection
Active ingredient: Propionibacterium acnes extractum (lyophil., steril.) 5X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Propioni-
bacterium acnes extractum (lyophil., steril.) X aqueous dil.
Other constituents: isotonic sodium chloride solution.
According to experience, Acne conglobata; rheumatoid arthritis; venous and cerebral circulatory
to be administered in disorders.
cases of:
Characteristics: Sanukehl
Acne, theo-
retically, hypersensitivity may occur, mainly in the form of skin reactions.
Also allergic reactions against the ingredient Propionibacterium
acnes are possible. In this case, discontinue medication and treat
symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Propioni-
bacterium species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Acne. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: None.
219
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.
220
Sanukehl
Acne 6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Propionibacterium acnes extractum (lyophil., steril.) 6X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml
Propionibacterium acnes extractum (lyophil., steril.) 6X dil.
Other constituents: puried water.
According to experience, Acne conglobata; rheumatoid arthritis; venous and cerebral circulatory
to be administered in disorders.
cases of:
Characteristics: Sanukehl
Acne, theo-
retically, hypersensitivity may occur, mainly in the form of skin reactions.
Also allergic reactions against the ingredient Propionibacterium
acnes are possible. In this case, discontinue medication and treat
symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Propioni-
bacterium species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Acne. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
221
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.
222
Sanukehl
Brucel 6X
Ampules
Liquid dilution for injection
Active ingredient: Brucella melitensis extractum (lyophil., steril.) 6X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Brucella
melitensis extractum (lyophil., steril.) 6X aquous dil. Other
constituents: isotonic sodium chloride solution.
According to experience, Myalgia, subacute polyarthritis; intermittent fever with inuenza symptoms;
to be administered in neurasthenia; orchitis, epididymitis; headaches/migraine; lumbar syn-
cases of: drome.
Characteristics: Sanukehl
Brucel, theo-
retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Brucella
melitensis are possible. In this case, discontinue medication and treat
symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Brucella
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Brucel. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
223
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.
224
Sanukehl
Brucel 6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Brucella melitensis extractum (lyophil., steril.) 6X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Brucella
melitensis extractum (lyophil., steril.) 6X dil. Other constituents:
puried water.
According to experience, Myalgia, subacute polyarthritis; intermittent fever with inuenza symptoms;
to be administered in neurasthenia; orchitis, epididymitis; headaches/migraine; lumbar syn-
cases of: drome.
Characteristics: Sanukehl
Brucel, theo-
retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Brucella
melitensis are possible. In this case, discontinue medication and treat
symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Brucella
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Brucel. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
225
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.
226
Sanukehl
Cand 5X
Ampules
Liquid dilution for injection
Active ingredient: Candida albicans extractum Sero A et B (lyophil., steril.) 5X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Candida
albicans extractum Sero A et B (lyophil., steril.) 5X aquous dil.
Other constituents: isotonic sodium chloride solution.
According to experience, Diseases of the mouth, like stomatitis, gingivitis, perlche, aphthae;
to be administered in intestinal dysbiosis, candida infections, colitis, obstipation after treat-
cases of: ment with antibiotics; allergic asthma; vulvitis, vulvovaginitis, kraurosis
vulvae; dermatosis, e.g. after treatment with antibiotics.
Characteristics: Sanukehl
Cand, theo-
retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Candida
albicans are possible. In this case, discontinue medication and treat
symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Candida
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Cand. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
227
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.
228
Sanukehl
Cand 6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Candida albicans extractum Sero A et B (lyophil., steril.) 6X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Candida
albicans extractum Sero A et B (lyophil., steril.) 6X dil. Other
constituents: puried water.
According to experience, Diseases of the mouth, like stomatitis, gingivitis, perlche, aphthae;
to be administered in intestinal dysbiosis, candida infections, colitis, obstipation after treat-
cases of: ment with antibiotics; allergic asthma; vulvitis, vulvovaginitis, kraurosis
vulvae; dermatosis, e.g. after treatment with antibiotics.
Characteristics: Sanukehl
Cand, theo-
retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Candida
albicans are possible. In this case, discontinue medication and treat
symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Candida
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Cand. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
229
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.
230
Sanukehl
Coli 6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Escherichia coli extractum (lyophil., steril.) 6X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Esche-
richia coli extractum (lyophil., steril.) 6X dil. Other constituents:
puried water.
According to experience, Cholangitis, cholecystitis, gastroenteritis, colitis; pyelonephritis, cystitis;
to be administered in epididymitis, prostatitis; salpingitis, metritis, vaginitis; bronchitis.
cases of:
Characteristics: Sanukehl
Coli, theo-
retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Escherichia
coli are possible. In this case, discontinue medication and treat
symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Escherichia
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Coli. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
231
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 7X.
232
Sanukehl
Coli 7X
Ampules
Liquid dilution for injection
Active ingredient: Escherichia coli extractum (lyophil., steril.) 7X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Escherichia
coli extractum (lyophil., steril.) 7X aquous dil. Other constituents:
isotonic sodium chloride solution.
According to experience, Cholangitis, cholecystitis, gastroenteritis, colitis; pyelonephritis, cystitis;
to be administered in epididymitis, prostatitis; salpingitis, metritis, vaginitis; bronchitis.
cases of:
Characteristics: Sanukehl
Coli, theo-
retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Escherichia
coli are possible. In this case, discontinue medication and treat
symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Escherichia
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Coli. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: None.
233
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 7X.
234
Sanukehl
Klebs 6X
Ampules
Liquid dilution for injection
Active ingredient: Klebsiella pneumoniae extractum (lyophil., steril.) 6X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Klebsiella
pneumoniae extractum (lyophil., steril.) 6X aquous dil. Other
constituents: isotonic sodium chloride solution.
According to experience, Respiratory diseases; dysbiosis after antibiotic therapy.
to be administered in
cases of:
Characteristics: Sanukehl
Klebs, theo-
retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Klebsiella
pneumoniae are possible. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Klebsiella
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Klebs. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: After opening, contents must be used within two months.
235
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.
236
Sanukehl
Klebs 6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Klebsiella pneumoniae extractum (lyophil., steril.) 6X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml
Klebsiella pneumoniae extractum (lyophil., steril.) 6X dil. Other
constituents: puried water.
According to experience, Respiratory diseases; dysbiosis after antibiotic therapy.
to be administered in
cases of:
Characteristics: Sanukehl
Klebs, theo-
retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Klebsiella
pneumoniae are possible. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Klebsiella
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Klebs. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
237
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.
238
Sanukehl
Myc 5X
Ampules
Liquid dilution for injection
Active ingredient: Mycobacterium bovis (BCG) extractum (lyophil., steril.) 5X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Myco-
bacterium bovis (BCG) extractum (lyophil., steril.) 5X aquous
dil. Other constituents: isotonic sodium chloride solution.
According to experience, Respiratory diseases, such as bronchial asthma, pleurisy, rhinitis;
to be administered in chronic recurrent diseases of the skin and the mucous membranes,
cases of: such as juvenile acne, urticaria, hordeolum, psoriasis; lupus erythema-
tosus; arthritis; osteochondrosis; cholecystitis; enterocolitis; ventricular
and duodenal ulcer; headache; metritis; nephritis; otitis.
Characteristics: Sanukehl
Myc, theo-
retically, hypersensitivity may occur, mainly in the form of skin reactions.
Also allergic reactions against the ingredient Mycobacterium bovis
(BCG) are possible. In this case, discontinue medication and treat
symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Mycobacterium
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Myc. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
239
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.
240
Sanukehl
Myc 6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Mycobacterium bovis (BCG) extractum (lyophil., steril.) 6X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml
Mycobacterium bovis (BCG) extractum (lyophil., steril.) 6X dil.
Other constituents: puried water.
According to experience, Respiratory diseases, such as bronchial asthma, pleurisy, rhinitis chronic;
to be administered in recurrent diseases of the skin and the mucous membranes, such as
cases of: juvenile acne, urticaria, hordeolum, psoriasis; lupus erythematosus;
arthritis; osteochondrosis; cholecystitis; enterocolitis; ventricular and
duodenal ulcer; headache; metritis; nephritis; otitis.
Characteristics: Sanukehl
Myc, theo-
retically, hypersensitivity may occur, mainly in the form of skin reactions.
Also allergic reactions against the ingredient Mycobacterium bovis
(BCG) are possible. In this case, discontinue medication and treat
symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Mycobacterium
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Myc. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
241
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.
242
Sanukehl
Prot 6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Proteus vulgaris extractum (lyophil., steril.) 6X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Proteus
vulgaris extractum (lyophil., steril.) 6X dil. Other constituents:
puried water.
According to experience, Otitis; osteomyelitis; intestinal dysbiosis after treatment with antibiotics;
to be administered in ulcerative colitis; angina; rheumatic disorders; chronic suppurative
cases of: affections of the respiratory and intestinal tract.
Characteristics: Sanukehl
Prot, theo-
retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Proteus
vulgaris are possible. In this case, discontinue medication and treat
symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Proteus
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Prot. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: After opening, contents must be used within two months.
243
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 7X.
244
Sanukehl
Prot 7X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Proteus vulgaris extractum (lyophil., steril.) 7X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Proteus
vulgaris extractum (lyophil., steril.) 7X aquous dil. Other
constituents: isotonic sodium chloride solution.
According to experience, Otitis; osteomyelitis; intestinal dysbiosis after treatment with antibiotics;
to be administered in ulcerative colitis; angina; rheumatic disorders; chronic suppurative
cases of: affections of the respiratory and intestinal tract.
Characteristics: Sanukehl
Prot, theo-
retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Proteus
vulgaris are possible. In this case, discontinue medication and treat
symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Proteus species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Prot. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: None.
245
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 7X.
246
Sanukehl
Pseu 6X
Ampules
Liquid dilution for injection
Active ingredient: Pseudomonas aeruginosa extractum (lyophil., steril.) 6X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Pseu-
domonas aeruginosa extractum (lyophil., steril.) 6X aquous dil.
Other constituents: isotonic sodium chloride solution.
According to experience, Respiratory disorders, such as bronchial asthma; otitis; sinusitis; pharyngitis,
to be administered in hay fever, chronic bronchitis; infectious and infectious and allergic
cases of: dermatitis, pruritus, collagenosis, bromyalgia, ulcer cruris, keloids,
burns, autoimmune diseases, treatment of complaints caused by
immunosuppressive treatment.
Characteristics: Sanukehl
Pseu, theo-
retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Pseudomonas
aeruginosa are possible. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Pseudomonas
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Pseu. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
247
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.
248
Sanukehl
Pseu 6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Pseudomonas aeruginosa extractum (lyophil., steril.) 6X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Pseu-
domonas aeruginosa extractum (lyophil., steril.) 6X dil. Other
constituents: puried water.
According to experience, Respiratory disorders, such as bronchial asthma; otitis; sinusitis; pharyn-
to be administered in gitis, hay fever, chronic bronchitis; infectious and infectious and
cases of: allergic dermatitis, pruritus, collagenosis, bromyalgia, ulcer cruris,
keloids, burns, autoimmune diseases, treatment of complaints caused
by immunosuppressive treatment.
Characteristics: Sanukehl
Pseu, theo-
retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Pseudomonas
aeruginosa are possible. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Pseudomonas
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Pseu 6X. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
249
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.
250
Sanukehl
Salm 6X
Ampules
Liquid dilution for injection
Active ingredient: Salmonella enteritidis extractum (lyophil., steril.) 6X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Salmonella
enteritidis extractum (lyophil., steril.) 6X aquous dil. Other
constituents: isotonic sodium chloride solution.
According to experience, Impaired development; chronic pancreatitis, chronic gastroenteritis;
to be administered in celiac disease; rheumatic fever.
cases of:
Characteristics: Sanukehl
Salm, theo-
retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Salmonella
enteritidis are possible. In this case, discontinue medication and treat
symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Salmonella
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Salm. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: None.
251
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.
252
Sanukehl
Salm 6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Salmonella enteritidis extractum (lyophil., steril.) 6X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml
Salmonella enteritidis extractum (lyophil., steril.) 6X dil. Other
constituents: puried water.
According to experience, Impaired development; chronic pancreatitis, chronic gastroenteritis;
to be administered in celiac disease; rheumatic fever.
cases of:
Characteristics: Sanukehl
Salm, theo-
retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Salmonella
enteritidis are possible. In this case, discontinue medication and treat
symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Salmonella
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Salm. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
253
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.
254
Sanukehl
Serra 6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Serratia marcescens extractum (lyophil., steril.) 6X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml
Serratia marcescens extractum (lyophil., steril.) 6X dil. Other
constituents: puried water.
According to experience, Nosocomial infections with Serratia marcescens.
to be administered in
cases of:
Characteristics: Sanukehl
Serra, theo-
retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Serratia
marcescens are possible. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Serratia
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Serra. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
255
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 7X.
256
Sanukehl
Serra 7X
Ampules
Liquid dilution for injection
Active ingredient: Serratia marcescens extractum (lyophil., steril.) 7X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Serratia
marcescens extractum (lyophil., steril.) 7X aquous dil. Other
constituents: isotonic sodium chloride solution.
