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Forensic Tutorial 2012 (MyPSA)

1. The following are the provisions of the relevant pharmacy legislations pertaining to
psychotropic substances:

I Listed under third schedule of the PA 1952


II May be sold or supplied via a prescription
III To be recorded in the Prescription Book
IV May be disposed by the hospital pharmacist only

A I and II only
B I, II and III only
C I, III and IV only
D All of above

2. Records of importation for Methadone Pulv. B.P. shall be in

I Supply register for Psychotropic substance


II Part I Register for Dangerous Drug
III Part II Register Dangerous Drug
IV Poisons wholesale Sales Book

A I only
B II only
C III only
D IV only

3. By virtue of the provisions of the relevant pharmacy legislations, the following


statement is TRUE of licensed pharmacists:

I To possess and supply to a patient, group B poisons and psychotropic


substance.
II To import, manufacture and sell by wholesale any poison and psychotropic
substance.
III To dispense, compound and mix any poison and psychotropic substance
IV To hold the keys to the place of storage of any poison and psychotropic
substance

A II only
B II and III only
C II, III, IV only
D All of the above

4. Labeling for the supply of Pethidine Tablet for medical treatment of a patient at a
government hospital shall comply with the labeling requirements for

I Psychotropic Substances
II Dangerous Drug
III Dispensed Medicine
IV Poisons

A I only
B II only
C III only
D IV only
5. The following are the functions of the authorities under the relevant pharmacy
legislations:

I Poison Board classifies poisons list


II Medicine Advertisement Board approves advertisements on body conditions
of human beings
III Drug Control Authority registers products and issues licenses to any person
to import, manufacture and sell by wholesale the products
IV Licensing Officer may revoke licenses previously issued

A I only
B II and IV only
C I, III and IV only
D All of the above

6. According to the provisions of the relevant pharmacy legislations, the following statement is
TRUE of registered pharmacists in a government hospital:

I To possess and supply group B poisons and psychotropic substances


II To import, manufacture and supply by wholesale any poisons and psychotropic
substance
III To dispense, compound and mix any poisons and psychotropic substance
IV To hold the keys to the place of storage of any poisons and psychotropic substance

A II only
B II and III only
C II, III and IV only
D None of the above

7. The following are the powers of officers under the relevant pharmacy legislations:

I Drug Enforcement Officer may examine orally any person acquainted with the
commission of an offence
II Officers and inspectors may seize products which are not registered
III Authorized office may seize documents which are related to the publication of any
treatment of body conditions
IV Drug Enforcement Officer may prosecute any person who contravenes the
Dangerous Drugs Act 1952

A I only
B I and III only
C I, II and III only
D All of the above

8. The following are exemptions from the application of the relevant pharmacy legislations in
relation to Syrup Methadone (a registered product):

I Government pharmacist may import without import authorization


II The supply is exempted from Dangerous Drug Regulations 1952
III No fee is imposed for importing by a government pharmacist
IV Pharmacy assistants in government health clinic may possess and supply

A I and II only
B I, II and III only
C II and III only
D II, III and IV only
9. The following are the provisions of the relevant pharmacy legislations for dangerous drugs:

I Listed under the First Schedule of the Dangerous Drug Act 1952
II Products listed under Third Schedule of the Dangerous Drugs Regulations 1952 are
exempted from the provisions
III Part I register is the record for obtaining the raw materials
IV All products containing dangerous drugs are also listed under Third Schedule of the
Poisons Act 1952

A I only
B I, II and III only
C I, III and IV only
D All of the above

10. The following are reasons for prohibitory order by the Minister:

I A registered pharmacist who has been convicted of an offence relating to


psychotropic substances
II A registered medical practitioner who is prescribing, administering or supplying or
directing the administration of psychotropic substances in an irresponsible manner
III Psychotropic substances are given free of charge in return for large purchase
IV Allowing pharmacy assistants in government health clinic to supply psychotropic
substances

A I and II only
B I, II and III only
C II, III and IV only
D All of the above

Referring to the Medicines(Advertisement and Sale) Act 1956, read the following pamphlet
before attempting to answer QUESTIONS NO.11 TO NO.13:

BANGI FOOT REFLEXOLOGY

Effective Cure for:


Shoulder, back, head & neck pain, foot numbness, tendon sprain

Qi Sdn. Bhd
Lot 404, Bangi, Selangor
Tel: 016-4044040

11. The following are the provisions in the control of the advertisement:

I It refers to publication of a product for prevention, treatment or diagnosis of a disease


or body conditions
II The Medicines Advertisement Board may give approval for such advertisement after
application and payment of certain fees
III Advertisement of such skill or services may be allowed after the Minister has given
exemption
IV The authorized officer may prosecute Qi Sdn. Bhd.

