1. Phenobarbitone Syrup may be dispensed, mixed and compounded by aI. Licensed pharmacist

II. Registered Medical practitioner

III. Medical Assistant in government hospitalIV. Registered nurse

A. I only

B. I and III only

C. II and III only

D. All of the above.

2. Authorization is required to import;I. Dihydrocodeine

II. Pholcodeine

III. Morphine injection

IV. Midazolam

A. I and II only

B. II and III only

C. I, II and III only

D. All the above3. The following is a requirement for the seller in wholesale sale of Thionyl Chloride

I. He is a permit holder issued by Licensing Officer

II. Written signed order shall be retained by himIII. The purchaser shall submit the permit to himIV. He shall record into the Poison Wholesale Book

A. I.II and III only

B. II and IV only

C. I, II and IV

D. All the above.

4. The following person may be authorized to investigate the offences under Poisons Act 1952 and its regulationsI. registered pharmacist in the public serviceII. customs officer

III. police officer

IV. Deputy Public ProsecutorA. I onlyB. I,II and III only

C. All of the above

D. None of the above.

5. The following statement is true regarding the prosecution in respect of offences under the Poisons Act 1952 and its regulationsI. Only Public Prosecutor may prosecute all offences

II. The Minister may authorize any registered pharmacist in the public services to conduct the prosecution

III. No prosecution shall be instituted without the sanction in writing by the Licencing OfficerIV. A Session Court shall have power to impose the full penalty

A. I and II only

B. I and III only

C. III and IV

D. IV only

6. Under the Poisons Act 1952 and its regulations, supply include; I. sell or sale

II. barterIII. direct administration

IV. offering or attempting to sellA. I and II onlyB. II and III onlyC. III and IV onlyD. None of the above

7. Entry into the Prescription Book shall be made before the supply ofI. any poisons by retail

II. Group B poison by a registered medical practitioner

III. Group C poison by a licensed pharmacist

IV. Group D poison by a licensed pharmacist

A. I and III only

B. II and III only

C. I and IV only

D. All of the above only

8. Under the Poisons Act 1952 and its regulations, the wholesale sale of Diclofenac Tablet 50mg by a licensed pharmacist, shall comply toI. Section 15

II. Regulation 8

III. Regulation 9

IV. Regulation 10

A. I only

B. I,III and IV only

C. II,III and IV only

D. All of the above

9.Under the Poisons Act 1952, all medicines containing poisons in a government institution shall be stored in the;

Ipharmaceutical department

IIgeneral store of the hospital and inspected at regular intervals

IIIwards and under the control of a person appointed for the purpose

IVany store available with air conditioner

AI only

BI and III only

CII and IV only

DAll of the above

10.The following statement is regarding offences under the Poisons Act 1952;

IKnowingly makes any false entry in such book required to be kept

IIHas in his possession an acetylating substance without authorization

IIIObstructing a Drug Enforcement Officer in the performance of his duties

IVKnowingly sell, supply, keep or store any poison without proper label

AI only

BII and III only

CII, III and IV only

DAll of the above

11. The following offence shall be punished under section 30 of the Poisons Act

1952;

ISell or supply of Buprenorphine tablet as a dispensed medicine without

label

IIDispose 1000 ampoules of expired Diazepam Injection without the presence and in accordance with the instructions of a Drug Enforcement Officer

IIIObstruct a Drug Enforcement Officer making an investigation on any

offences regarding psychotropic substancesIVPossess Acetyl Bromide and Acetyl Chloride for sale without licence

AI and II only

BI and III only

CII, III and IV only

DAll of the above

12. The Public Prosecutor may authorize in writing such persons to conduct prosecutions in respect of offences under the Poisons Act 1952;

IDrug Enforcement Officer

IIany registered pharmacist in government hospital service

IIIlicensed pharmacist

IVany health officer

AI and II only

BII only

CIII and IV only

DAll of the above

13Under the Poisons Act 1952, the Poisons List may be amended by the;

APoisons Board and by order notified in the gazette

BDirector General of Health with consent of the Poisons Board

CMinister after consultation with the Poisons Board

DMalaysian Pharmaceutical Society after consultation with the Poisons

Board

14.Under the Poisons Act 1952, the Minister may make regulations to carry out the following purposes;