According to experience, Nosocomial infections with Serratia marcescens.
to be administered in
cases of:
Characteristics: Sanukehl
Serra,
theoretically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Serratia
marcescens are possible. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Serratia
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Serra. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: None.
257
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 7X.
258
Sanukehl
Staph 5X
Ampules
Liquid dilution for injection
Active ingredient: Staphylococcus aureus extractum (lyophil., steril.) 5X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Staphy-
lococcus aureus extractum (lyophil., steril.) 5X aquous dil. Other
constituents: isotonic sodium chloride solution.
According to experience, Folliculosis, furunculosis, impetigo, acne conglobata; blepharitis, hor-
to be administered in deolum, chalazion, angina, otitis, mastoiditis, sinusitis; meningitis;
cases of: osteomyelitis; nephritis, urogenital infections with staphylococci.
Characteristics: Sanukehl
Staph, theo-
retically, hypersensitivity may occur, mainly in the form of skin reactions.
Also allergic reactions against the ingredient Staphylococcus
aureus are possible. In this case, discontinue medication and treat
symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Staphylococcus
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Staph. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
259
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.
260
Sanukehl
Staph 6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Staphylococcus aureus extractum (lyophil., steril.) 6X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml
Staphylococcus aureus extractum (lyophil., steril.) 6X dil.
Other constituents: puried water.
According to experience, Folliculosis, furunculosis, impetigo, acne conglobata; blepharitis,
to be administered in hordeolum, chalazion, angina, otitis, mastoiditis, sinusitis; meningitis;
cases of: osteomyelitis; nephritis, urogenital infections with staphylococci.
Characteristics: Sanukehl
Staph, theo-
retically, hypersensitivity may occur, mainly in the form of skin reactions.
Also allergic reactions against the ingredient Staphylococcus
aureus are possible. In this case, discontinue medication and treat
symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Staphylococcus
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Staph. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: After opening, contents must be used within two months.
261
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.
262
Sanukehl
Strep 5X
Ampules
Liquid dilution for injection
Active ingredient: Streptococcus pyogenes extractum (lyophil., steril.) 5X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Strepto-
coccus pyogenes extractum (lyophil., steril.) 5X aquous dil.
Other constituents: isotonic sodium chloride solution.
According to experience, Angina tonsillaris; eczema; endo-, myo- and pericarditis; empyema;
to be administered in mastitis puerperalis; osteomyelitis; otitis media; sinubronchitis; phleg-
cases of: mons; primary chronic polyarthritis.
Characteristics: Sanukehl
Strep, theo-
retically, hypersensitivity may occur, mainly in the form of skin reactions.
Also allergic reactions against the ingredient Streptococcus
pyogenes are possible. In this case, discontinue medication and treat
symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Streptococcus
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Strep. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: None.
263
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.
264
Sanukehl
Strep 6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Streptococcus pyogenes extractum (lyophil., steril.) 6X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Strep-
tococcus pyogenes extractum (lyophil., steril.) 6X dil. Other
constituents: puried water.
According to experience, Angina tonsillaris; eczema; endo-, myo- and pericarditis; empyema;
to be administered in mastitis puerperalis; osteomyelitis; otitis media; sinubronchitis; phleg-
cases of: mons; primary chronic polyarthritis.
Characteristics: Sanukehl
Strep, theo-
retically, hypersensitivity may occur, mainly in the form of skin reactions.
Also allergic reactions against the ingredient Streptococcus
pyogenes are possible. In this case, discontinue medication and treat
symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Streptococcus
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Strep. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
265
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.
266
Sanukehl
Trich 5X
Ampules
Liquid dilution for injection
Active ingredient: Trichophyton verrucosum extractum (lyophil., steril.) 5X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Tricho-
phyton verrucosum extractum (lyophil., steril.) 5X aquous dil.
Other constituents: isotonic sodium chloride solution.
According to experience, Mycosis of the hair, skin, nails, tinea, trichophytosis; impairment of skin
to be administered in function; hair loss.
cases of:
Characteristics: Sanukehl
Trich, theo-
retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Trichophyton
verrucosum are possible. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Trichophyton
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Trich. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: None.
267
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.
268
Sanukehl
Trich 6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Trichophyton verrucosum extractum (lyophil., steril.) 6X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml
Trichophyton verrucosum extractum (lyophil., steril.) 6X dil.
Other constituents: puried water.
According to experience, Mycosis of the hair, skin, nails, tinea, trichophytosis; impairment of
to be administered in skin function; hair loss.
cases of:
Characteristics: Sanukehl
Trich, theo-
retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Trichophyton
verrucosum are possible. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Trichophyton
species.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Sanukehl
with other remedies: Trich. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
269
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.
270
Sanumgerman
6X
Drops
Liquid dilution for oral intake
Active ingredient: Di-potassium-germanium(IV)-citrate-L(+)lactate 6X
Composition: 100 ml liquid dilution contain: Medically active substance: 100 ml
Di-potassium-germanium(IV)-citrate-L(+)lactate 6X dil. Other
constituents: puried water, ethanol.
According to experience, Peripheral arterial circulatory disorders, cerebrosclerosis, Raynauds
to be administered in disease; chronic rheumatism; Parkinsons disease; epilepsy; adjuvant
cases of: therapy for cancer.
Characteristics: Sanumgerman
1X
Ointment
for rubbing in
Active ingredient: Acidum lacticum 1X
Composition: 1 g ointment contains: Medically active substance: 0.1 g Acidum
lacticum 1X dil. Other constituents: 0.38 g lanolin alcohol ointment,
0.10 g coconut oil fract., 0.03 g glyceryl monostearate 40-55%, 0.23
g propylene glycol, 0.02 g magnesium sulphate x 7 H2O, 0.01 g lactic
acid, 0.14 g water for injection.
According to experience, Regulation of the pH value, especially for chronic skin diseases like
to be administered in psoriasis, ichthyosis, rhagades.
cases of:
Characteristics: Sanuvis
2X
Drops
Liquid dilution for oral intake
Active ingredient: Acidum lacticum 2X
Composition: 1 ml liquid dilution contains: Medically active substance: 1 ml Acidum
lacticum 2X dil. Other constituents: puried water, ethanol.
According to experience, Disorders of the acid alkaline balance, metabolic disturbances mainly
to be administered in resulting from the increased production of levorotatory lactic acid e.g.
cases of: diabetes, tissue degeneration and functional heart disorders; skin
diseases such as psoriasis and ichthyosis.
Characteristics: Sanuvis
Ampules
Liquid dilution for injection
Active ingredient: Acidum lacticum 4X/6X/12X/30X/200X
Composition: 1 ampule of 2 ml contains: Medically active substance: 0.4 ml Acidum
lacticum 4X aquous dil., 0.4 ml Acidum lacticum 6X aquous dil.,
0.4 ml Acidum lacticum 12X aquous dil., 0.4 ml Acidum lacticum
30X aquous dil., 0.4 ml Acidum lacticum 200X aquous dil. Other
constituents: isotonic sodium chloride solution.
According to experience, Disorders of the acid alkaline balance and of intermediary metabolism;
to be administered in chronic skin diseases and circulatory disorders.
cases of:
Characteristics: Sanuvis
can be administered
as a basic remedy in addition to the fungal preparations. In Isopathy,
Sanuvis
.
Application: Unless otherwise prescribed: 1 ampule of 2 ml to be injected intramus-
cularly, 1-3 x weekly.
Side effects: None known.
Contraindications: None known.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 30 ml dropper bottle 2X, 100
ml dropper bottle 4X/6X/12X/30X/200X potency mixture, 2 ml ampule
10 and 50 4X/6X/12X/30X/200X potency mixture, 80 tablets 4X/6X/12X/
30X/200X potency mixture, 30 g tube of ointment 1X.
275
Sanuvis
Drops
Liquid dilution for oral intake
Active ingredient: Acidum lacticum 4X/6X/12X/30X/200X
Composition: 100 ml liquid dilution contains: Medically active substance: 20 ml
Acidum lacticum 4X dil., 20 ml Acidum lacticum 6X dil., 20 ml
Acidum lacticum 12X dil., 20 ml Acidum lacticum 30X dil., 20
ml Acidum lacticum 200X dil. Other constituents: puried water,
ethanol.
According to experience, Disorders of the acid alkaline balance and of intermediary metabolism;
to be administered in chronic skin diseases and circulatory disorders.
cases of:
Characteristics: Sanuvis
can be administered
as a basic remedy in addition to the fungal preparations. In Isopathy,
Sanuvis
.
Application: Unless otherwise prescribed: For oral intake: 1-3 x daily 5-20 drops.
Side effects: None known.
Contraindications: This product contains 36.2 % (v/v) alcohol (ethanol). This may present
a health risk in cases of liver diseases, alcoholism, epilepsy, brain
damage, pregnancy, and in children. The action of other drugs may be
reduced or intensied.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains 36.2 % (v/v) alcohol (ethanol).
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 30 ml dropper bottle 2X, 100
ml dropper bottle 4X/6X/12X/30X/200X potency mixture, 2 ml ampule
10 and 50 4X/6X/12X/30X/200X potency mixture, 80 tablets 4X/6X/12X/
30X/200X potency mixture, 30 g tube of ointment 1X.
276
Sanuvis
Tablets
for oral intake
Active ingredient: Acidum lacticum 4X/6X/12X/30X/200X
Composition: 1 tablet contains: Medically active substance: 50 mg Acidum lacticum
4X trit., 50 mg Acidum lacticum 6X trit., 50 mg Acidum lacticum
12X trit., 50 mg Acidum lacticum 30X trit., 50 mg Acidum lacticum
200X trit. Other constituents: lactose, potato starch, magnesium
stearate.
According to experience, Disorders of the acid alkaline balance and of intermediary metabolism;
to be administered in chronic skin diseases and circulatory disorders.
cases of:
Characteristics: Sanuvis
can be administered
as a basic remedy in addition to the fungal preparations. In Isopathy,
Sanuvis
.
Application: Unless otherwise prescribed: 1-3 x daily 1-2 tablets.
Side effects: None known.
Contraindications: None known.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 30 ml dropper bottle 2X, 100
ml dropper bottle 4X/6X/12X/30X/200X potency mixture, 2 ml ampule
10 and 50 4X/6X/12X/30X/200X potency mixture, 80 tablets 4X/6X/12X/
30X/200X potency mixture, 30 g tube of ointment 1X.
277
Selenokehl
4X
Ampules
Liquid dilution for injection
Active ingredient: Natrium selenosum 4X
Composition: 1 ampule of 2 ml contains: Medically active substance: 0.16 ml
Natrium selenosum 4X aquous dil. Other constituents: isotonic
sodium chloride solution.
According to experience, Selenium deciency due to malnutrition and malabsorption, for amal-
to be administered in gam detoxication.
cases of:
Characteristics: Selenium is an essential trace element. In the human body it is chiey
connected with the enzyme glutathione peroxidase which is a constituent
of the antioxidative protective system of the cell. In test models it has
been proven that the selenium-containing glutathione peroxidase is one
of the bodys strongest, most effective enzymes for absorbing radicals.
Among other benets, it lowers the rate of peroxidation of lipids and
thereby protects the cellular membrane from damages. Selenium
deciency increases the toxicity of heavy metals such as mercury, lead
and cadmium, and also it potentizes weakness of the liver caused by
oxidative and chemical inuences.
Application: Unless otherwise prescribed: 1 ampule of 2 ml to be injected either
intramuscularly, subcutaneously, intracutaneously or intravenously, 1-2
x daily.
Side effects: None known.
Contraindications: None known.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: None.
278
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml and 30 ml dropper
bottle 4X, 2 ml ampule 10 and 50 4X.
279
Selenokehl
4X
Drops
Liquid dilution for oral intake
Active ingredient: Natrium selenosum 4X
Composition: 10 ml liquid dilution contain: Medically active substance: 0.8 ml Natrium
selenosum 4X dil. Other constituents: puried water, ethanol 15 %
(m/m).
According to experience, Selenium deciency due to malnutrition and malabsorption, for amal-
to be administered in gam detoxication.
cases of:
Characteristics: Selenium is an essential trace element. In the human body it is chiey
connected with the enzyme glutathione peroxidase which is a constituent
of the antioxidative protective system of the cell. In test models it has
been proven that the selenium-containing glutathione peroxidase is one
of the bodys strongest, most effective enzymes for absorbing radicals.
Among other benets, it lowers the rate of peroxidation of lipids and
thereby protects the cellular membrane from damages. Selenium
deciency increases the toxicity of heavy metals such as mercury, lead
and cadmium, and also it potentizes weakness of the liver caused by
oxidative and chemical inuences.
Application: Unless otherwise prescribed: For oral intake: in case of acute conditions
every half to one hour not more than 6 times daily each 5 drops. In case
of chronic conditions 1-3 x daily 5 drops.
Side effects: None known.
Contraindications: None known.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains 20 % (v/v) alcohol (ethanol).
Due to the alcohol content, professional medical advice should be
sought prior to recommending this product to patients with alcohol or
liver problems.
280
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml and 30 ml dropper
bottle 4X, 2 ml ampule 10 and 50 4X.