A I only
B II and III only
C III and IV only
D IV only
12. The following are the contraventions related to the advertisement:

I No person may take part in the publication of an advertisement which in terms


calculated to be remedy or cure for body conditions
II No person may take part in the publication of an advertisement which refer to skill or
services for any ailments
III No person may take part in the publication of an advertisement which is capable of
inducing, or which contains an invitation, whether express or implied, to, any person
referred to in the advertisement in connection with such skill or service
IV No person shall take any part in the publication of any advertisement referring to any
articles of any description as a medicine, an appliance or a remedy for the purpose of
prevention or treatment of the disease and conditions of human beings as specified in
the Schedule

A I only
B II and III only
C III and IV only
D IV only

13. The following are relevant provisions for an authorized officer who is empowered to take
action against such an advertisement:

I The Minister may authorize in writing any pharmacist to be an authorized officer


II An authorized officer making an investigation under this Act may by order in writing
require the attendance before himself of any person who from information given or
otherwise appears to be acquainted with the circumstances of the case
III He may at all reasonable times enter, search and examine such premises and may
inspect, remove and detain any advertisement, book, equipment or other article
IV Prosecutions in respect of offences under this Act or any regulation made thereunder
may be conducted by any pharmacist

A I only
B II and III only
C III and IV only
D IV only

Referring to the Medicine (Advertisement and sale) Act 1956 read the following circular before
attempting to answer QUESTIONS NO. 14 to NO. 16:

Q=max uses Tongkat Ali herbs, Ganoderma and Radix Sinensis as its main
ingredients. Packing size 350mg x 10 caps. Price: RM 800 per packing. Can solve
men’s problems such improve sex ability, sexual dysfunction. Other problems include
dizziness, sore waist, aching knee, stiff joints, insomnia, old age diseases.

Distributed by Health2u.com

14.The following body conditions of human beings from the advertisement may need approval
before the advertisement is published:

I Sex ability
II Sexual dysfunction
III Dizziness
IV Sore waist

A I only
B I, II and III only
C III and IV only
D IV only
15. The fee for an approval by Medicine Advertisement Board is

A. RM100 per advertisement medium


B. RM100 for all types of advertisement media
C. RM100 annually
D. RM100 per signage

16. The contraventions(s) found in the above advertisement is/are:

I Treatment for the impairment of sexual function


II Without approval from the Medicine Advertisement Board
III Skill or service on body ailments
IV Diagnosis of any disease

A I only
B I and II only
C I, II and III only
D III and IV only

17. The following persons shall be a Licensing Officer:

I Director General of Health


II Director of Pharmaceutical Services
III Head of Pharmacy Enforcement Division of the State
IV State Director of Medical and Health Services

A I and II only
B I, II and IV only
C II and III only
D All of the above

18. The following statement is TRUE about dispensed medicine relating to poisons:

I A licensed pharmacist or a person working under the immediate personal supervision


of a licensed pharmacist shall supply dispensed medicine
II The supply to be labeled with the word ‘POISON’ and the name of medicine
III Every medicine containing any poison shall be supplied by or under the immediate
personal supervision of a registered medical practitioner a registered practitioner of a
clinic
IV The supply to be recorded in the Poison Book

A I only
B I and III only
C II and IV only
D None of the above

19. The disease or body conditions mentioned in the publication as listed in the Schedule
is/are

I Impotency
II Insomnia
III Dizziness
IV Old age disease

A I only
B I and II only
C II only
D III and IV only

20. The following statement is TRUE of Chloramphenicol:

I The supply of Capsule Chloramphenicol for the medical treatment s of a patient shall
be recorded in the Prescription Book
II The sale of Chloramphenicol Powder B.P. by a licensed Pharmacist to a manufacturer
shall be recorded in the Poison Book.
III The retail sale of Chloramphenicol Eye Ointment by a licensed pharmacist shall be
recorded in the Prescription Book
IV The sale of 1000 ampoules of Chloramphenicol Injection by a licensed pharmacist to
a registered medical practitioner shall be recorded in the Poisons Wholesale Sales
Book

A I only
B II and IV only
C I and IV only
D I, III and IV only

21. The following statement is TRUE regarding immediate personal supervision relating
to poisons:

I A registered pharmacist or a person working under the immediate personal


supervision of a registered pharmacist shall dispense, compound or mix any poison
with any other substance
II A Group F poison may be sold or under the immediate personal supervision of a
licensed pharmacist
III Every medicine containing any poison shall be prepared by or under the immediate
personal supervision of a registered medical practitioner
IV Poison shall be sold by wholesale except by a licensed wholesaler

A I and II only
B I, II and III only
C II, III and IV only
D All of the above

22. The following statement is TRUE under the Poisons Act 1952 EXCEPT:

I False entry in record book may be fined RM 1000


II Failed to record may be fined RM 4000
III Other offences committed may be fined RM 3000
IV Employer shall be liable same penalty committed by his employee