Imanufacture of preparations containing poisons

IIstorage, transport and labelling of poisons

IIIcompounding, dispensing and mixing of psychotropic substances

IVpublishing the Ministry of Health Drug Formulary

AI and II only

BI, II and III only

CIII only

DAll of the above

(Note : Question 15-18, refers to Code of Conduct for Pharmacists and Bodies Corporate 2009)15.Guilty of misconduct by the following person shall be liable to disciplinary action by the Pharmacy Board;

I.A Director of a Registered Body Corporate

II. An officer of a Registered Body CorporateIII. A Provisionally Registered Pharmacist

IV. A Fully Registered Pharmacist

A.I only

B.I and II only

C.III and IV only

D.All of the above16.A pharmacist shall maintain the highest professional standard in his conduct.

The statement matches:

I. obey the laws, regulations and policies

II. report without fear any breaches of standards

III. accept inducements from suppliers

IV. drug abuse

A. I and II only

B. II only

C. III and IV only

D. All of the above

17.Professional development of a registered pharmacist can be achieved by:

I. discrediting professional integrity

II. being a party to an unauthorised research

III. aware of ethical requirements

IV. continually improving professional competence

A. I and II only

B. III only

C. IV only

D. All of the above

18.The Pharmacy Board recognizes that the profession has a duty to disseminate

information for purpose of

I. promoting his advantage

II. directing attention to his services

III. depreciating individuals

IV. advertising in an ethical manner

A. I and II only

B. III only

C. IV only

D. All of the above

19.Document relating to psychotropic substances matches the following issuing authority:

DocumentAuthority

AImport AuthorizationMinister of Health

BImport AuthorizationLicensing Officer

CPermit to purchase and useDeputy State Director (Pharmacy)

DWritten AttestationDrug Enforcement Officer

20.Written Signed Order matches the following pair of statements:

Iforwarded by purchaser before sale or supply

IIretained by supplierbefore delivery

IIIreceived by supplierIn the absence of the purchaser

IVfrom walk-in purchaserbefore payment

A. I and II only

B. I, II and III only

C. IV only

D. All of the above

21.The following type of record book for psychotropic substance matches the following person;

IPrescription Booka licensed pharmacist who sell by retail

IIPrescription Registera registered medical practitioner who supplied for his patient

IIIRegister of Psychotropic Substance, Received, Delivered or Administered a person engaged to deliver psychotropic substance

IVWholesale Sales Booka wholesaler

A. I only

B. II and III only

C. IV only

D. All of the above

22. The following is the difference between prescription of medicine containing psychotropic substance and prescription of medicine containing poisons at the government hospital;Prescription of medicine containing Psychotropic substancePrescription of medicine containing poisons

IShall be in writing Shall be hand written

IIShall state the telephone number of prescriberNo requirement of telephone number of prescriber

IIIShall supply within 90 daysNo restriction to supply within 90 days

IVShall be kept for 2 yearsNo restriction to keep prescription for 2 years

A. I only

B. II and III only

C. IV only

D. All of the above

23. Fee is required for obtaining the following document relating to psychotropic substances

I. a transit approval

II. a supporting document

IIIa permit to purchase and use

IVan import authorization

A. I only

B. II only

C. III and IV only

D. All of the above

24. Sale or supply of any product containing dangerous drug does not apply to the Dangerous Drugs Regulations 1952. The following product containing dangerous drug is controlled by the following;ProductLegal control