281
Silvaysan
Capsules
for oral intake
Active ingredient: Milk-thistle dry extract, rened and standardised
Composition: 1 Capsule contains: 136 - 160 mg Milk-thistle dry extract, rened
and standardised (50-70:1) equivalent to 86,6 mg Silymarin, taken into
account for Silibinin (extractive substance: acetone). Standardisation
material: dextrose 0 to 24 mg. Other constituents: highly dispersed
silica, dextrose, lactose 1 H2O, magnesium stearate, gelatin, puried
water.
Indication: Supporting treatment of chronic inammatory liver diseases and cirrhosis
of the liver as well as toxic liver damage.
This remedy is not intended for treatment of acute poisoning.
Characteristics: Silymarins therapeutic effects are based on two targets or modes of
action: Silymarin changes the structure of the outer cell membrane of
the hepatocytes in such a way that hepatotoxins cannot enter into the
cell. Silymarin stimulates the activity of the nucleolar polymerase A,
resulting in an increased ribosomal protein synthesis, thus stimulating
the regenerative power of the liver and the neogenesis of hepatocytes.
Application: Unless otherwise prescribed: 3 x daily 1 capsule.
Side effects: Occasionally, gastrointestinal complaints, such as nausea or a mild
laxative effect. In rare cases hypersensitivity reactions such as rash,
itching, breathing difculties may occur. In this case, discontinue
medication and treat symptomatically.
Contraindications: This preparation should not be administered if cases of hypersensitivity
against milk-thistle and/or other compositae as well as any of the
ingredients are known.
Adverse reactions: None known.
Interactions The improvement of liver function under intake of Silvaysan
inuences
with other remedies: the metabolism of other concurrently taken drugs. Possibly, dosage
adjustments become necessary.
Simultaneous intake of Silvaysan
and Amiodaron (drug for treatment
of cardiac arrhythmia) may lead to an increased antiarrhythmic effect of
Amiodaron.
282
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: The drug therapy does not replace the avoidance of the hepatotoxic
causes (e.g. alcohol). In case of icterus (light- to dark-yellow colored
skin, yellow colored sclera), professional medical advice should be
sought immediately. Silvaysan
is not suitable for the treatment of
acute intoxication.
This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 20 and 100 capsules.
283
Stolonikehl 6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Penicillium brevicompactum e volumine cellulae (lyophil., steril.) 6X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml
Penicillium brevicompactum e volumine cellulae (lyophil.,
steril.) 6X dil. Other constituents: puried water.
According to experience, Intercostal neuralgia; trigeminal neuralgia.
to be administered in
cases of:
Characteristics: Penicillium stoloniferum, an ubiquitous mold fungus, has proven its
worth for treatment of viral diseases.
Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Stolonikehl, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
(Penicillium brevicompactum).
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Stolonikehl.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage form is available: 10 ml dropper bottle 6X.
284
Strophantus 4X Sanum
Drops
Liquid dilution
for oral intake
Active ingredient: Strophantus gratus 4X dil.
Composition: 1 ml liquid dilution contains: Medically active substance: 1 ml
Strophanthus gratus 4X dil. Other constituents: puried water,
ethanol.
Indication: Cardiac weakness, increasing blood volume, hypertension; sodium
burden; nervous heart by reason of smoking; arteriosclerosis; cardiac
decompensation; anticipatory anxiety.
Characteristics: Strophanthin, also known as Ouabain, was used by the African
natives as arrow poison for a long time. It is produced from a milk-
secreting climbing plant, but it is also an endogenous hormone which
is produced in the adrenal gland and is involved in the regulation of salt
and water balance. The human hypophysis contains an isomer of g-
Strophanthin. Therefore, g-Strophanthin is an endogenic substance. By
its inuence, myocardial activity can be relieved signicantly. Weakness
of the adrenal gland which often occurs with increasing age, as well as
senile heart weakness can be balanced with G-Strophanthin.
Application: Unless otherwise prescribed:
For oral intake: in case of acute conditions 5 drops every half to full
hour up to a maximum of 12 times daily. In case of chronic conditions 5
drops up to 3 times daily.
Side effects: Because of the specic organic components of Strophantus 4X
Sanum, theoretically, hypersensitivity may occur. In this case,
discontinue use and treat symptomatically.
Contraindications: This product contains 51 % (v/v) alcohol (ethanol). Following the dosage
recommendations for acute conditions the alcohol intake amounts up
to 0.3g; following the dosage recommendations for chronic conditions
the alcohol intake amounts up to 0.15g. This may present a health
risk in cases of liver diseases, alcoholism, epilepsy, brain damage,
pregnancy, and in children. The action of other drugs may be reduced
or intensied.
Adverse reactions: None known.
Interactions
with other remedies: None known.
285
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children. This also applies to patients with renal insufciency and
patients with heart failure.
Strophantus 4X Sanum should not be administered with other
preparations containing cardiac glycosides.
Advice: This product contains 51 % (v/v) alcohol (ethanol). Following the dosage
recommendations for acute conditions the alcohol intake amounts up
to 0.3g; following the dosage recommendations for chronic conditions
the alcohol intake amounts up to 0.15g. This may present a health
risk in cases of liver diseases, alcoholism, epilepsy, brain damage,
pregnancy, and in children. The action of other drugs may be reduced
or intensied.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml, 30ml, 100 ml dropper
bottle 4X, 80 tablets 4X.
286
Strophantus 4X Sanum
Tablets
for oral intake
Active ingredient: Strophantus gratus 4X
Composition: 1 tablet contains: Medically active substance: 250 mg Strophanthus
gratus 4X trit. Other constituents: lactose, potato starch, magnesium
stearate.
Indication: Cardiac weakness, increasing blood volume, hypertension; sodium
burden; nervous heart by reason of smoking; arteriosclerosis; cardiac
decompensation; anticipatory anxiety.
Characteristics: Strophanthin, also known as Ouabain, was used by the African
natives as arrow poison for a long time. It is produced from a milk-
secreting climbing plant, but it is also an endogenous hormone which
is produced in the adrenal gland and is involved in the regulation of salt
and water balance. The human hypophysis contains an isomer of g-
Strophanthin. Therefore, g-Strophanthin is an endogenic substance. By
its inuence, myocardial activity can be relieved signicantly. Weakness
of the adrenal gland which often occurs with increasing age, as well as
senile heart weakness can be balanced with G-Strophanthin.
Application: Unless otherwise prescribed:
For oral intake: in case of acute conditions 1 tablet every half to full
hour up to a maximum of 12 times daily. In case of chronic conditions 2
tablets daily.
Side effects: Because of the specic organic components of Strophantus 4X
Sanum, theoretically, hypersensitivity may occur. In this case,
discontinue use and treat symptomatically.
Contraindications: None known.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children. This also applies to patients with renal insufciency and
patients with heart failure.
Strophantus 4X Sanum should not be administered with other
preparations containing cardiac glycosides.
287
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml, 30ml, 100 ml dropper
bottle 4X, 80 tablets 4X.
288
Taraxan
3X
Ampules
Liquid dilution for injection
Active ingredient: Taraxacum ofcinale 3X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml
Taraxacum ofcinale 3X aquous dil. Other constituents: isotonic
sodium chloride solution.
According to experience, Blood and tissue cleansing; stimulation of digestive juices, especially
to be administered in bile ow; kidney support.
cases of:
Characteristics: Taraxacum ofcinale is rich in tannins and bitter substances,
especially taraxin, as well as inulin, fructose, minerals and trace
elements. Since the Middle Ages, various dandelion preparations were
used as food and as plant drugs for liver and kidney support, thus
enabling blood and tissue cleansing.
The following symptoms result from the homeopathic drug picture of
Taraxacum ofcinale: main effects on liver, bile and urine excretion;
strained muscles and joints of the entire body; venous congestions;
upper abdominal complaints; pruritus. Motion improves the symptoms;
resting, lying down and cold, wet weather worsen the complaints.
Taraxan
1X
Drops
Liquid dilution
for oral intake
Active ingredient: Usnea barbata e thallo siccato mother tincture
Composition: 1 ml liquid dilution contain: Medically active substance: 1 ml Usnea
barbata e thallo siccato 1X dil. Other constituents: puried water,
ethanol 62 % (m/m).
According to experience, Congestive headaches; sunstroke; gall bladder disorders; elimination
to be administered in of heavy metals.
cases of:
Characteristics: Usneabasan
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: This product contains 70 % (v/v) alcohol (ethanol). This may present
a health risk in cases of liver diseases, alcoholism, epilepsy, brain
damage, pregnancy, and in children. The action of other drugs may be
reduced or intensied.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
297
Advice: This product contains 70 % (v/v) alcohol (ethanol).
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage form is available: 30 ml dropper bottle 1X.
298
Ustilakehl
5X
Ampules
Liquid dilution for injection
Active ingredient: Ustilago zeae e volumine cellulae (lyophil., steril.) 5X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Ustilago
zeae e volumine cellulae (lyophil., steril.) 5X aquous dil. Other
constituents: isotonic sodium chloride solution.
According to experience, Uterine haemorrhage, membranous dysmenorrhoea, menopausal syn-
to be administered in drome, menorrhagia, metrorrhagia; headache caused by menstruation,
cases of: migraine.
Characteristics: Ustilago zeae, the corn-smut, is a parasitary fungus that attacks all
parts of the maize plant and forms bump-like distensions lled with
spore powder. As the maize plant itself, the rst medicinal use of the
drug came from America. It was predominantly used in folk medicine by
the Afro-American population. The ergotamine-like action of the corn-
smut in the uterus determines its main effect.
Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected subcuta-
neously, 1-3 x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Ustilakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Ustilago zeae.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Ustilakehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: None.
299
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 5X.
300
Ustilakehl
5X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Ustilago zeae e volumine cellulae (lyophil., steril.) 5X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml
Ustilago zeae e volumine cellulae (lyophil., steril.) 5X dil. Other
constituents: puried water.
According to experience, Uterine haemorrhage, membranous dysmenorrhoea, menopausal syn-
to be administered in drome, menorrhagia, metrorrhagia; headache caused by menstruation,
cases of: migraine.
Characteristics: Ustilago zeae, the corn-smut, is a parasitary fungus that attacks all
parts of the maize plant and forms bump-like distensions lled with
spore powder. As the maize plant itself, the rst medicinal use of the
drug came from America. It was predominantly used in folk medicine by
the Afro-American population. The ergotamine-like action of the corn-
smut in the uterus determines its main effect.
Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Ustilakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Ustilago
zeae.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Ustilakehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
301
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 5X.
302
Ustilakehl
5X
Suppositories
for rectal application
Active ingredient: Ustilago zeae e volumine cellulae (lyophil., steril.) 5X
Composition: 1 suppository contains: Medically active substance: 0.2 g Ustilago
zeaee volumine cellulae (lyophil., steril.) 5X trit. Other consti-
tuents: hard fat, lactose.
According to experience, Uterine haemorrhage, membranous dysmenorrhoea, menopausal syn-
to be administered in drome, menorrhagia, metrorrhagia; headache caused by menstruation,
cases of: migraine.
Characteristics: Ustilago zeae, the corn-smut, is a parasitary fungus that attacks all
parts of the maize plant and forms bump-like distensions lled with
spore powder. As the maize plant itself, the rst medicinal use of the
drug came from America. It was predominantly used in folk medicine by
the Afro-American population. The ergotamine-like action of the corn-
smut in the uterus determines its main effect.
Application: Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.
Side effects: Because of specic organic components of Ustilakehl
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to Ustilago
zeae.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Ustilakehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
303
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 5X.
304
Utilin
4X
Ampules
Liquid dilution for injection
Active ingredient: Bacillus subtilis e volumine cellulae (lyophil., steril.) 4X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Bacillus
subtilis e volumine cellulae (lyophil., steril.) 4X aquous dil..
Other constituents: isotonic sodium chloride solution.
According to experience, All subacute and chronic inammatory diseases; intestinal dysfunction,
to be administered in liver and gallbladder disorders; for immune modulation; Basedows
cases of: disease; postmenopause disorders.
Characteristics: Utilin
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
Do not administer in cases of known hypersensitivity to Bacillus
subtilis.
Adverse reactions: None known. Generally well tolerated. Occasionally local reactions
like rubefaction, swelling or painfulness may be observed, normally
vanishing without treatment. These effects are not to be seen as
adverse reactions, but rather as an expression of effectiveness. In the
rst 2 or 3 days after the injection sometimes conditions of weakness,
fortied expectoration, slight painfulness of the region or subfebrile
temperatures may show. Strong general reactions are always a sign of
overdose or of incorrect injection technique.
Interactions Immunosuppressive drugs can inuence the effectivity of Utilin
. An
with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
305
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.
306
Utilin
4X
Capsules
for oral intake
Active ingredient: Bacillus subtilis e volumine ex muris cellulae (lyophil., steril.)
4X
Composition: 1 capsule contains: Medically active substance: 330 mg Bacillus
subtilis e volumine ex muris cellulae (lyophil., steril.) 4X trit.
Other constituents: lactose, hypromellosis (capsule shell).
According to experience, All subacute and chronic inammatory diseases; intestinal dysfunction,
to be administered in liver and gallbladder disorders; for immune modulation; Basedows
cases of: disease; postmenopause disorders.
Characteristics: Utilin
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
Do not administer in cases of known hypersensitivity to Bacillus
subtilis.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions Immunosuppressive drugs can inuence the effectivity of Utilin
. An
with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
307
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.