A I only
B I, II and III only
C IV only
D None of the above

Based on the following scenario, ANSWER QUESTION NO 23 TO 24:

As a pharmacist at Kapit District Hospital, Sarawak, your daily routine includes the pharmacy
of the Outpatient Department (OPD) in the morning and Ward Pharmacy in the afternoon.
23. The following statement is TRUE for the supply of poisons to an outpatient:

I Can be supplied by medical assistant employed in the hospital in your absence


II All supply shall be via a prescription by a registered medical practitioner
III You are required to apply for Type A license
IV The container of such medicines to be labeled with the word ‘controlled medicine’

A I only
B II only
C I, II and IV only
D III only

24. The following treatment is TRUE for the supply of poison in the ward:

I Written order shall be signed by a nursing sister


II Written order shall be signed by a registered medical practitioner
III Written order shall be signed by an authorized medical assistant
IV Written order shall be signed by an authorized nursing health assistant

A I only
B I, II and III only
C I and II only
D All of the above

25. The following statement is TRUE for the storage of poison at the hospital:

I Shall be stored in a pharmaceutical department


II Shall be inspected at regular interval not exceeding 3 months
III Shall be inspected by a registered pharmacist or an appointed assistant pharmacist
IV Shall be stored in a cupboard solely reserved for poison

A I only
B I, II and III only
C I and II only
D All of the above

26. The following statement is TRUE regarding the Pharmacy Board:

I A temporarily registered pharmacist can be appointed as a member


II The secretary of the Board is appointed by the Minister
III The Director of General of Health is the president
IV The secretary of the Board is not a member

A I and II only
B II and IV only
C III and IV only
D All of the above

27. The following statement is TRUE regarding member of Pharmacy Board:

I The period of appointment of members other than ex-officio members is three years
II The Pharmacy Board consists of 18 members
III All members of the Pharmacy Board other than ex-officio member are appointed by
the Minister
IV A permanent resident of Malaysia cannot be appointed as a member of the Pharmacy
Board

A II and IV only
B II and III only
C I and III only
D All of the above

28. Which of the following statements regarding Temporary Registration are TRUE?

I The Board may temporarily register a person who is registered as pharmacist outside
Malaysia
II Only Minister can temporarily register a person who is registered as a pharmacist
outside Malaysia
III The application for temporarily registration shall be done as prescribed in the
regulations
IV A Temporarily Registered Pharmacist is deemed to be a fully registered pharmacist

A I and IV only
B II and III only
C I and III only
D All of the above

29. The following statement is TRUE about a registered body corporate EXCEPT:

I The business of the body corporate shall be under the control and management of a
superintendent who is a registered pharmacist
II The registration certificate of the pharmacist shall be conspicuously exhibited in the
premise
III The superintendent of a body corporate is not necessarily a registered pharmacist
IV If the body corporate has more than one premise, each premise shall be managed by
a separate superintendent

A I and II only
B I and III only
C II and IV only
D III and IV only

30. The following statement is TRUE regarding a registered pharmacist who is found
guilty of infamous or disgraceful conduct:

I The Board may conduct the inquiry


II The case can be mentioned in the High Court
III The Minister may conduct the inquiry
IV His name can be restored to the register after being removed

A I, II and III only


B II, III and IV only
C I and IV only
D All of the above

31. The application to postpone from commencing the public services as required under
the Registration of Pharmacists Act 1951 shall be made to the

A Human Resource Department, Ministry of Health


B Pharmacy Board
C Human Resource Unit of the Public Service Department
D Minister

32. The application to postpone the commencement in public service can be done by
submitting

A Form 10
B Form 11
C Form 12
D In writing

33. The following statement is TRUE regarding a Provisionally Registered Pharmacist


EXCEPT:

I Upon being registered, shall engage in employment as a pharmacist to the


satisfaction of the Board for a period of not less than one year
II The Provisionally Registered Pharmacist shall be deemed to be a registered
pharmacist and is allowed to apply License A
III The Board may extend for not more than 2 years the period of employment of any
Provisionally Registered Pharmacist if the Board is not satisfied with his performance
IV The Provisionally Registered Pharmacist is deemed to be a public servant during the
period of employment

A I only
B II and III only
C III and IV only
D None of the above

34. The following substances/ products are classified as dangerous drugs


A. Morphine pulv., Pethidine Injection, cannabis and heroin
B. Morphine pulv., Pethidine, cannabis and diazepam
C. Morphine pulv., dextromethorphan, cannabis and heroin
D. Morphine Injection, dextromethorphan,cannabis and heroin