IMethadone SyrupAs psychotropic substances

IIPethidine InjectionAs psychotropic substances

IIIPholcodeine SyrupAs Group C Poisons

IVDiphenoxylate TabletAs psychotropic substances

A. I and II only

B. I , II and III only

C. IV only

D. All of the above

25. A wholesaler who deals with dangerous drugs may be

I. required to get wholesale licence for dangerous drugsII. issued a withdrawal of authority by the Minister

III. required to provide a written attestation

IV. issued a transit approval

A. I and II only

B. III only

C. IV only

D. All of the above

26. A pharmacist at a government hospital who deals dangerous drugs shall

I. sign all the order for supplier

II. record in Part I Register

III. supply to a patient with a prescription

IV. keep prescription for 2 years

A. I and II only

B. III only

C IV only

D. All of the above

27. The following is a requirement when a dangerous drug is obtained for the purpose of compounding or manufacturing

I. to record in Part I Register

II. to record in Part II Register

III. to keep invoices

IV. to keep other documents

A. I and II only

B. III only

C IV only

D. All of the above

28. Export authorization for dangerous drugs is issued by the A. Minister

B. Licensing Officer C Drug Control Authority

D. Customs Export Division

29. Labelling for product containing dangerous drug on storage shall have:

I. the expiry date

II. production date

III. the word POISON in four (4) languages IV. the word CONTROLLED MEDICINE

A. I and II only

B. III only

C III and IV only

D. All of the above

(Note : Question 30-34, refers to the following publication)

30. The above publication may be submitted to the Medicine Advertisement Board (MAB) and the approval to advertise such publication may be given approval by

A. Medicine Advertisement Board B. Minister

C Director of Pharmaceutical Services D. None of the above

31. The publication may be allowed without Medicine Advertisement Board (MAB) approval to advertise I. name of the pharmacy

II. contact number

III. all the tests

IV. product for mens sexual problems

A. I only

B. I and II only

C. II and III only

D. All of the above

32. The publication of advertisement may be allowed if

I. intended for professional circulation

II. the product is a registered product

III. the words sexual is deleted

IV. the advertisement is published in a website

A. I only

B. I and II only

C. II and III only

D. All of the above

33. The publication of such advertisement by a pharmacist is

I totally prohibited only for skill or services II totally prohibited only for product

III allowed due to body conditions are not listed in the Schedule IV allowed after approval by the Medicine Advertisement Board

A. I and II only

B. I ,II and III only

C. IV only

D. None of the above

34. An approval for advertisement is signed by

A. Secretary of Medicine Advertisement Board B. Licensing Officer C. Chairman of Medicine Advertisement Board

D. Minister35. The following statement is true regarding the proceeding for offences under Sales of Drug Acts 1952 and its regulations.

I. All proceedings in respect to the offences shall be taken in summary manner before Sessions Court only

II. No prosecution shall be instituted without sanction in writing of Public Prosecutor

III. The summons in any proceeding shall not be made returnable in less than 14 days from the day on which it is served

IV. All proceedings shall be made within 90 days from a day the offences convicted

A. I and III only

B. I, II and III only

C. II and IV only

D. III only

36. The following statement is TRUE regarding the President of the Pharmacy Board:

IThe Director General of Health shall be the President

IIThe President may have a casting vote IIIThe President shall be Chairman of all meetings he attends

IVIn the absence of the President from any meeting, the Director of Pharmaceutical Services shall be the Chairman

A. I and III only

B. II and IV only

C. I, II and III only

D. All of the above37. The following statement is TRUE regarding meeting of the Pharmacy Board:

I. Only the Director General of Health shall be the Chairman of all meetings

II. The Board shall meet at such places and times as the Secretary may appoint

III. Nine members including the Secretary shall form a quorum

IV. The Board may invite any person to attend any meeting

A.

I and II only

B.

II and III only

C.

III and IV only

D.

None of the above

38. The following statement is TRUE regarding members of the Pharmacy Board:

I

The period of appointment for other than ex-officio members is three

years.

IIAll members shall be citizens of Malaysia.

IIIAny appointment of any member shall be published in the Gazette.

IVThe appointment of other than ex-officio members shall be by the Minister. A. I only

B. I and II only

C. I, II and IV only

D. All of the above

39. The following statement is TRUE regarding Committee of Inquiry:IMembers are appointed by the Minister.

II

The Director of Pharmaceutical Services shall be the Chairman of a Committee.

IIIA fully registered pharmacist not in the public service may be appointed as a member.IVThe period of appointment for the members is 3 years.

A. I and II only

B. III only

C. I and IV only

D. All of the above

40. The following is a TRUE statement regarding investigation by the Committee of Inquiry on a complaint against a registered pharmacist:

I

The Secretary of the Pharmacy Board shall forward a notice stating the complaint to the affected registered pharmacist prior to the commencement of their investigation.

II

The affected registered pharmacist is required to provide to the committee a written explanation regarding the complaint within 14 days.