308
Utilin
6X
Ampules
Liquid dilution for injection
Active ingredient: Bacillus subtilis e volumine cellulae (lyophil., steril.) 6X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Bacillus
subtilis e volumine cellulae (lyophil., steril.) 6X aquous dil..
Other constituents: isotonic sodium chloride solution.
According to experience, All subacute and chronic inammatory diseases; intestinal dysfunction,
to be administered in liver and gallbladder disorders; for immune modulation; Basedows
cases of: disease; postmenopause disorders.
Characteristics: Utilin
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
Do not administer in cases of known hypersensitivity to Bacillus
subtilis.
Adverse reactions: Generally well tolerated. Occasionally local reactions like rubefaction,
swelling or painfulness may be observed, normally vanishing without
treatment. These effects are not to be seen as adverse reactions, but
rather as an expression of effectiveness. In the rst 2 or 3 days after the
injection sometimes conditions of weakness, fortied expectoration,
slight painfulness of the region or subfebrile temperatures may show.
Strong general reactions are always a sign of overdose or of incorrect
injection technique.
Interactions Immunosuppressive drugs can inuence the effectivity of Utilin
. An
with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
309
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.
310
Utilin
6X
Capsules
for oral intake
Active ingredient: Bacillus subtilis e volumine ex muris cellulae (lyophil., steril.)
6X
Composition: 1 capsule contains: Medically active substance: 330 mg Bacillus
subtilis e volumine ex muris cellulae (lyophil., steril.) 6X trit.
Other constituents: lactose, hypromellosis (capsule shell).
According to experience, All subacute and chronic inammatory diseases; intestinal dysfunction,
to be administered in liver and gallbladder disorders; for immune modulation; Basedows
cases of: disease; postmenopause disorders.
Characteristics: Utilin
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
Do not administer in cases of known hypersensitivity to Bacillus
subtilis.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions Immunosuppressive drugs can inuence the effectivity of Utilin
. An
with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
311
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.
312
Utilin
6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Bacillus subtilis e volumine cellulae (lyophil., steril.) 6X
Composition: 5 ml liquid dilution contain: Medically active substance: 5 ml Bacillus
subtilis e volumine cellulae (lyophil., steril.) 6X dil. Other
constituents: puried water.
According to experience, All subacute and chronic inammatory diseases; intestinal dysfunction,
to be administered in liver and gallbladder disorders; for immune modulation; Basedows
cases of: disease; postmenopause disorders.
Characteristics: Utilin
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
Do not administer in cases of known hypersensitivity to Bacillus
subtilis.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions Immunosuppressive drugs can inuence the effectivity of Utilin
. An
with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
313
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.
314
Utilin
6X
Suppositories
for rectal application
Active ingredient: Bacillus subtilis e volumine ex muris cellulae (lyophil., steril.)
6X
Composition: 1 suppository contains: Medically active substance: 0.2 g Bacillus
subtilis e volumine ex muris cellulae (lyophil., steril.) 6X trit.
Other constituents: hard fat, lactose.
According to experience, All sub-acute and chronic inammatory diseases, intestinal dysfunction,
to be administered in liver and gallbladder disorders, for immune modulation, Basedows
cases of: disease, postmenopause disorders.
Characteristics: Utilin
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
Do not administer in cases of known hypersensitivity to Bacillus
subtilis.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions Immunosuppressive drugs can inuence the effectivity of Utilin
. An
with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.
Advice: This product contains lactose.
315
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.
316
Utilin S
4X
Ampules
Liquid dilution for injection
Active ingredient: Mycobacterium phlei e volumine cellulae (lyophil., steril.) 4X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Myco-
bacterium phlei e volumine cellulae (lyophil., steril.) 4X
aquous dil. Other constituents: isotonic sodium chloride solution.
According to experience, All chronic lung diseases; chronic feverish diseases with night sweats
to be administered in and debility, subfebrile temperatures, weakness (for immune modu-
cases of: lation).
Characteristics: Utilin S
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
In cases of known hypersensitivity to Mycobacterium phlei, as a
precaution, this preparation should not be administered.
Adverse reactions: Generally well tolerated. Occasionally local reactions like rubefaction,
swelling or painfulness may be observed, normally vanishing without
treatment. These effects are not to be seen as adverse reactions, but
rather as an expression of effectiveness. In the rst 2 or 3 days after the
injection sometimes conditions of weakness, fortied expectoration,
slight painfulness of the region or subfebrile temperatures may show.
Strong general reactions are always a sign of overdose or of incorrect
injection technique.
Interactions Immunosuppressive drugs can inuence the effectivity of Utilin S
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
317
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.
318
Utilin S
4X
Capsules
for oral intake
Active ingredient: Mycobacterium phlei e volumine ex muris cellulae (lyophil.,
steril.) 4X
Composition: 1 capsule contains: Medically active substance: 330 mg Bacillus
subtilis e volumine ex muris cellulae (lyophil., steril.) 4X trit.
Other constituents: lactose, hypromellosis (capsule shell).
According to experience, All chronic lung diseases; chronic feverish diseases with night sweats
to be administered in and debility, subfebrile temperatures, weakness (for immune modu-
cases of: lation).
Characteristics: Utilin S
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
In cases of known hypersensitivity to Mycobacterium phlei, as a
precaution, this preparation should not be administered.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions Immunosuppressive drugs can inuence the effectivity of Utilin S.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
319
Advice: This product contains lactose.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.
320
Utilin S
6X
Ampules
Liquid dilution for injection
Active ingredient: Mycobacterium phlei e volumine cellulae (lyophil., steril.) 6X
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Myco-
bacterium phlei e volumine cellulae (lyophil., steril.) 6X
aquous dil. Other constituents: isotonic sodium chloride solution.
According to experience, All chronic lung diseases; chronic feverish diseases with night sweats
to be administered in and debility, subfebrile temperatures, weakness (for immune modu-
cases of: lation).
Characteristics: Utilin S
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
In cases of known hypersensitivity to Mycobacterium phlei, as a
precaution, this preparation should not be administered.
Adverse reactions: Generally well tolerated. Occasionally local reactions like rubefaction,
swelling or painfulness may be observed, normally vanishing without
treatment. These effects are not to be seen as adverse reactions, but
rather as an expression of effectiveness. In the rst 2 or 3 days after the
injection sometimes conditions of weakness, fortied expectoration,
slight painfulness of the region or subfebrile temperatures may show.
Strong general reactions are always a sign of overdose or of incorrect
injection technique.
Interactions Immunosuppressive drugs can inuence the effectivity of Utilin S
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
321
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.
322
Utilin S
6X
Capsules
for oral intake
Active ingredient: Mycobacterium phlei e volumine ex muris cellulae (lyophil.,
steril.) 6X
Composition: 1 capsule contains: Medically active substance: 330 mg Bacillus
subtilis e volumine ex muris cellulae (lyophil., steril.) 6X trit.
Other constituents: lactose, hypromellosis (capsule shell).
According to experience, All chronic lung diseases; chronic feverish diseases with night sweats
to be administered in and debility, subfebrile temperatures, weakness (for immune modu-
cases of: lation).
Characteristics: Utilin S
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
In cases of known hypersensitivity to Mycobacterium phlei, as a
precaution, this preparation should not be administered.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions Immunosuppressive drugs can inuence the effectivity of Utilin S
.
with other remedies: An interval of 4 weeks before and after treatment with administered live
vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains lactose.
323
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.
324
Utilin S
6X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Mycobacterium phlei e volumine cellulae (lyophil., steril.) 6X
Composition: 5 ml liquid dilution contain: Medically active substance: 5 ml
Mycobacterium phlei e volumine cellulae (lyophil., steril.) 6X
dil. Other constituents: puried water.
According to experience, All chronic lung diseases; chronic feverish diseases with night sweats
to be administered in and debility, subfebrile temperatures, weakness (for immune modu-
cases of: lation).
Characteristics: Utilin S
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
Do not apply to inamed skin. In cases of known hypersensitivity to
Mycobacterium phlei, as a precaution, this preparation should not
be administered.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions Immunosuppressive drugs can inuence the effectivity of Utilin S
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
325
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.
326
Utilin S
6X
Suppositories
for rectal application
Active ingredient: Mycobacterium phlei e volumine ex muris cellulae (lyophil.,
steril.) 6X
Composition: 1 suppository contains: Medically active substance: 0.2 g Myco-
bacterium phlei e volumine ex muris cellulae (lyophil., steril.)
6X trit. Other constituents: hard fat, lactose.
According to experience, All chronic lung diseases; chronic feverish diseases with night sweats
to be administered in and debility, subfebrile temperatures, weakness (for immune modu-
cases of: lation).
Characteristics: Utilin S
, theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Fever, conditions of weakness.
In cases of known hypersensitivity to Mycobacterium phlei, as a
precaution, this preparation should not be administered.
Adverse reactions: None known. Generally well tolerated. In the rst 2 or 3 days after the
application sometimes conditions of weakness, fortied expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.
Interactions Immunosuppressive drugs can inuence the effectivity of Utilin S
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains lactose.
327
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.
328
Verrukehl
5X
Drops
Liquid dilution
for oral intake, rubbing in
Active ingredient: Trichophyton verrucosum e volumine cellulae (lyophil., steril.)
5X
Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml
Trichophyton verrucosum e volumine cellulae (lyophil., steril.)
5X dil. Other constituents: puried water.
According to experience, Trichophytosis, tinea, mycosis of the skin and hair, hair loss.
to be administered in
cases of:
Characteristics: Verrukehl
; theoretically,
hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.
Contraindications: Do not administer in cases of known hypersensitivity to mold fungi
Trichophyton verrucosum.
Adverse reactions: None known.
Interactions Immunosuppressive drugs can inuence the effectivity of Verrukehl
.
with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: After opening, contents must be used within two months.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X.
329
Vitamin B Komplex Sanum N
Ampules
Liquid dilution for injection
Active ingredients: Thiamine hydrochloride (vitamin B1), pyridoxine hydrochloride
(vitamin B6)
Composition: 1 ampule of 2 ml contains: Medically active substance: 10 mg thiamine
hydrochloride (vitamin B1), 5 mg pyridoxine hydrochloride
(vitamin B6). Other constituents: benzyl alcohol.
Indication: Neuritis, neuralgia, trigeminal neuralgia, ischialgia, cervical syndrome,
herpes zoster, radiculoneuritis due to degenerative spondylopathy.
Characteristics: Vitamin B1 (thiamine) in its active form, thiamine pyrophosphate
(TPP), plays a crucial role in carbohydrate metabolism. The daily
requirement of vitamin B1 depends on the type of nutrition. If mainly
carbohydrates are consumed, then the required amount of vitamin B1
increases. A pure vitamin B1 deciency causes reduced mental and
physical power, lack of appetite and muscular atrophy, in particular
of the lower extremities. Vitamin B6 (pyridoxine) is found in all
living cells, and its effective compound, pyridoxal-5-phosphate, is an
indispensable coenzyme in amino acid metabolism. In cases of rich
protein nutrition, the vitamin B6 requirement is increased, as well as
during pregnancy and in cases of hyperthreodism. Vitamin B6 deciency
can lead to particular forms of anaemia as well as to skin diseases.
Application: Vitamin B Komplex Sanum N has to be injected slowly intravenously
or intramuscularly.
Unless otherwise prescribed: For initial treatment during the rst days
of therapy intramuscular injection daily with 1 ampule of 2 ml; after
beginning recovery, 1 ampule of 2 ml 2-3 x weekly.
Side effects: In individual cases, hypersensitivity reactions with urticaria and states
of shock, particularly in allergy prone patients, may occur.
Hypersensitivity caused by benzyl alcohol rarely develops.
Contraindications: Do not administer in cases of known vitamin B1 hypersensitivity.
Vitamin B Komplex Sanum N contains 20 mg benzyl alcohol as
preservative; therefore it must not be administered to new-born and
undeveloped premature babies.
Adverse reactions: None known.
Interactions Vitamin B1 is broken down in infusion solutions containing sulphite.
with other remedies: High dosages of Vitamin B6 can weaken the effect of L-Dopa. In case
of simultaneous use of isoniazid (INH), d-penicillamin and cycloserine,
the effect of vitamin B6 can be lowered.
330
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 2 ml ampule 10 and 50.
331
Vitamin B 12 Sanum
Ampules
Liquid dilution for injection
Active ingredient: Cyanocobalamin
Composition: 1 ampule of 1 ml contains: Medically active substance: 1 mg Cyano-
cobalamin. Other constituents: sodium chloride, sodium hydroxide
9.5 %, hydrochloric acid 5 %, isotonic sodium chloride solution.
Indications: Vitamin B12 deciency which cannot be resolved by dietary
measures. Vitamin B12 deciency can show itself in the following
disorders: hyperchromic, macrocytic megaloblastic anaemia (pernicious
anaemia, Biermers anaemia, addisonian anaemia; these are maturation
disturbances of the erythrocytes); spinal cord damage.
Vitamin B12 deciency conrmed by laboratory tests can occur in cases
of long lasting malnutrition and malnourishment (e.g. a strict vegetarian
diet); malabsorption (insufcient intestinal absorption of vitamin B12)
caused by insufcient production of intrinsic factor (a protein which is
produced by the gastric mucosa and is necessary for absorption of
vitamin B12), disorders of the ileum (a part of the small intestine), such
as sprue, sh tape worm infestation or blind loop syndrome (obstruction
of the small intestine after abdominal operations); congenital vitamin
B12 transport disorders.