35. The following / products are classified as psychotropic substances


A. Morphine Inj. (registered product), mitragynine and buprenophine
B. Flunitrazepam tablet (registered product), mitragynine and buprenophine
C. Morphine Inj., mitragynine and buprenophine
D. Cannabis, mitragynine and buprenophine

36. The supply of Syrup Methadone in government hospital for the medical treatment shall be
recorded in
A. Prescription Register for Psychotropic substances
B. Prescription Book for dispensed medicines
C. Day book for Dangerous Drugs
D. Day book and Separate Book

37. The following statements are true regarding the wholesale of registered products
containing Dihydrocodeine.
I. to be recorded in Supply Register for Psychotropic substances
II. requiring written order and written attestation
III. requiring Dangerous Drugs’ Wholesale Licence
IV. to be recorded in Separate Book for dangerous Drugs

A. I and II
B. III and IV only
C. II,III and IV
D. all of the above

38. The following statements are true regarding dangerous drugs


I. the exportation requires an export authorization
II. raw material which is supplied to be recorded in Part II Register
III. supply to patients shall be labeled as dispensed medicine for poisons
IV. disposal shall be witnessed by a Drug enforcement Officer

A. I, II and III only


B. I and II only
C. III and IV only
D. all of the above

Referring to Medicines (Advertisement and Sales) Act 1956, answer question 39 to 41


regarding the following pamphlet:

SING SHE TEO


NO.13, Jalan Langgar, Pekan Kecil, Kedah.
Specializing in acupuncture to treat;
1. Haemorrhoid
2. Hair dandruff
3. Backache
4. Fissure
5. Rheumatism
6. Rhinitis
7. Infertility

Contact us. We have 25 years of experience.


Also we use 100% traditional remedies.

Tel: Prof. Teo Tee Poo 014-59141414

39. The following statements are true


I. the advertisement refers to skill or service which is prohibited under the act
II. the advertisement refers for treatment of body conditions
III. in terms capable of inducing any person to seek his skill
IV. can beadvertised with Minister’s approval

A. I, II and III only


B. I and III only
C. III only
D. all of the above

40. The following statements are true


I. advertisement for medicine for conditions affecting human body in the pamphlet can
obtain approval
II. Medicine Advertisement Board shall not approve the advertisement for infertility
III. item number 1 to 6 in the pamphlet are not listed in the schedule
IV. can be advertised with Minister’s approval

A. II and III only


B. I and III only
C. I, II and III only
D. all of the above

41. The publication of the above advertisement is contravening the provision of


I. Section 3
II. Section 4A
III. Section 4B
IV. Section 4

A. I, II and III only


B. I only
C. II only
D. I and II only

Referring to Medicines (advertisement and Sales) Act 1956, answer question 42 regarding
the following notice:

Miracle Cure
Now available world wide
100% guarantee to cure;
1. heart problems
2. high blood pressure
3. diabetes
4. high cholesterol
5. anorexia
6. obesity.
Extract of wild herbs from Gunung Ledang. Packing of 100 capsules.
Web:
www.gunungledang.com.my on line order & courier delivery

42. Referring to Medicines (Advertisement and Sales) Act 1956, the following statements are
true regarding the above notice
I. Advertisement of condition 1,2 and 3 in the notice shall not be approved by the
Medicine Advertisement Board
II. Advertisement of conditions 4,5 and 6 in the notice may be approved by the Medicine
advertisement
III. the above notice does not require approval of medicine Advertisement Board if it
refers to naturally occurring substances
IV. Minister may give exemptions

A. I and II only
B. I, II and III only
C. I and III only
D. IV only

43. Advertisements on medical matter are allowed if


I. any person is authorized by the Minister
II. published by a private hospital after obtaining approval of Medicine Advertisement
Board
III. published by the Minister of Information
IV. published by the Malaysian Pharmaceutical Society without obtaining approval of the
Minister

A. I and II only
B. I, II and III only
C. III only
D. all of the above

44. Publication of the following advertisement is prohibited


I. medical claims of an article in a website
II. graphic on a product which is not registered with Drugs Control Authority, Ministry of
Health
III. method of using a medical instrument in traditional practice
IV. fast food
A. I only
B. II only
C. III only
D. none of the above

45. The following statements are true regarding the control of registered products
I. guidelines issued is legal
II. approval to import is issued by the Director of Pharmaceutical Services
III. indications other than that registered is allowed
IV. adding other substances into a registered product is permitted

A. I and II only
B. I and III only
C. I and IV only
D. none of the above

46. The following statements are true regarding classification


I. Potassium Permanganate 10% is a part II poison
II. Methadone tablet which is a registered product is a psychotropic substances
III. Raw material Pethidine is a dangerous drug
IV. Methadone Pulv. is a psychotropic substance

