1. The following are the provisions of the relevant pharmacy legislations pertaining to
psychotropic substances:
A I and II only
B I, II and III only
C I, III and IV only
D All of above
A I only
B II only
C III only
D IV only
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:
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:
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):
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:
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:
Qi Sdn. Bhd
Lot 404, Bangi, Selangor
Tel: 016-4044040
11. The following are the provisions in the control of the advertisement:
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:
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:
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 I only
B I and II only
C I, II and III only
D III and IV only
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:
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
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:
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:
A I only
B I, II and III only
C IV only
D None of the above
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:
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:
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:
A I only
B I, II and III only
C I and II only
D All of the above
A I and II only
B II and IV only
C III and IV only
D All of the above
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:
31. The application to postpone from commencing the public services as required under
the Registration of Pharmacists Act 1951 shall be made to the
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
A I only
B II and III only
C III and IV only
D None of the above
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
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
A. I and II only
B. I, II and III only
C. III only
D. all 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
A. I and II only
B. II and III only
C. III only
D. IV only
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
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
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
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
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
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
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
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
Referring to medicines (Advertisement and Sales) Act 1956, answer question 6 to 8 regarding
the following pamphlet:
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.
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 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
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
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
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.
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
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
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
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
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