Pharmaceutical Jurisprudence PACOP Green

c. expiration date

1.) denotes the date after which the product is not expected to retain its claim safety, efficacy and quality.

a. lot number

b. batch number

c. expiration date

d. control number

d. non operational

2.) Equipment used for manufacture, processing, testing or control must meet the ff. criteria, except;

a. non reactive

c. non absorptive

b. non additive

d. non operational

b. Bioavailability

3.) Required tests for new drugs, except;

a. Phase IV Clinical Trial

b. Bioavailability

c. Phase III

d. Phase I

c. clinical pharmacology

4.) determine the therapeutic index of drugs

a. pharmacodynamics

b. pharmacokinetics

c. clinical pharmacology

d. toxicity test

c. OSCA

5.) Government agency who issued national identification card and purchase slip booklet to senior citizen

a. BFAD

b. DILG

c. OSCA

d. DOLE

d. List A

6.) requires the representation of yellow prescription from a licensed doctor with S2 license number

a. List B

b. Rx

c. OTC

d. List A

a. EDL

7.) is a list of drug which cure the vast majority of illness, affordable and available to all persons

a. EDL

b. NDF

c. USP/NF

a. PPhA

8.) is the accredited professional pharmacy organization in the Philippines accepted by PRC

a. PPhA

b. PSHP

c. PAPPI

b. Ethics

9.) Refers to the moral principles of practice in Pharmacy

a. Jurisprudence

b. Ethics

c. Law

d. NOTA

b. Jurisprudence

10.) It is defined as a system of Laws or the Science or Philosophy of Laws

a. Pharmacy Law

b. Jurisprudence

c. RA 5921

d. Ethics

b. Food, Drug, Devices and Cosmetic Act

11.) RA 3720 is the

a. Pharmacy Law

b. Food, Drug, Devices and Cosmetic Act

c. Dangerous Drug Act

d. Senior Citizen Act

d. Dangerous Drug Act of 1972

12.) RA 6425 is the

a. Narcotic Drugs Law

b. Pharmacy Law

c. Revenue Regulation

d. Dangerous Drug Act of 1972

c. Pusher

13.) This term refers to any person who sells, administers, delivers or gives away to another any dangerous drug without any proper authority.

a. Pharmacist

b. Nurse

c. Pusher

d. Drug Agent

b. Prohibited Drugs

14.) Includes opium and its active components and derivatives such as heroin and morphine, coca leaf and its derivatives

a. Regulated Drugs

b. Prohibited Drugs

c. Both a and b

d. List B

b. narcotic drug

15.) Refers to any drug which produces insensibility, stupor, melancholy or dullness of mind with delusion

a. dangerous drug

b. narcotic drug

c. synthetic drug

d. regulated drugs

d. AOTA

16.) The only person/s authorized to issue a prescription

a. physician

b. dentist

c. veterinarian

d. AOTA

c. RA 6625

17.) An act to promote, require and ensure the production of an adequate supply, distribution, use and acceptance of drug and medicines identified by their Generic Names

a. RA 5921

b. RA 6425

c. RA 6625

d. PD 881

b. active ingredient

18.) It is the chemical component responsible for the claimed therapeutic effect of the pharmaceutical product:

a. chemical name

b. active ingredient

c. binder

d. disintegrate

c. Generic name

19.) It is the identification of drugs and medicines by their scientifically and internationally recognized active ingredient as determined by the Bureau of Food and Drugs

a. Brand name

b. label claim

c. Generic name

d. Both a and c

a. any organization or company involved in the manufacture, importation, repacking, and or distribution of drugs or medicines

20.) Drug establishments is defined as:

a. any organization or company involved in the manufacture, importation, repacking, and or distribution of drugs or medicines

b. drugstores, pharmacists and stores that sell drugs of medicines

c. Dom a and c

d. NOTA

b. brand name

21.) It is the proprietary name given by the manufacturer to distinguish its product from those of their competitors

a. generic name

b. brand name

c. common name

d. AOTA

d. AOTA

22.) The objectives of RA 5921

a. The standardization and regulation of pharmaceutical education

b. The examination for registration and graduation of schools of pharmacy in the Philippines

c. The supervision, control and regulation of the practice of pharmacy in the Philippines

d. AOTA

d. both a and b

23.) This is/ These are created for the purpose of implementing Republic Act 5921

a. Council of Pharmaceutical Education

b. Board of Pharmacy

c. Phil Pharmaceutical Association

d. both a and b

a. President of the Philippines

24.) The appointment of the Board of Pharmacy shall be approved by the:

a. President of the Philippines

b. Food and Drug Administrator

c. Commissioner of the PRC

d. AOTA

d. All of the above

25.) To be appointed member of the Board of Pharmacy, a person must be:

a. a natural born citizen of the Philippines

b. a duly registered pharmacist and has been in the practice of pharmacy for at least 10 years

c. a member of good standing of bonafide national pharmaceutical association in the Philippines

d. All of the above

a. 960 hours

26.) A complete pharmacy internship program based on RA 5921 Article III sec 18 shall consist of at least:

a. 960 hours

b. 160 hours

c. 480 hours

d. 980 hours

b. 75%

27.) In order to pass the board examination, a candidate must obtain a general average of

a. 100%

b. 75%

c. 50%

d. 80%

c. twice a year

28.) Examination for registration to practice pharmacy in the Philippines shall be given:

a. once a year

b. thrice a year

c. twice a year

d. 5x a year

d. AOTA

29.) In order for somebody to practice pharmacy in the Philippines, he must be:

a. at least 21 years old

b. has satisfactorily passed the examination given by the board of pharmacy

c. holder of a valid certificate of registration duly issued to him by the Board of Pharmacy

d. AOTA

a. it bears or contains any poisonous substance which may render it injurious to health