A. I, II and III only


B. I and III only
C. II and III only
D. II and IV only

47. A registered product containing pholcodeine is a


I. group C poison
II. dispensed medicine
III. psychotropic substances
IV. dangerous drug

A. I and II only
B. II and III only
C. III only
D. IV only

48. Which statements are false in relation to the Poison Board


I. the Director of Pharmaceutical services is the alternative chairman
II. in the absence of the chairman, the alternative chairman should chair the meeting
III. four members including the chairman would form a quorum
IV. the secretary is not a member of the Poison Board

A. I and II only
B. I and III only
C. I and IV only
D. all of the above

49. The powers of the Minister under the Poison Act 1952 includes
I. appoint the members of the Poison
II. appoint the secretary of the Poison Board
III. amend the Poison List
IV. issue licences

A. I, II and III only


B. II, III and IV only
C. I, III and IV only
D. all of the above
50. Poison can be imported by a
I. Type I licence holder
II. Type B licence holder as specified in the licence
III. Registered Pharmacist in Public Service for the use in the government hospital
IV. person authorized by the Minister

A. all of the above


B. I and II only
C. I and III only
D. I, II and IV only

51. The seller who sells poison by wholesale should deliver it to the purchaser
I. after he received telephone call from the purchaser
II. made entry into the wholesale book
III. after the purchaser has affixed his signature in the wholesale book or forwarded
written signed order
IV. after he received payment for the poison sold

A. II and III only


B. I and IV only
C. III and IV only
D. all of the above

52. The following are the powers of the Licensing Officer except
I. disposing the forfeited poison as ordered by the magistrate court
II. cancelling any licence previously issued
III. authorizing in writing any registered pharmacist in the public service to be Drug
Enforcement Officer
IV. issuing licences

A. I only
B. I and II only
C. I, II and III only
D. IV only

53. Labeling of dispensed medicine shall comply with the following provisions of Poisons
regulations 1952
I. Regulation 10 only
II. Regulation 12 only
III. regulation 10 and 12 only
IV. Regulations 9, 10 and 12

A. I only
B. II only
C. III only
D. IV only

54. The medicines containing poison stored in a government institution should be inspected
I. monthly
II. at regular interval not exceeding three months
III. at regular interval not exceeding six months
IV. annually

A. I only
B. II only
C. III only
D. IV only

55. The medicines containing poisons for use within a government institution could be stored
in the
I. integrated store of the hospital
II. pharmacy department
III. ward under the control of the sister in-charge of the particular ward
IV. stationary store

A. I and II only
B. I, II and III only
C. II and III only
D. all of the above

56. The following are true regarding the supply of medicine containing poison in the
government hospital to an out-patient
I. In accordance with the prescription of a registered medical practitioner
II. record of supply to be kept for a period of 2 years
III. staff nurse is allowed to issue prescriptions
IV. to be dispensed by a pharmacist only

A. I only
B. I and II only
C. I, II and III only
D. all of the above

57. The following persons are appointed under the Sale of Drugs Act 1952
I. Analyst
II. Inspector
III. Officer
IV. Drug Enforcement Officer

A. I only
B. I, II and III only
C. I and IV only
D. all of the above

58. The following statements are true;


I. the Drug Control Authority may issue 4 types of licence
II. the processing fee for a clinical trial import licence is RM 500.00
III. every licence shall be personal to the licensee named in the licence and shall not be
transferable to another person
IV. the Minister may refuse any application for a licence

A. I, II and IV only
B. I, II and III only
C. I and IV only
D. all of the above

59. Offences under the Control of Drugs and Cosmetic regulation 1984 are
I. sell any product which is not registered
II. manufacture a registered product without licence
III. sell by retail a registered product without licence
IV. a person knowing supplies false information to the Authority in connection with his
application for the registration of a product

A. I and II only
B. I, II and III only
C. I, II and III only
D. all of the above
60. The following are the responsibilities of a licensed manufacturer of a product
I. establish a quality control department under the supervision of a suitably qualified
person
II. conduct regular inspections of his manufacturing and quality control activities
III. inform the Minister of any adverse reaction arising from the use of the registered
product
IV. inform the Drug Control Authority of any adverse reaction arising from the use of the
registered product

A. I and III only


B. I and II only
C. II and IV only
D. II and III only

61. The following are the offences under the Control of Drugs and Cosmetics Regulations
1984
I. contravention of any directive by the Director of Pharmaceutical Services
II. import and sell by wholesale a registered product without licence
III. supplying false or misleading information to the Director of pharmaceutical Services
in connection with application for licence
IV. supplying false or misleading information to the Authority in connection with
application for licence

A. I and iI only
B. I, II and III only
C. II and IV only
D. all of the above

62. The following statements regarding the Committee of Inquiry formed by the Pharmacy
Board are true
I. the Director of Pharmaceutical services is the alternate chairman
II. five fully registered pharmacists can be appointed as a members
III. the Director of Health is the chairman
IV. one of the members is nominated as the chairman