Characteristics: Cyanocobalamin ist gained from bacteria cultures; therefore it is
of plant origin in contrast to hydroxycobalamin from liver extracts.
Numerous metabolic processes in the organism depend on a sufcient
vitamin B12 supply, especially the production of erythrocytes in the
bone marrow, protein synthesis (production of DNA, RNA, growth),
formation of the myelin sheath of the nerve cells, cellular detoxication,
metabolism of fatty acids and folic acid.
Application: Unless otherwise prescribed: For initial treatment during the rst weeks of
therapy 1 ampule of 1 ml Vitamin B 12 Sanum (1mg cyanocobalamin)
2 x weekly. In cases of veried intestinal malabsorption of vitamin B12,
subsequent injections with 1000g cyanocobalamin are administered
once a month.
As a rule, Vitamin B 12 Sanum is injected intramuscularly. Slow intra-
venous or subcutaneous injections are also possible.
Side effects: In individual cases, skin reactions (acne as well as eczematous urticarial
drug reactions) and hypersensitivity reactions (anaphylactic and
anaphylacticoid reactions) have occurred.
332
Contraindications: Do not administer in cases of hypersensitivity to vitamin B12 or any
other constituent.
Adverse reactions: None known.
Interactions Due to the instability of Vitamin B12, the addition of other prepara-
with other remedies: tions can lead to loss of effectiveness.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: The recommended daily vitamin B12 intake during pregnancy and
breastfeeding is 4 g. According to previous experience, higher dosages
have no adverse effects on the unborn child. Vitamin B12 passes into
breast milk.
Vitamin B 12 Sanum contains less than 1 mmol (23 mg) sodium
chloride per ampule, i.e. it is almost sodium-chloride-free.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 1 ml ampule 10 and 50.
333
Zinkokehl
3X
Drops
Liquid dilution for oral intake
Active ingredient: Zincum gluconicum 3X
Composition: 1 ml liquid dilution contains: Medically active substance: 0.08 ml
Zincum gluconicum 3X dil. Other constituents: puried water,
ethanol 15 % (m/m).
According to experience, Accompanying treatment for zinc deciency conditions: bone meta-
be administered in bolism such as coxarthrosis, pseudoarthrosis, rheumatic arthritis,
cases of: psoriatic arthritis; skin diseases such as eczema, acne, slow wound
healing, burns; susceptibility to infections; vegetative dysfunctions,
dysbiosis and consecutive diseases such as cholecystitis, pancreatitis;
diabetes mellitus; vein diseases such as thrombosis and ulcerations of
the lower leg.
Characteristics: Zinc plays a signicant role in the bodys metabolism. Chronic zinc
deciency - caused by poor nutrition or malabsorption can lead to
serious disorders. Zinkokehl
contains Zincum gluconicum and is
therefore also suitable for prophylaxis.
Application: Unless otherwise prescribed: For oral intake: in case of acute conditions
every half to one hour, not more than 6 times daily each 5 drops. In case
of chronic conditions 1-3 x daily 5 drops.
Side effects: None known.
Contraindications: None known.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: This product contains 20 % (v/v) alcohol (ethanol).
Due to the alcohol content, professional medical advice should be
sought prior to recommending this product to patients with alcohol or
liver problems.
334
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 30 ml dropper bottle 3X, 2 ml
ampule 10 and 50 4X.
335
Zinkokehl
4X
Ampules
Liquid dilution for injection
Active ingredient: Zincum gluconicum 4X
Composition: 1 ampule of 2 ml contains: Medically active substance: 2 ml Zincum
gluconicum 4X aquous dil. Other constituents: isotonic sodium
chloride solution.
According to experience, Accompanying treatment for zinc deciency conditions: bone meta-
be administered in bolism such as coxarthrosis, pseudoarthrosis, rheumatic arthritis, pso-
cases of: riatic arthritis; skin diseases such as eczema, acne, slow wound healing,
burns; susceptibility to infections; vegetative dysfunctions, dysbiosis and
consecutive diseases such as cholecystitis, pancreatitis; diabetes melli-
tus; vein diseases such as thrombosis and ulcerations of the lower leg.
Characteristics: Zinc plays a signicant role in the bodys metabolism. Chronic zinc
deciency - caused by poor nutrition or malabsorption can lead to
serious disorders. Zinkokehl
contains Zincum gluconicum and is
therefore also suitable for prophylaxis.
Application: Unless otherwise prescribed: 1 ampule of 2 ml to be injected either
intramuscularly, subcutaneously, intracutaneously or intravenously, 1-2 x
daily.
Side effects: None known.
Contraindications: None known.
Adverse reactions: None known.
Interactions
with other remedies: None known.
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Advice: None.
Duration of treatment: Dependent on the advice of the physician or health care professional.
How supplied: The following dosage forms are available: 30 ml dropper bottle 3X, 2 ml
ampule 10 and 50 4X.
336
Disease List
The following information is intended to serve as a quick reference guide for the practi-
tioner and is not intended as a prescription outline. A thorough diagnosis and individual
therapy plan is recommended in each case. It is assumed that through the participation
of seminars specialising in the eld of isopathic-homeopathy and pleomorphic research,
that the naturopath gains a clearer insight of this form of therapy.
An intensive introduction and training in SANUM therapy is possible through seminars and
corresponding literature. Contact your distributor for information on future seminars.
Abscess,
Mucokehl, Notakehl, Sanukehl Pseu, Sanu-
kehl Staph
Acidosis,
Alkala N, Citrokehl, Sanuvis
Acne,
Latensin, Mucokehl, Nigersan, Notakehl,
Pefrakehl, Polysan D, Sanukehl Myc, Sanu-
kehl Staph, Utilin, Zinkokehl
Acne vulgaris,
Sanukehl Acne
Acrodermatitis,
Notakehl, Sankombi
Acrodermatitis enterohepatica,
Fortakehl, Polysan Dx, Sanukehl Coli,
Sanukehl Myc, Zinkokehl
Actinomycosis,
Mucokehl, Notakehl, Sanukehl Myc, Sanu-
kehl Staph, Utilin S
Addisons Disease,
Mucokehl, Nigersan, Recarcin, Sankombi,
Zinkokehl
Adenoids,
Mucokehl, Nigersan, Sankombi, Utilin
Adnexitis,
Fortakehl, Mucokehl, Nigersan, Notakehl,
Pefrakehl, Sanukehl Myc, Sanukehl Strep,
Utilin
Agranulocytosis,
Citrokehl, Formasan, Notakehl, Quentakehl,
Sanukehl Pseu
Alcohol Abuse,
Alkala N, Citrokehl, Mucedokehl, Muscarsan,
Vitamin B Komplex Sanum N
Alkalinization,
Alkala N, Citrokehl, Sanuvis
Allergic Asthma,
see Allergy in general, Nigersan
Allergy in general,
Alkala N, Citrokehl, Exmykehl, Formasan,
Fortakehl, Notakehl, Polysan K, Sanuvis,
Utilin, Vitamin B Komplex Sanum N
Allergic Diseases of the Gastrointestinal tract,
see Allergy in general, Pefrakehl
Allergic Rhinitis,
Latensin, Nigersan, Notakehl, Sankombi,
Utilin
Alopecia (Baldness),
Mucokehl, Pefrakehl, Pinikehl, Sanukehl
Myc, Sanukehl Strep, Sankombi
Alopecia areata,
Mucokehl, Pinikehl, Sankombi
Amenorrhea,
Nigersan, Recarcin, Sanukehl Myc,
Ustilakehl
Amoebiasis,
Fortakehl, Okoubasan, Sanukehl Coli,
Sanukehl Salm
Anal Eczema,
Exmykehl, Fortakehl, Pefrakehl, Sanukehl
Cand
Anal Fissures,
Fortakehl, Mucokehl, Notakehl, Recarcin
Anal Fistula,
Fortakehl, Mucokehl, Nigersan, Notakehl,
Pefrakehl, Recarcin, Sanukehl Pseu, Utilin
Angina Pectoris,
Leptospermusan, Mucokehl, Nigersan,
Sanoryzae, Sanukehl Acne, Utilin
Anginal Ulcers (Acute Sore Throat),
Notakehl, Sankombi, Sanukehl Strep
337
Angioneurotic Edema,
Fortakehl, Mucedokehl, Polysan Dx,
Strophanthus
Ankle Swelling,
Leptucin, Mucokehl, Mucokehl Atox,
Strophanthus
Anorexia,
Cerivikehl, Citrokehl, Fortakehl
Anthracosis,
Formasan, Mucokehl, Polysan T, Recarcin,
Sanukehl Staph
Aphasia (see also Stroke),
Mucokehl, Sankombi, Utilin
Aphonia (see also Stroke),
Sanukehl Myc
Aphthous Ulcers,
Fortakehl, Mucokehl, Notakehl, Pefrakehl,
Quentakehl, Rebas, Recarcin, Sanukehl
Cand, Sankombi
Arrhythmia,
Mucokehl, Sanukehl Myc, Sanukehl Strep,
Strophanthus
Arteriosclerosis,
Citrokehl, Mucokehl, Nigersan, Polysan A,
Sanumgerman, Sanuvis, Utilin
Artery Disease in general,
Leptucin, Leptospermusan, Mucedokehl,
Mucokehl, Sanukehl Acne, Strophanthus
Arthritis (Osteoarthritis),
Arthrokehlan A, Latensin, Lipiscor,
Mucokehl, Nigersan, Notakehl, Polysan D,
Recarcin, Sankombi, Sanukehl Myc, Utilin,
Utilin S
Arthrosis,
Fortakehl, Latensin, Lipiscor, Notakehl,
Recarcin, Utilin S
Asthma-Bronchitis,
Fortakehl, Latensin, Mucokehl, Nigersan,
Notakehl, Sanukehl Myc, Sanukehl Klebs,
Sanukehl Pseu, Utilin, Utilin S, Vitamin B
Komplex Sanum N
Autonomic Nervous System Dysfunction,
Latensin, Mucedokehl, Utilin, Vitamin B
Komplex Sanum N, Zinkokehl
Avitaminosis,
Mapurit L, Vitamin B Komplex Sanum N
Balanitis,
Albicansan, Pefrakehl
Bed Wetting,
Citrokehl, Latensin, Mucedokehl, Sankombi,
Sanuvis, Utilin
Bladder Inammation,
see Cystitis
Bleeding Tendencies,
Calvakehl
Blepharitis,
Nigersan, Notakehl, Sanukehl Staph
Blindness,
Leptospermusan, Mucokehl, Utilin
Bloating and Flatulence,
Alkala N, Fortakehl, Pinikehl
Blood Poisoning,
Notakehl, Polysan G, Quentakehl
Breast Cancer,
Alkala N, Exmykehl, Latensin, Mucokehl,