IIIThe committee may dismiss any complaint if the complainant is unknown.

IV

Upon completion of an investigation, the committee shall submit a report to the Director General of Health for further action.

A.

I, II and III only

B.

I, II and IV only

C.

I and III only

D.

All of the above

41. The following statement is TRUE regarding a registered body corporate:

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 premises

III. The superintendent is not necessarily a registered pharmacist

IV. If the body corporate has more than one premise, each of the premises shall be managed by a separate superintendent

A. I and II only

B. II and III only

C. I, II and IV only

D. All of the above42. The following statement is TRUE regarding application for Temporary

Registration under the Registration of Pharmacists Act 1951:I It shall be in writing to the Board.II It shall be made in writing to the Registrar.IIIIt shall be accompanied by two recent photographs of the applicant.

IVThe fee is one hundred ringgit.AI only

BII and IV only

CI, II and III only

DAll of the above

43. A person temporarily registered as a pharmacist who is not a citizen of Malaysia and working in private hospital may be appointed as

Ia member of the Pharmacy Board.IIthe Secretary of the Pharmacy Board.IIIa member of a Committee of Inquiry.

IVthe Chairman of a Committee of Inquiry.

A. I, II and III only

B. II and IV only

C. III and IV only

D. None of the above

44. The Pharmacy Board may remove the name of a registered pharmacist from the register without any inquiry if such pharmacist

I

is deceased.

II

has permanently left Malaysia.

IIIis of unsound mind.

IVcommits a breach of any restrictions and conditions under which he

is registered.

A.

I, II and III only

B.

I and IV only

C.

III only

D.

All of the above

45. Inspectors under the Registration of Pharmacists Act 1951

I. are appointed by the Minister.

II. are appointed by the Chief Minister.

III. may inspect, count or measure any drug which sale is contrary to the law.

IV. may remove and detain any document from such premises to furnish evidence of commission of an offence under this Act.A.

I and III only

B.

I and IV only

C.

II and IV only

D.

All of the above

46. The following statement is TRUE regarding certificates of registration issued under the Registration of Pharmacists Act 1951:

I. All certificates shall be signed by the Minister.II. The photograph which shall be affixed to any certificate shall be endorsed by the Secretary of the Pharmacy Board.

III. All certificates shall be signed by the Registrar.IV. The Minister may issue certificate under Section 6B(3) of the Act.A.

I and II only

B.

II and IV only

C.

III and IV only

D.

None of the above

47.The Pharmacy Board may remove the name of a registered body corporate from the register without any inquiry if

I. the registration of such body corporate has been obtained fraudulently.

II. the body corporate has ceased to carry on business of keeping, retailing, dispensing and compounding poisons, dangerous drugs or therapeutic substances.

III. any of the directors of such body corporate has been convicted of an offence under any written law relating to poisons.

IV. any of the directors has been guilty of misconduct.

A.

I and II only

B.

I, II and IV only

C.

III and IV only

D.

All of the above

48.The sale of a drug is an offence if I. it is adulteratedII. has a package of a misleading statement

III. it contains prohibited substances and nature of substances not as demanded by purchaser

IV. it contains methyl alcohol, isopropyl alcohol or denatured alcohol in external preparation

A.

I and II only

B.

I, II and III only

C.

III and IV only

D.

All of the above

49.The following person is appointed by the Chief Minister to carry out duties under the Sale of Drug Act 1952

I. Inspector

II. Officer

III. Analyst

IV. Drug Enforcement Officer

A.

I and II only

B. II and III only

C. I and IV only

D. All of the above

50. The following is an offence under the Control of Drugs and Cosmetic Regulation 1984:

I. Possession of a product which is not registered

II. Manufacture of a notified cosmetic without having manufacturing licence

III. sale by retail a registered product without licence

IV. import of a cosmetic which is not notified as part of personal luggage for personal

use for one month`s use

A. I only

B. I and II only

C. II and IV only

D. All of the above

Wan Ha Pharm

Mid-Year Promotion:

FREE Cholesterol Test, Blood Glucose Test, Blood Pressure Measurement

Bonus Product for Mens sexual problems : Refer Counter

Call : 015 505 1111

Website: HYPERLINK "http://www.wanhapharm.my" www.wanhapharm.my