A. I and II only
B. II and IV only
C. III and IV only
D. all of the above

63. The following are false


I. the pharmacy Board makes regulations for the registration of pharmacists
II. the Pharmacy Board consist of 19 members and all of them are registered pharmacist
III. all the members of the Pharmacy Board are appointed by the Minister
IV. any pharmacist who is being punished under section 18A of the Registration of
Pharmacists Act 1951 cannot appeal to the High court

A. I and IV only
B. I and III only
C. II and IV only
D. II and III only

64. The following statements about a registered body corporate are true
I. the superintendent is not necessary a registered pharmacist
II. the registration certificate of the pharmacist shall be conspicuously exhibited in the
premise
III. the business of the body corporate shall be under the control and management of a
superintendent who is a registered pharmacist
IV. if the body corporate having more than one premises, each of the premise shall be
managed by a separate superintendent
A. I and II only
B. I and III only
C. II and III only
D. III and IV only

65. The following statements are true regarding a registered pharmacist who is found guilty of
infamous or disgraceful conduct by the Board
I. his name to be removed from the register
II. his registration cannot be suspended
III. to be reprimanded
IV. his name can be restored into the register after being removed

A. I, II and III only


B. II, III and IV only
C. I, III and IV only
D. II and IV only

66. A fully registered pharmacist who fails to comply with the written notice requiring him to
assume appointment as a pharmacist in public service can be imposed by the following
actions
I. upon conviction he can be fined not more than RM 50,000.00
II. the register can revoke his registration and his name shall be deleted from the
register
III. his name will be reregistered after he pay the fine
IV. his name will be reentered in the register after an order by the Minister

A. I and II only
B. I and III only
C. I, II and IV only
D. all of the above

67. The following substances are classified as dangerous drugs


A. Morphine pulv, dextromethorphan, cannabis, heroin
B. Morphine inj, dextromethorphan, cannabis, heroin
C. Morphine pulv, pethidine,cannabis, diazepam
D. Morphine pulv, pethidine inj. (registered product), cannabis, heroin

68. The following substances are classified as psychotropic substances


A. Flunitrazepam, mitragynine, buprenorphine
B. Morphine inj. (registered product), mitragynine, buprenorphine
C. Amphetamine, mitragynine, buprenorphine
D. Cannabis, mitragynine, buprenorphine

69. The supply of Morphine tablet in a government hospital for the medical treatment shall be
recorded in
A. Day Book for Dangerous Drugs
B. Prescription Book for dispensed medicines
C. Prescription Register for Psychotropic substances
D. Poison Book for Group D Poisons

70. The following statements are true regarding the wholesale of registered products of
Pethidine Injection
I. requiring Dangerous Drugs’ Wholesale Licence
II. to be recorded in Separate Book for Dangerous Drugs
III. to be recorded in Supply Register for Psychotropic substances
IV. requiring written order and written attestation

A. I and II only
B. III and IV only
C. I, III and IV
D. All of the above
71. The following statements are true regarding dangerous drugs
I. the importation requires an import authorization
II. raw material which is imported to be recorded in Part I Register
III. supply to patients shall be labeled as dispensed medicine for poisons
IV. disposal shall be witnessed by inspector

A. I, II and III only


B. I, II and IV only
C. I, III and Iv only
D. All of the above

Referring to medicines (Advertisement and Sales) Act 1956, answer question 6 to 8 regarding
the following pamphlet:

Do you have problems such as:

U-B FINE MEDICAL CENTRE


NO.13, Jalan Pasar, Pekan Semenyih.
1. Hair loss
2. Hair dandruffs
3. Headache
4. Fainting
5. Regular feeling of tiredness, loss of energy, joint pains
6. Rhinitis
7. Infertility

Contact us. We have 20 years of experience.


Also we use 100% indigenous medicines

Tel: Wan Yik Wan Wahid 013-9131319

72. The following statements are true


I. an advertisement which is prohibited under the act
II. in terms calculated for medical treatment
III. in terms capable of inducing any person to seek his skill
IV. can be advertised with Minister’s approval

A. I and III only


B. I, II and III only
C. III only
D. All of the above

73. The following statements are true


I. advertisement for medicine for conditions affecting human body in the
pamphlet can obtain approval
II. Medicines Advertisement Board shall not approve the advertisement of item
number 7 in the pamphlet
III. item number 1 to 6 in the pamphlet are not listed in the Schedule
IV. can be advertised with Minister’s approval

A. I and III only


B. I, II and III only
C. II and III only
D. All of the above
74. The publication of the above advertisement is contravening the provision of
I. Section 3
II. Section 4
III. Section 4A
IV. Section 4B

A. I only
B. III only
C. I and III only
D. I, III and IV only

Unicity Bookstore
Now in Kajang

Solution to the heart problem, high cholesterol, diabetes, high blood pressure, stroke and
obesity in a book entitles “Natural Healing”
Stocks available. First 100 customers will be given 50% discount.