Nigersan, Pefrakehl, Recarcin, Sanukehl
Pseu, Sanuvis, Selenokehl, Utilin
Bronchiectasis,
Formasan, Notakehl, Sanukehl Klebs
Bronchitis,
Cerivikehl, Mucokehl, Notakehl, Quentakehl,
Relivora Complex, Sankombi, Ruberkehl,
Utilin, Utilin S
Bruises,
Mucokehl, Sanuvis
Buccal Mucosal Inammation,
see Stomatitis
Burns,
Mucokehl, Notakehl, Sanukehl Pseu,
Sankombi, Zinkokehl
Candidiasis,
Albicansan, Alkala N, Exmykehl, Fortakehl,
Pefrakehl, Sanukehl Cand
Carcinoma,
Arthrokehlan U, Citrokehl, Exmykehl,
Mucokehl, Nigersan, Notakehl, Pefrakehl,
Polysan K, Polysan Om, Sankombi, Sanuvis,
Sanukehl Pseu, Sanumgerman, Selenokehl,
Utilin, Utilin S, Zinkokehl
Cataract,
Alkala N, Leptucin, Mucokehl (eye drops),
Sanuvis, Silvaysan, Utilin S
Cell Regeneration Therapy,
Chrysocor, Citrokehl, Fortakehl,
Leptospermusan, Mucokehl, Nigersan,
Sanuvis
Cephalgia,
Alkala N, Citrokehl, Quentakehl, Sanukehl
Myc, Usneabasan, Ustilakehl
338
Cervical Syndrome,
Notakehl, Quentakehl, Usneabasan, Vitamin
B Komplex Sanum N
Chickenpox,
Alkala N, Quentakehl, Sanuvis
Childhood Diseases,
Latensin, Notakehl, Pefrakehl, Sankombi,
Utilin S
Cholangitis,
Citrokehl, Fortakehl, Latensin, Mucokehl,
Notakehl, Pinikehl, Sanukehl Coli, Silvaysan,
Utilin
Cholecystitis,
Albicansan, Fortakehl, Mucokehl, Notakehl,
Pinikehl, Sanukehl Coli, Sanukehl Myc,
Utilin, Usneabasan, Zinkokehl
Chondrodystrophy,
Citrokehl, Latensin, Mapurit L, Mucokehl,
Nigersan, Utilin, Utilin S
Chronic Bronchitis,
Cerivikehl, Fortakehl, Latensin, Quentakehl,
Recarcin, Sanukehl Pseu, Utilin, Utilin S
Chronic Dermatitis (Dermopathy),
Citrokehl, Latensin, Mucokehl, Pefrakehl,
Sanukehl Pseu, Sanuvis, Utilin
Chronic Dermatosis,
Utilin, Zinkokehl
Chronic Gastrointestinal Tract Inammation,
Fortakehl, Pefrakehl, Sanukehl Salm,
Recarcin, Utilin
Chronic Hepatitis,
Pinikehl, Rebas, Sankombi, Silvaysan, Utilin
Chronic Inammation,
Fortakehl, Latensin, Notakehl, Recarcin,
Sanukehl Pseu, Utilin S
Chronic Intestinal Diseases,
Exmykehl, Fortakehl, Latensin, Sanukehl
Brucel, Sanukehl Cand, Sanukehl Coli,
Sanukehl Salm, Sanukehl Prot, Utilin
Chronicity in general,
Arthrokehlan U, Citrokehl, Fortakehl,
Lipiscor, Mapurit L, Pinikehl, Sankombi
Chronic Mucosal Inammation,
Fortakehl, Latensin, Recarcin, Relivora
Complex
Chronic Pancreatitis,
Alkala N, Citrokehl, Fortakehl, Pefrakehl,
Pinikehl, Recarcin, Sanukehl Salm
Chronic Respiratory Tract Diseases,
Citrokehl, Mucedokehl, Notakehl,
Ruberkehl, Utilin, Utilin S
Chronic Rheumatism,
Arthrokehlan A, Citrokehl, Latensin,
Notakehl, Sanukehl Pseu, Sanumgerman
Chronic Urinary Tract Infection,
Fomepikehl, Nigersan, Notakehl,
Quentakehl, Sanukehl Coli, Sanukehl Myc
Circulatory Problem of the Extremities,
Leptospermusan, Leptucin, Mucedokehl,
Mucokehl, Sanukehl Acne, Sanumgerman,
Strophanthus
Circulatory Problems in general,
Alkala N, Leptospermusan, Leptucin,
Mucokehl, Sankombi, Sanuvis
Coeliac Disease,
Exmykehl, Fortakehl, Mucokehl, Nigersan,
Notakehl, Polysan Dx, Recarcin, Sanukehl
Coli, Sanukehl Pseu, Sanukehl Salm,
Sanukehl Staph
Colds,
Notakehl, Quentakehl, Polysan G, Relivora
Komplex, Sanukehl Serra
Colitis ulcerosa Syndrome,
Albicansan, Exmykehl, Fortakehl,
Latensin, Leptospermusan, Mucokehl,
Nigersan, Notakehl, Rebas, Recarcin,
Sanukehl Brucel, Sanukehl Cand, Sanukehl
Coli, Sanukehl Myc, Utilin, Utilin S
Collagen Diseases,
Arthrokehlan A, Citrokehl, Fortakehl,
Latensin, Sanukehl Pseu, Sanuvis
Colon Cancer (see also Cacinoma),
Arthrokehlan A, Exmykehl, Fortakehl,
Latensin, Mapurit L, Mucokehl, Nigersan,
Notakehl, Pefrakehl, Recarcin, Sanukehl
Pseu, Sanuvis, Selenokehl, Utilin S
Congestive Heart Failure,
Calvakehl, Leptospermusan, Strophanthus
Conjunctivitis,
Citrokehl, Fortakehl, Leptospermusan,
Luffasan, Mucokehl (eye drops), Notakehl,
Ruberkehl, Sanukehl Myc, Sanuvis
Constipation,
Exmykehl, Fortakehl, Leptospermusan,
Mucokehl, Sanukehl Cand, Utilin
Convalescence,
see recovery
339
Coronary Circulation Problems (see
Artery Disease in general),
Leptospermusan, Leptucin, Mapurit L,
Mucokehl, Sankombi, Sanukehl Acne,
Strophanthus
Corns and Calluses,
Mucokehl, Notakehl, Sanuvis, Utilin
Crohns Disease,
Fortakehl, Latensin, Mucokehl, Nigersan,
Polysan A, Recarcin, Sanukehl Brucel,
Sanukehl Myc, Utilin S
Cystitis,
Citrokehl, Fortakehl, Leptucin, Notakehl,
Pefrakehl, Ruberkehl, Sanukehl Coll,
Sanukehl Myc, Sanuvis
Dacryocystitis,
Citrokehl, Mucokehl, Nigersan, Notakehl,
Sanukehl Staph, Sanukehl Strep
Degenerative Diseases of the Vertebrae
and the Joints,
Arthrokehlan A, Notakehl, Vitamin B
Komplex Sanum N
Dental Granuloma,
Arthrokehlan U, Notakehl, Sankombi
Dermatophytosis (Skin Fungal Infection),
Albicansan, Fortakehl, Pefrakehl, Sanukehl
Cand, Sanukehl Trich
Diabetes Mellitus,
Fortakehl, Grifokehl, Latensin, Mucokehl,
Nigersan, Sankombi, Sanukehl Coli, Utilin,
Utilin S, Zinkokehl
Diabetic Gangrene,
Leptucin, Mucokehl, Nigersan, Pinikehl,
Sankombi, Sanukehl Acne, Utilin, Utilin S
Diarrhea,
Calvakehl, Exmykehl, Fortakehl, Nigersan,
Okoubasan
Dislocation,
see distortions
Distortions,
Mucokehl, Sankombi, Sanuvis
Diverticulitis,
Fortakehl, Mucedokehl, Mucokehl, Notakehl,
Sanukehl Myc, Sanukehl Pseu, Sanuvis
Drug Abuse,
Citrokehl, Mucedokehl, Muscarsan
Dry Cough,
Cerivikehl, Notakehl, Relivora Complex
Duodenal Ulcer,
Fortakehl, Latensin, Recarcin, Sanukehl
Myc, Sanukehl Prot, Utilin S
Dupuytrens Contracture,
Mucokehl, Nigersan, Polysan Dx, Utilin
Dysbiosis,
Albicansan, Citrokehl, Fortakehl, Notakehl,
Pefrakehl, Sanukehl Myc, Sanukehl Prot,
Sanuvis, Zinkokehl
Dysfunction of the male Gonads from
diseases or aging,
Chrysocor, Citrokehl, Mucokehl, Nigersan,
Sanuvis
Dysmenorrhea,
Chrysocor, Mucedokehl, Mucokehl, Nigersan,
Recarcin, Sankombi, Ustilakehl, Utilin
Ear Inammation,
see otitis
Easy Fatigability,
Bovisan, Citrokehl, Silvaysan
Eczema,
Latensin, Notakehl, Pefrakehl, Polysan T,
Recarcin, Sankombi, Sanukehl Cand,
Sanukehl Myc, Sanukehl Strep, Sanuvis,
Utilin, Vitamin B Komplex Sanum N,
Zinkokehl
Elimination Therapy,
Luffasan, Okoubasan, Selenokehl,
Usneabasan, Zinkokehl
Embolism,
Mucokehl, Sanukehl Acne, Sanuvis, Utilin S
Empyema,
Notakehl, Sanukehl Salm, Sanukehl Staph,
Sanukehl Strep, UtilinS
Encephalitis,
Latensin, Notakehl, Quentakehl, Utilin,
Utilin S
Endocarditis,
Mucokehl, Notakehl, Quentakehl, Sanukehl
Staph, Sanukehl Strep, Utilin
Endometritis,
Alkala N, Calvakehl, Fortakehl, Mucokehl,
Nigersan, Notakehl, Sanuvis
Enteritis,
Fortakehl, Okoubasan, Pefrakehl,
Usneabasan, Utilin S
Epicondylitis,
Fortakehl, Mucokehl, Nigersan, Notakehl,
Sanuvis, Utilin, Utilin S
340
Epididymitis,
Citrokehl, Latensin, Mucokehl, Nigersan,
Notakehl, Quentakehl, Sanukehl Coli,
Sanukehl Myc
Epilepsy,
Mucedokehl, Mucokehl, Muscarsan,
Nigersan, Sanumgerman, Utilin
Erysipelas,
Latensin, Notakehl, Quentakehl, Sanukehl
Strep, Utilin
Erythema nodosum,
Bovisan, Sanukehl Strep, Utilin S
Extrapulmonary Tuberculosis,
Nigersan, Sanukehl Myc, Utilin S
Exudative Erythema Multiforme,
Nigersan, Utilin S
Eye (Inammation of),
Mucokehl, Mucokehl (eye drops), Notakehl
Femoral Artery and Vein Diseases (see
Artery Diseases in general),
Mucokehl, Sanukehl Acne, Sanuvis
Fever,
Larikehl, Notakehl, Polysan G, Quentakehl,
Relivora Complex, Utilin S
Fibromyalgia,
Fortakehl, Latensin, Quentakehl, Sanukehl
Myc, Sanukehl Pseu
Fissures,
see rhagades
Flatulence and Bloating,
Alkala N, Fortakehl, Pinikehl
Folliculosis,
Mapurit L, Notakehl, Sanukehl Staph
Food Poisoning,
Okoubasan
Fractures,
Citrokehl, Mucokehl, Nigersan, Sanuvis,
Utilin, Zinkokehl
Frequent Infections,
(see Susceptibility to Infection)
Fortakehl, Sankombi, Utilin, Zinkokehl
Frostbite,
Leptucin, Mucokehl, Nigersan, Sanuvis, Utilin
Functional Heart Complaints,
Fortakehl, Mucokehl, Sanuvis, Strophanthus
Fungal Infections in general,
Albicansan, Exmykehl, Fortakehl, Nigersan,
Notakehl, Pefrakehl, Sanukehl Cand
Furunculosis (Boils),
Latensin, Mucokehl, Notakehl, Sanukehl
Pseu, Sanukehl Salm, Sanukehl Staph, Utilin
Gallbladder Disease,
Alkala N, Fortakehl, Latensin, Pinikehl,
Recarcin, Silvaysan, Utilin
Ganglion Cyst,
Latensin, Nigersan, Recarcin, Sankombi,
Sanuvis, Utilin
Gastric Mucosal Diseases,
Alkala N, Fortakehl, Latensin, Recarcin,
Sanukehl Prot
Gastric Mucosal Inammation,
see gastritis
Gastric Ulcer,
Alkala N, Fortakehl, Latensin, Mucokehl,
Recarcin, Sanukehl Myc, Sanukehl Prot,
Sanuvis, Utilin
Gastritis,
Alkala N, Fortakehl, Latensin,
Leptospermusan, Mucedokehl, Mucokehl,
Recarcin, Sanukehl Myc, Sanukehl Prot,
Sanuvis, Utilin
Gastroenteritis,
Citrokehl, Fortakehl, Latensin, Okoubasan,
Pefrakehl, Sanukehl Coli, Sanukehl Salm
Gastrointestinal Dysfunction,
Citrokehl, Fortakehl, Pefrakehl, Pinikehl,
Okoubasan, Sanuvis
Gastrointestinal Tract Disease,
Alkala N, Calvakehl, Fortakehl, Latensin,
Leptospermusan, Mucokehl, Rebas,
Recarcin, Sanuvis, Utilin
Gastrointestinal Tract Infection,
Fortakehl, Okoubasan, Quentakehl
Gastrointestinal Tract Inammation,
Fortakehl, Latensin, Recarcin, Sanukehl Prot
Generalized Itchiness
(see Allergy in general),
Fortakehl, Pefrakehl, Sanukehl Cand,
Sanukehl Pseu, Sanuvis
Genital Herpes (see Herpes in general),
Alkala N, Latensin, Mucokehl, Nigersan,
Quentakehl, Sanukehl Prot, Stolonikehl