Tel: Ras 012-201919

75. Referring to Medicines (Advertisement and Sales) Act 1956, the following statements are
true regarding the above notice
I. such notice does not require approval of Medicine Advertisement Board if
circulated by the Ministry of Education
II. the book mentioned n the above notice does not require approval of Medicine
Advertisement Board if it refers to naturally occurring substances
III. the book need to be registered with Medicine Advertisement Board
IV. Minister may give exemptions

A. I, II and III only


B. I, II and IV only
C. I and II only
D. IV only

76. Advertisements of medical matters are allowed if


I. for the purpose of circulation among medical profession
II. published by a private hospital after obtaining approval of Medicine
Advertisement Board
III. published by the Ministry of Health
IV. published by the Malaysian Pharmaceutical Society after obtaining approval
of the Minister

A. I and III only


B. I, II and III only
C. III only
D. All of the above

77. Publication of the following advertisement is prohibited


I. medical claims of an article in a website
II. graphic on a product which is not registered with Drugs Control Authority,
Ministry of Health
III. method of using a medical instrument in traditional practice
IV. fast food

A. I only
B. II only
C. III only
D. None of the above
78. The following statements are true regarding the control of registered products
I. products registered by the Drug Control Authority
II. products registered by the National Pharmaceutical Control Authority
III. licence issued by the National Pharmaceutical Control Authority
IV. licence issued by the Director of Pharmaceutical Services

A. I and III only


B. I and IV only
C. II and III only
D. All of the above

79. The following statements are false regarding the control of registered products
I. guidelines issued is legal
II. approval to import is issued by the Director of Pharmaceutical Services
III. indications other than that registered is not allowed
IV. adding other substances into a registered product is prohibited

A. I and II only
B. I and III only
C. I and IV only
D. None of the above

80. The following statement(s) is (are) false regarding classification


I. Potassium Permanganate 10% is a Part II poison
II. Methadone Tab. which is a registered product is a psychotropic substance
III. Raw material Pethidine is a dangerous drug
IV. Methadone Pulv. is a psychotropic substance

81. A registered product containing opium is a


I. dangerous drug
II. psychotropic substances
III. group C poison
IV. dispensed medicine

A. all of the above


B. I and II only
C. I and III only
D. III and IV only

82. Which statement(s) is(are) true in relation to the Poison Board


I. the Director of Pharmaceutical Services is the alternative chairmen
II. in the absence of the chairman, the alternative chairman should chair the
meeting
III. four members including the chairman would form a quorum
IV. the secretary has to count the vote

A. none of the above


B. I and IV only
C. I and II only
D. III only

83. The powers of the Minister under the Poison Act 1952 includes –
I. appoint all the members of the Poison Board
II. appoint the Secretary of the Poison Board
III. amend the Poison List
IV. make regulations

A. all of the above


B. II, III and IV only
C. I, II and III only
D. I, III and IV only

84. Poisons can be imported by a


I. Type A licence holder
II. Type B licence holder as specified in the licence
III. Registered Pharmacist in Public Service for the use in the government
hospital
IV. Person authorized by the Minister

A. all of the above


B. I and II only
C. I and III only
D. I, II and IV only

85. The seller who sells poison by wholesale should deliver it to the purchaser –
I. after he received telephone call from the purchaser
II. made entry into wholesale book
III. after the purchaser has affixed his signature in the wholesale book or
forwarded written signed order
IV. after he received payment for the poison sold.

A. all of the above


B. II and III only
C. I and IV only
D. III and IV only

86. The following are the powers of the licensing Officer except
I. issuing licences
II. canceling any licence previously issued
III. authorizing in writing any registered pharmacist in the public service to be
Drug Enforcement Officer
IV. disposing the forfeited poison as ordered by the magistrate court.

A. I only
B. I and II only
C. I, II and III only
D. IV only

87. Labeling of dispensed medicine shall comply with the following provisions of Poison
Regulations 1952
I. Section 9, Regulations 9, 10 and 12.
II. Regulations 9, 10 and 12.
III. Regulations10 and 12.
IV. Regulations 12 only

A. I only
B. II only
C. III only
D. IV only

88. The medicines containing poison stored in a government institution should be inspected

21
I. regularly
II. at regular interval not exceeding three months
III. at regular interval not exceeding six months
IV. at annual department sock taking

A. I only
B. II only
C. III only
D. IV only

89. The medicines containing poison or use within a government institution could be stored in
the
I. integrated store of the hospital
II. pharmacy department
III. ward under the control of the sister in-charge of the particular ward
IV. stationary store

A. I, II and IV only
B. I and II only
C. I only
D. All of the above

90. The supply of medicine containing poisons in a government hospital to an out-patient


should be in accordance with the prescription of a
I. registered medical practitioner
II. medical assistant
III. staff nurse
IV. pharmacist

A. I only
B. I and II only
C. I, II and III only
D. All of the above

91. The following is(are) appointed by the Chief Minister under the Sale of Drugs Act 1952
I. Inspector
II. Analyst
III. Drug Enforcement Officer
IV. Officer

A. I only
B. I, II and III only
C. I and IV only
D. All of the above

92. The following statements are true except


I. the Drug Control Authority may issue 4 types of licences
II. the processing fee for a clinical trial import licence is RM 500.00
III. every licence shall be personal to the licensee named in the licence and shall
not be transferable to another person
IV. the Minister may refuse any application for a licence

A. I, II and IV only
B. I, II and III only
C. I and IV only
D. IV only

93. Offences under the Control of Drugs and Cosmetic Regulation 1984 are
I. possess for sale any product which is not registered
II. manufacture a registered product without having a valid manufacturing
licence
III. a retailer selling a registered product without having any licence
IV. a person knowing supplies false information to the Authority in connection
with his application for the registration of a product
A. I and II only
B. I, II and IV only
C. I, II and III only
D. All of the above

94. The following are the responsibilities of a licensed manufacturer of a product except
I. established a quality control department under the supervision of a suitably
qualified person
II. conduct regular inspections of his manufacturing and quality control activities
III. inform the Minister of any adverse reaction arising from the use of the
registered product
IV. ensure that all personal employed at all levels of manufacture possess
suitable qualifications required for the job.

A. I, II and IV only
B. I and II only
C. II and IV only
D. III only

95. The following are the offences under the Control of Drugs and Cosmetics Regulations
1984 except
I. contravention of directives issued by the Authority in relation to the recall of
any registered product from the market and its disposal
II. supplying any false or misleading information to the Authority in connection
with application for manufacture licence
III. supplying any false or misleading information to the Authority in connection
with application for registration of a product
IV. holding an import licence to import and sell by wholesale a registered product

A. I and II only
B. I, II and III only
C. IV only
D. All of the above

96. The following statements regarding the Committee of Inquiry formed by the Pharmacy
Board are true
I. five fully registered pharmacists can be appointed as the members
II. one of the members is nominated as the Chairman
III. the Director General of Health is the Chairman
IV. the Director of Pharmaceutical Services is the alternate Chairman

A. I and II only
B. II and IV only
C. III and IV only
D. All of the above

97. The following statements are true


I. the Pharmacy Board makes regulations for the registration of pharmacists
II. the Pharmacy Board consist of 19 members and all of them are registered
pharmacists
III. all the members of the Pharmacy Board are appointed by the Minister
IV. any pharmacist who is being punished under section 18A of the Registration
of Pharmacists Act 1951cannot appeal to the High Court

A. II and IV only
B. II and III only
C. I and III only
D. I and IV only
98. The following statements about a registered body corporate are true
I. the business of the body corporate shall be under the control and
management of superintendent who is a registered pharmacist
II. the registration certificate of the pharmacist shall be conspicuously exhibited
in the premise
III. the superintendent is not necessary a registered pharmacist
IV. if the body corporate having more than one premises, each of the premises
shall be managed by a separate superintendent

A. I and II only
B. I and III only
C. II and III only
D. III and IV only

99. The following statement is true regarding a registered pharmacist who is found guilty of
infamous or disgraceful conduct by the Board except
I. his name to be removed from the register
II. his registration to be suspended
III. to be reprimanded
IV. his name cannot be restored into the register after being removed

A. I, II and III only


B. II, III and IV only
C. I, III and IV only
D. IV only

100. A Fully Registed Pharmacist who fails to comply with the written notice requiring him to
assume appointment as a pharmacist in public service can be imposed by the following
actions except
I. upon conviction he can be fined not more than RM 50,000.00
II. the Registrar can revoke his registration and his name shall be deleted from
the register
III. his name will be reregistered after he pay the fine
IV. his name will be reentered in the register after an order by the Minister

A. I and II only
B. I and III only
C. III only
D. I, II and IV only

101. According to the Sale of Drugs Act 1952, a person commits an offence if he sells the
following drugs
I. drugs which are deleterious to Health
II. drugs which are adulterated with any prohibited substance
III. drugs which are not listed in the Schedule
IV. drugs which are for medicinal purposes

A. I only
B. I and II only
C. I, II and III only
D. All of the above

102. Under the Sales and Drugs Act 1952 and its regulation, the powers of officer and
inspector includes
I. seize drugs
II. seize products
III. detain any suspected person
IV. arrest any suspected person
A. I only
B. I and II only
C. I, II and III only
D. All of the above

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