Genital Itchiness,
Albicansan, Alkala N, Fortakehl, Pefrakehl,
Sanukehl Cand, Silvaysan
Genital Mycosis (see mycosis in general),
Albicansan, Exmykehl, Pefrakehl, Sanukehl
Cand
341
Gingivitis,
Albicansan, Fortakehl, Latensin, Mucokehl,
Nigersan, Notakehl, Pefrakehl, Sanukehl
Cand, Utilin
Glaucoma,
Mucokehl, Mucokehl (eye drops), Sanuvis,
Utilin S
Gonorrhea,
Notakehl, Polysan E, Utilin S
Gout,
Alkala N, Mucokehl, Recarcin, Sankombi,
Sanuvis, Utilin
Graves Disease (Exophtalmic Goiter),
Latensin, Mucokehl, Nigersan, Notakehl,
Sankombi, Utilin, Utilin S
Growth and Developmental Disorders,
Citrokehl, Fortakehl, Sanukehl Salm,
Thymokehl
Hair loss (see Alopecia),
Notakehl, Pleo Chelate, Sanukehl Myc,
Sanukehl Trich, Selenokehl, Vitamin B
Komplex Sanum N, Zinkokehl
Hay Fever (see Allergy in general),
Luffasan, Ruberkehl, Sanukehl Pseu,
Headache,
see cephalgia
Heartburn,
Alkala N, Fortakehl, Sanukehl Myc,
Sanukehl Strep, Strophanthus
Heavy metal burden,
Mapurit L, Okoubasan, Pleo Chelate,
Selenokehl, Usneabasan, Zinkokehl
Hematoma (Bruises),
Mucokehl, Sanuvis
Hemiplegia,
Leptucin, Mucokehl, Sankombi, Sanukehl
Acne, Sanuvis, Utilin
Hemorrhagic Rhinitis,
Calvakehl, Mucokehl, Sanuvis, Ustilakehl
Hemorrhoids,
Mucokehl, Notakehl, Sanuvis
Hepatitis B,
Fortakehl, Leptucin, Pinikehl, Rebas,
Sankombi, Silvaysan, Utilin
Herpes in general,
Latensin, Notakehl, Quentakehl, Sankombi,
Sanukehl Prot, Stolonikehl, Vitamin B
Komplex Sanum N
Herpes zoster,
Notakehl, Quentakehl, Sanukehl Prot,
Sanuvis, Stolonikehl, Vitamin B Komplex
Sanum N
Hodgkins Lymphogranulomatosis,
Latensin, Mucokehl, Nigersan, Notakehl,
Sanukehl Pseu, Sanuvis, Utilin
Hydrocoele,
Nigersan, Notakehl, Sanukehl Myc
Hyperlipidemia,
Lipiscor, Mucokehl, Nigersan, Sanuvis
Hypertension,
Lipiscor, Mucokehl, Utilin, Sanoryzae,
Sanuvis
Hyperthyroidism,
Mucokehl, Nigersan, Notakehl, Sankombi,
Utilin, Utilin S
Hyperthrophy of the Tonsils,
Bovisan, Mucokehl, Nigersan, Notakehl
Hypogonadism,
Chrysocor, Citrokehl, Mucokehl, Nigersan
Hypotension,
Mucokehl, Polysan K, Selenokehl,
Utilin S
Hypoxia,
Calvakehl
Ichthyosis (Dry scaly skin),
Nigersan, Notakehl, Sankombi, Sanuvis,
Utilin, Utilin S
Immunomodulation,
Arthrokehlan U, Bovisan, Episcorit,
Fomepikehl, Grifokehl, Latensin, Leptucin,
Recarcin, Relivora Complex, Sanukehl Pseu,
Utilin, Utilin S
Impetigo,
Latensin, Notakehl, Sanukehl Staph, Utilin,
Utilin S
Induratio penis,
Mucokehl, Nigersan, Sanuvis
Infarct, Status post,
Leptucin, Mucokehl, Sankombi, Sanukehl
Acne, Sanukehl Strep, Sanuvis
Infectious Diseases,
Alkala N, Fortakehl, Notakehl, Quentakehl,
Sanuvis
Infectious Skin Disease,
Albicansan, Notakehl, Pefrakehl, Sanuvis,
Utilin
342
Infertility,
Chrysocor, Fortakehl, Latensin, Mucokehl,
Nigersan, Sankombi, Sanuvis, Selenokehl
Inammation after BCG Vaccination,
Bovisan, Citrokehl, Nigersan
Inammation in general,
Latensin, Leptospermusan, Mucokehl,
Notakehl, Polysan G, Rebas
Inammation of the Biliary Tract,
Citrokehl, Fortakehl, Latensin, Mucokehl,
Notakehl, Pinikehl, Sanukehl Coli, Sanukehl
Myc, Utilin
Inammation of the Digestive Organs
(see gastritis, Crohns Disease, Colitis
ulcerosa),
Fortakehl, Larikehl, Latensin, Mucokehl,
Sanukehl Myc, Sanukehl Pseu, Sanuvis,
Utilin
Inammatory Process of the Stomach,
Citrokehl, Cuprukehl, Fortakehl, Latensin,
Notakehl, Recarcin, Sanukehl Prot
Inuenza Infection,
Polysan G, Quentakehl, Ruberkehl,
Sanukehl Klebs, Sanuvis
Inherited Toxins,
Polysan E, Utilin S
Insect Bites,
Notakehl, Sankombi, Sanukehl Pseu,
Sanuvis
Intercostal Neuralgia,
Citrokehl, Notakehl, Quentakehl, Sanuvis,
Stolonikehl
Intermittent Claudication,
see smokers Leg
Intermittent Fever,
Pinikehl, Polysan M, Sanukehl Brucel
Intestinal Dysfunction,
Fortakehl, Utilin
Intestinal Yeast Infection,
Albicansan, Exmykehl, Fortakehl,
Pefrakehl, Sanukehl Cand
Intestinal Tuberculosis,
Citrokehl, Latensin, Nigersan, Sanukehl
Myc, Utilin S
Intoxication,
Okoubasan
Iridocyclitis,
Mucokehl, Nigersan, Notakehl, Sanuvis
Joint Diseases,
Latensin, Notakehl, Recarcin, Sanukehl
Strep
Keloid,
Mucokehl, Sanukehl Pseu
Keratitis,
Mucokehl, Sanukehl Myc
Kraurosis vulvae,
Citrokehl, Nigersan, Sanukehl Myc
Landry Palsy (Guillian Barre Syndrome),
Exmykehl, Lipiscor, Notakehl, Quentakehl,
Sankombi, Utilin S, Vitamin B Komplex
Sanum N
Laryngeal Ulceration,
Notakehl, Quentakehl, Recarcin, Sanukehl
Myc
Laryngitis,
Cerivikehl, Nigersan, Notakehl, Quentakehl
Leg Cramps,
Latensin, Mapurit L, Mucokehl
Leukemia,
Citrokehl, Mucokehl, Nigersan, Sankombi,
Sanuvis
Leukopenia,
Latensin, Mucokehl, Nigersan, Pinikehl,
Sanukehl Pseu, Sanuvis
Libido Problems,
Chrysocor, Citrokehl, Ginkgobakehl,
Mapurit L, Nigersan, Selenokehl
Lichen ruber (Acuminatus Pityriasis),
Latensin, Mucokehl, Nigersan, Sanukehl
Trich, Sanuvis, Utilin, Zinkokehl
Lipomatosis, Lipomas,
Citrokehl, Latensin, Lipiscor, Mucokehl,
Nigersan, Recarcin, Sanuvis, Utilin S
Liver Cancer (see Carcinoma),
Chrysocor, Exmykehl, Latensin, Lipiscor,
Mucokehl, Nigersan, Recarcin, Sanukehl
Pseu, Sanuvis
Liver Cirrhosis,
Citrokehl, Mucokehl, Nigersan, Notakehl,
Pinikehl, Recarcin, Sanuvis, Silvaysan
Liver Disease,
Alkala N, Latensin, Notakehl, Pinikehl,
Rebas, Sankombi, Sanuvis, Silvaysan,
Utilin
Liver Parenchymal Disorder,
Sankombi, Selenokehl, Silvaysan, Utilin
343
Lobar Pneumonia
(see Pneumonia in general),
Citrokehl, Fortakehl, Nigersan, Notakehl,
Polysan Dx, Polysan T, Sanukehl Klebs,
Sanukehl Staph
Low Energy/Performance Levels,
Chrysocor, Citrokehl, Mapurit L, Selenokehl
Lumbago,
Notakehl, Nigersan, Recarcin, Utilin,
Vitamin B Komplex Sanum N
Lung Abscess,
Larikehl, Mucokehl, Notakehl, Sanukehl
Myc, Sanukehl Pseu
Lung Cancer,
Fortakehl, Mucokehl, Nigersan, Notakehl,
Pefrakehl, Recarcin, Sankombi, Sanukehl
Myc, Sanukehl Pseu, Sanuvis, Utilin S
Lung Diseases,
Cerivikehl, Citrokehl, Larikehl, Nigersan,
Notakehl, Utilin S
Lung Emphysema,
Fortakehl, Larikehl, Latensin, Mucokehl,
Nigersan, Sanukehl Myc, Utilin
Lupus,
Fortakehl, Latensin, Mucokehl, Nigersan,
Pefrakehl, Recarcin, Sanukehl Myc, Sanuvis,
Utilin, Utilin S
Lyme Disease/Borreliosis,
Alkala N, Fortakehl, Mucokehl, Nigersan,
Notakehl, Sanukehl Brucel, Utilin S
Lymphadenitis (Lymph Node Swelling),
Latensin, Mucokehl, Nigersan, Notakehl,
Pefrakehl, Recarcin, Sanoryzae, Sanuvis,
Utilin S
Lymphatic Constitution,
Nigersan, Pefrakehl, Sankombi, Sanoryzae,
Sanuvis
Lymphoma,
Latensin, Mucokehl, Nigersan, Sankombi,
Utilin
Lymphostasis,
Mucedokehl, Mucokehl, Nigersan
Magnesium Deciency (Malabsorbtion),
Mapurit L
Malaria, Status Post,
Citrokehl, Fortakehl, Mucokehl, Nigersan,
Notakehl, Polysan M, Sanukehl Brucel,
Sanuvis, Utilin S
Male Menopausal Syndrome,
Alkala N, Chrysocor, Mucedokehl, Nigersan,
Sanuvis, Silvaysan
Malignant Melanoma,
see carcinoma
Mastitis,
Mucokehl, Notakehl, Sanukehl Staph,
Sanukehl Strep
Mastoiditis,
Mucokehl, Nigersan, Notakehl, Sanukehl
Staph
Measles,
Notakehl, Quentakehl, Utilin
Menires Disease,
Mucokehl, Quentakehl, Sanukehl Prot
Meningitis,
Latensin, Notakehl, Quentakehl, Sanukehl
Staph, Sanukehl Strep, Utilin S
Menopausal Symptoms,
Mucokehl, Sankombi, Ustilakehl, Utilin
Menorrhagia (Excessive Menstruation),
Calvakehl, Ustilakehl
Metabolic Disorders,
Citrokehl, Mapurit L, Polysan A, Sanuvis,
Selenokehl, Silvaysan
Metritis (Inammation of the Uterus),
Fortakehl, Notakehl, Sankombi, Sanukehl
Coll, Sanukehl Myc
Metrorrhagia (Uterine Bleeding),
Calvakehl, Ustilakehl
Middle Ear Infections,
see otitis media
Migraine,
Alkala N, Latensin, Leptospermusan,
Luffasan, Mucokehl, Quentakehl,
Polysan T, Sanukehl Strep, Sanuvis,
Selenokehl, Silvaysan, Usneabasan,
Ustilakehl
Mouth Diseases,
Albicansan, Notakehl, Pefrakehl, Sanukehl
Cand, Sanukehl Myc
Multiple Sclerosis,
Exmykehl, Latensin, Mucokehl, Nigersan,
Notakehl, Pleo Chelate, Quentakehl,
Recarcin, Sanumgerman, Sanuvis,
Stolonikehl, Utilin
344
Myalgia (Muscle Pains),
Arthrokehlan A, Larikehl, Mapurit L,
Sanukehl Brucel, Sanuvis, Vitamin B
Komplex Sanum N
Mycosis in general,
Albicansan, Exmykehl, Nigersan, Notakehl,
Sankombi, Pefrakehl, Sanukehl Cand
Myocardial Infarction,
Alkala N, Leptospermusan, Mucokehl,
Sanukehl Acne, Sanuvis
Myocarditis,
Mucokehl, Notakehl, Quentakehl, Sanukehl
Strep
Nasal Mucosa Inammation,
Luffasan, Mucedokehl, Notakehl,
Quentakehl, Recarcin, Ruberkehl
Nephritis,
Cuprukehl, Latensin, Mucokehl, Nigersan,
Notakehl, Quentakehl, Ruberkehl,
Sankombi, Sanukehl Myc, Sanukehl Staph,
Sanuvis, Utilin
Nephrosis,
Latensin, Notakehl, Pefrakehl, Quentakehl,
Ruberkehl, Sanuvis
Nerve Inammation,
see neuritis
Neuralgia,
Mapurit L, Notakehl, Polysan R, Quentakehl,
Selenokehl, Vitamin B Komplex Sanum N
Neurodermatitis,
Fortakehl, Latensin, Mucokehl, Nigersan,
Notakehl, Sanuvis, Utilin, Utilin S
Neuromuscular Disorders,
Cerivikehl, Latensin, Mapurit L, Okoubasan
Neuropathy,
Mucedokehl, Notakehl, Polysan A, Sanukehl
Acne, Selenokehl, Stolonikehl
Neuritis,
Mapurit L, Mucokehl, Notakehl, Recarcin,
Sankombi, Utilin, Utilin S, Vitamin B
Komplex Sanum N, Zinkokehl
Nodules,
Sanukehl Coli, Utilin
Nose Bleeding,
Calvakehl
Obesity,
Alkala N, Grifokehl, Latensin, Mucedokehl,
Muscarsan, Nigersan, Utilin, Utilin S
Oophoritis (Inammation of the Ovaries),
Mucokehl, Notakehl, Quentakehl, Recarcin
Osteochondritis,
Citrokehl, Latensin, Nigersan, Notakehl,
Utilin
Osteochondrosis,
Latensin, Nigersan, Notakehl, Sanukehl
Myc, Utilin S
Osteomyelitis,
Mucokehl, Notakehl, Quentakehl, Sanukehl
Prot, Sanukehl Staph, Sanukehl Strep,
Utilin S
Osteoporosis,
Alkala N, Citrokehl, Fortakehl, Latensin,
Nigersan, Recarcin, Sankombi, Sanuvis,
Utilin
Ostitis,
Citrokehl, Mucedokehl, Mucokehl, Notakehl,
Sankombi, Sanuvis, Utilin
Otitis externa,
Notakehl, Pefrakehl
Otitis media,
Mucokehl, Nigersan, Notakehl, Recarcin,
Sanukehl Pseu, Sanukehl Strep, Sankombi,
Utilin
Otosclerosis,
Citrokehl, Mucokehl, Nigersan, Polysan E,
Utilin
Ovarian Cyst,
Citrokehl, Mucokehl, Nigersan, Utilin,
Utilin S
Pancreatic Insufciency,
Alkala N, Citrokehl, Fortakehl, Nigersan,
Pinikehl, Silvaysan
Pancreatitis,
Fortakehl, Mucokehl, Nigersan, Notakehl,
Quentakehl, Recarcin, Sanuvis, Zinkokehl
Paradentosis,
Citrokehl, Nigersan, Notakehl, Pefrakehl,
Pleo Chelate, Polysan A
Paratubercular Inammation,
Bovisan, Fortakehl, Nigersan, Sankombi,
Utilin
Parkinsons Disease,
Fortakehl, Latensin, Leptucin, Mapurit L,
Mucedokehl, Mucokehl, Nigersan, Sanukehl
Acne, Utilin
345
Pemphigus vulgaris,
Mucokehl, Pefrakehl, Quentakehl, Utilin S
Perianal Eczema,
Pefrakehl, Utilin, Albicansan
Pericarditis,
Mucokehl, Notakehl, Quentakehl, Sanukehl
Strep, Strophanthus
Peripheral Vascular Disease,
Ginkgobakehl, Leptospermusan, Leptucin,
Mucokehl, Sanukehl Acne, Sanukehl Prot
Peritonsillitis,
Notakehl, Sanukehl Prot
Pernicious Anemia,
Fortakehl, Mucokehl, Sanuvis, Utilin,
Vitamin B Komplex Sanum N
Perthess Disease,
Citrokehl, Latensin, Nigersan, Utilin
Pertussis,
Quentakehl, Recarcin, Relivora Complex,
Ruberkehl
Peyronies Disease,
see lnduratio penis
Pharyngitis,
Notakehl, Quentakehl, Sanukehl Pseu,
Utilin S
pH Regulation,
Alkala N, Citrokehl, Sanuvis
Pleuritis,
Nigersan, Notakehl, Sanukehl Myc,
Sanukehl Klebs
Pneumoconiosis,
Notakehl, Sanukehl Klebs
Pneumonia,
Citrokehl, Nigersan, Notakehl, Sanukehl
Coli, Sanukehl Klebs, Sanukehl Staph,
Sanukehl Strep, Utilin
Polyarthritis,
Larikehl, Mucokehl, Nigersan, Notakehl,
Recarcin, Sanukehl Brucel, Sanukehl Myc,
Sanuvis, Utilin S
Poor Bone and Cartilage Growth and
Healing,
Nigersan, Selenokehl, Utilin, Zinkokehl
Post Alcohol Abuse,
Muscarsan, Alkala N, Mucedokehl, Citrokehl
Post Menopausal Syndrome,
Chrysocor, Ustilakehl, Utilin
Precancerous Stages,
Fortakehl, Mapurit L, Polysan Om,
Sanukehl Pseu, Selenokehl, Utilin S,
Zinkokehl
Pre- and Post-operative Phase,
Chrysocor, Cuprukehl, Mucokehl, Sanuvis
Pregnancy,
Sankombi, Sanuvis
Problems of the Elderly,
Chrysocor, Citrokehl, Latensin, Mucokehl,
Nigersan, Polysan A, Sankombi, Sanuvis,
Selenokehl, Utilin
Progressive Chronic Polyarthritis,
see rheumatoid arthritis
Prostatic Adenoma and Hypertrophy,
Exmykehl, Fomepikehl, Mucokehl, Nigersan,
Notakehl, Sanuvis
Prostatic Cancer,
Exmykehl, Fomepikehl, Mucokehl, Nigersan,
Notakehl, Sankombi, Sanukehl Pseu
Prostatitis,
Exmykehl, Mucokehl, Nigersan, Notakehl,
Pefrakehl, Polysan A, Sanukehl Coli
Psoriasis,
Fortakehl, Latensin, Mucokehl, Notakehl,
Recarcin, Sanukehl Myc, Sanuvis, Utilin,
Utilin S
Psoriatic Arthritis,
Fortakehl, Larikehl, Latensin, Recarcin,
Utilin S, Zinkokehl
Pyelocystitis and -nephritis,
Citrokehl, Nigersan, Notakehl, Sanukehl
Coli, Sanukehl Myc, Sanukehl Prot, Sanuvis
Pyloric Spasm,
Fortakehl, Leptospermusan, Mucedokehl
Pyoderma,
Mucokehl, Notakehl, Pefrakehl, Sankombi,
Utilin
Raynauds Disease,
Leptucin, Mucokehl, Sanukehl Acne,
Sanuvis
Recovery,
Latensin, Mucokehl, Zinkokehl
Rectal Cancer,
see Carcinoma
Reiters Disease,
Fortakehl, Latensin, Mucokehl, Notakehl,
Recarcin, Utilin
346
Respiratory Diseases,
Alkala N, Cerivikehl, Citrokehl, Formasan,
Latensin, Luffasan, Mucedokehl, Notakehl,
Sankombi, Sanukehl Klebs
Respiratory Inammation,
Notakehl, Quentakehl, Relivora Complex
Rheumatic Fever (see Rheumatism),
Fortakehl, Notakehl, Sanukehl Salm
Rheumatism,
Alkala N, Arthrokehlan A, Bovisan,
Citrokehl, Latensin, Mucokehl, Nigersan,
Polysan R, Polysan T, Recarcin, Sankombi,
Utilin, Utilin S, Vitamin B Komplex
Sanum N
Rheumatoid Arthritis,
Fortakehl, Latensin, Nigersan, Notakehl,
Recarcin, Sanukehl Acne, Utilin, Vitamin B
Komplex Sanum N, Zinkokehl
Rhinitis,
Fortakehl, Latensin, Luffasan, Mucokehl,
Nigersan, Quentakehl, Recarcin, Ruberkehl,
Sanukehl Myc, Sanuvis, Utilin
Salpingitis,
Notakehl, Sanukehl Coli
Scarlet Fever,
Mucokehl, Notakehl, Sanukehl Strep,
Utilin
Scheuermanns Disease,
Citrokehl, Latensin, Mucokehl, Nigersan,
Sanuvis
Sciatica (Sciatic Nerve Pain),
Mucokehl, Notakehl, Utilin, Vitamin B
Komplex Sanum N
Scintillating Scotoma,
Mucokehl (eye drops)
Septic Fever,
Alkala N, Citrokehl, Fortakehl, Nigersan,
Notakehl, Pefrakehl, Pinikehl, Quentakehl,
Sanuvis
Silicosis,
Citrokehl, Mucokehl, Nigersan, Sanukehl
Klebs
Sinubronchitis,
Fortakehl, Latensin, Mucedokehl, Nigersan,
Notakehl
Sinusitis,
Cerivikehl, Luffasan, Mucedokehl, Notakehl,
Pinikehl, Quentakehl, Ruberkehl, Sanukehl
Pseu, Sanukehl Staph, Utilin S
Skin and Conjunctival Tuberculosis,
Nigersan, Sanukehl Acne, Utilin S
Skin Diseases,
Calvakehl, Pefrakehl, Sanuvis, Utilin,
Zinkokehl,
Sleep Disturbance,
Fortakehl, Leptospermusan
Smokers Leg,
Leptucin, Mucokehl, Sanukehl Acne,
Sanuvis
Spherocytosis,
Fortakehl, Mucokehl, Nigersan, Pefrakehl,
Vitamin B Komplex Sanum N
Spleen Diseases,
Mucokehl, Okoubasan, Pinikehl, Sanuvis
Spondylopathy,
Citrokehl, Latensin, Nigersan, Notakehl,
Quentakehl
Sprains,
Mucokehl
Stimulation of Blood Cell Production,
Citrokehl, Leptucin, Mucokehl, Sanuvis
Stomatitis,
Albicansan, Notakehl, Pefrakehl,
Quentakehl, Recarcin, Sanukehl Cand,
Utilin
Stroke,
Leptospermusan, Leptucin, Mucokehl,
Sanukehl Acne, Sanuvis, Utilin
Stye,
Notakehl, Sanukehl Myc, Sanukehl Staph
Sunstroke,
Usneabasan, Mucokehl, Sanuvis
Suppurations,
Notakehl, Polysan G
Susceptibility to Infection,
Fortakehl, Quentakehl, Sankombi, Sanukehl
Serra, Utilin S
Symbiotic Therapy (Symbiosis)
(see Dysbiosis),
Fortakehl, Pefrakehl, Sanukehl Coli
Swelling,
Mucokehl, Sanuvis
Tennis Elbow,
see epicondylitis
Tension Headaches,
Muscarsan, Quentakehl, Usneabasan
347
Thromboangiitis obliterans
(Buergers disease),
Citrokehl, Mucokehl, Nigersan, Notakehl,
Sanuvis, Utilin S
Thrombophlebitis,
Mucokehl, Notakehl, Sanukehl Myc,
Sanuvis, Utilin
Thrombosis,
Mucokehl, Sanuvis, Utilin, Zinkokehl
Thyroid Disease and Dysfunction,
Citrokehl, Fortakehl, Latensin, Mucedokehl,
Nigersan, Pleo Chelate, Recarcin, Sanukehl
Myc, Sanukehl Prot, Sanuvis, Utilin,Utilin S
Tinea,
Pefrakehl, Sanukehl Trich
Tinnitus,
Citrokehl, Latensin, Leptucin, Mucokehl,
Nigersan, Notakehl, Sanuvis, Utilin
Tonsillitis,
Mucedokehl, Notakehl, Polysan G,
Sankombi, Sanukehl Staph, Sanukehl Strep,
Utilin
Tooth Abscess,
Arthrokehlan A, Notakehl
Transient Ischemic Attacks,
Alkala N, Mucokehl, Leptospermusan,
Sanuvis
Trichomycosis (Fungal infection of the
hair) and Trichophytosis (Tinea barbae),
Notakehl, Pefrakehl, Sankombi, Sanukehl
Trich, Utilin S
Trigeminal Neuralgia,
Leptospermusan, Stolonikehl, Vitamin B
Komplex Sanum N
Tubal Cyst,
Citrokehl, Mucokehl, Nigersan, Utilin
Tubercular Rheumatism,
Bovisan, Citrokehl, Nigersan, Sanum-
german, Utilin S
Tuberculoid Skin Problem,
Citrokehl, Nigersan, Polysan T, Utilin,
Utilin S
Tuberculosis in general,
Bovisan, Chrysocor, Citrokehl, Latensin,
Nigersan, Polysan T, Sanukehl Myc, Utilin,
Utilin S
Tumors,
see Carcinoma
Ulcus cruris,
Leptucin, Mucokehl, Notakehl, Sanukehl
Myc, Sanukehl Pseu, Sanuvis, Zinkokehl
Upper Abdominal Complaints,
Fortakehl, Latensin, Mucokehl, Recarcin,
Utilin S
Urethritis,
Albicansan, Mucokehl, Nigersan, Notakehl,
Pefrakehl, Sanukehl Staph, Sanukehl Myc
Urinary Tract Infection,
Fortakehl, Latensin, Nigersan, Notakehl,
Pefrakehl, Sanukehl Coll, Sanukehl Myc
Urticaria,
Formasan, Fortakehl, Latensin, Mucokehl,
Nigersan, Sanukehl Myc, Sanuvis, Utilin,
Utilin S
Uterine Bleeding,
Calvakehl, Ustilakehl
Uterine Myoma,
Mucokehl, Nigersan, Selenokehl, Utilin S
Vaginal Discharge,
Albicansan, Notakehl, Pefrakehl, Sankombi,
Recarcin, Sanuvis
Vaginitis,
Albicansan, Grifokehl, Notakehl, Pefrakehl,
Quentakehl, Sanukehl Cand, Sanukehl Coli,
Sanukehl Myc
Varicose Veins,
Mucokehl, Nigersan, Polysan K, Sanuvis
Vascular Migraine,
Leptospermusan, Leptucin, Quentakehl,
Sanoryzae, Selenokehl
Vascular System Complaints,
Mucokehl
Veins Diseases,
Mucokehl, Polysan K, Sankombi, Zinkokehl
Vertigo,
Luffasan, Mucokehl, Quentakehl
Vitiligo,
Citrokehl, Mucokehl, Nigersan, Sanuvis,
Utilin S
Viral Infections,
Citrokehl, Grifokehl, Leptospermusan,
Notakehl, Quentakehl, Sanuvis
Vitamin E Deciency,
Mapurit L
Vomiting,
Fortakehl
348
Vomiting of blood,
Calvakehl, Fortakehl, Sanukehl Prot
Vulvovaginitis,
Albicansan, Notakehl, Pefrakehl,
Quentakehl, Sanukehl Cand
Warts,
Citrokehl, Latensin, Quentakehl, Mucokehl,
Nigersan, Sanuvis, Utilin S
Weak Immune System,
see Immunomodulation
Whooping Cough,
see Pertussis
Wound Healing Problems,
Mucokehl, Sankombi, Zinkokehl
Yeast Infection of the Vagina,
Albicansan, Alkala N, Citrokehl, Exmykehl,
Fortakehl, Pefrakehl, Recarcin, Sanukehl
Cand
349
Notes:
350
Notes:
351
Notes:
352
Notes:
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