30.) A food shall be deemed adulterated if:

a. it bears or contains any poisonous substance which may render it injurious to health

b. its labeling is false or misleading

c. both a and b

d. none of the above

b. its labeling is false or misleading

31.) A food shall be deemed misbranded:

a. it bears or contains any poisonous substance which may render it injurious to health

b. its labeling is false or misleading

c. both a and b

d. none of the above

d. all of the above

32.) In R.A. no. 3720 Section 10, food means:

a. articles used for food or drink for man

b. chewing gum

c. articles used for components of any such article

d. all of the above

d. all of the above

33.) In R.A. no. 3720 Section 10, drug means:

a. any article recognized in the official Pharmacopeia and National Formulary

b. articles intended for use in the diagnosis, cure and mitigation, treatment or prevention of diseases in man and other animals

c. articles intended for any function of the body of man

d. all of the above

a. strength

34.) It is the concentration of known active drug substance in the formulation:

a. strength

b. percentage

c. batch size

d. AOTA

c. both a and b

35.) In tablets, this/these test/s is/are usually performed:

a. weight variation, content uniformity, hardness

b. disintegration and dissolution for the active ingredients

c. both a and b

d. NOTA

a. viscometer

36.) In the preparation of liquid or suspension one of the choices below is necessary:

a. viscometer

b. moisture balance

c. particle counter

d. leaker test

a. tried and tested

37.) It is a drug which has been used for at least five years, involving at least 5,000 patients

a. tried and tested

b. established drug

c. drug for general

d. investigational drug

b. established drug

38.) It is a drug the safety and efficacy of which has been demonstrated through long years of general use and can be found in current USP-NF and other internationally recognized Pharmacopeia:

a. tried and tested

b. established drug

c. drug for general use

d. investigational drug

d. AOTA

39.) The source or circumstances of drug production is/are:

a. imported as finished

b. locally manufactured from imported materials

c. locally manufactured from local materials

d. AOTA

a. red colored label

40.) Products for external use bears:

a. red colored label

b. white colored label

c. any color as long as the statement "for external use only" is indicated

d. green colored label

а. 10%

41.) Test for alcohol content should not be more than

а. 10%

b. 20%

c. 75%

d. 40%

d. AOTA

42.) All information required to appear on the label must be:

a. written in English or Filipino

b. clearly and prominently displayed

c. readable with normal vision without straining, the color contrast, the position and sparing of the information must be taken into consideration in complying with labeling requirements

d. AOTA

d. AOTA

43.) In the current good manufacturing practice, we usually consider the;

a. building

b. personnel

c. equipment

d. AOTA

c. 20%

44.) A senior citizen who purchase his medicine for his personal needs is entitled to a minimum discount of:

a. 10%

b. 30%

c. 20%

d. 15%

c. Dangerous Drug prescriptions are issued by the Board of Pharmacy

45.) The following statements are true, except;

a. Prescriber of Dangerous Drugs should have S2 license issued by the Dangerous Drug Board

b. Dangerous Drug prescriptions are accomplished in triplicate

c. Dangerous Drug prescriptions are issued by the Board of Pharmacy

d. The original copy of the Dangerous Drug Prescription should be kept by the pharmacist

d. Absence of pharmacist on three (3) inspections by BAD inspector

46.) License to operate (LTO)of a drugstore can be suspended except

a. Refusal to allow entry of BAD inspector during business hours

b. Failure to properly record and keep of all prescriptions received in the last two years

c. Failure to produce invoices and receipts together with lot numbers, expiration dates for the drug on stocks

d. Absence of pharmacist on three (3) inspections by BAD inspector

d. Violative Rx should not be filled by pharmacist, Rx kept by pharmacist and reported to DOH

47.) The ff. statements are incorrect, except;

a. Erroneous prescriptions should not be filled by pharmacist, Rx kept and reported to DOH

b. Violative Rx could be filled, x kept and reported to DOH

c. Impossible Rx could be filled, Rx kept and reported to DOH

d. Violative Rx should not be filled by pharmacist, Rx kept by pharmacist and reported to DOH

d. failure to return the Rx to the patient

48.) The ff. are violations under the Generic Act which a pharmacist may commit except:

a. imposing a particular brand on the buyer

b. failure to make accessible the required up-to-date information on drug products to the buying public

c. failure to report to the nearest DOH

d. failure to return the Rx to the patient

a. minimum of 50 sq. m. floor area with concrete, tile of wooden flooring

49.) Requirement for drug store except:

a. minimum of 50 sq. m. floor area with concrete, tile of wooden flooring

b. adequate water supply

c. reference books and documents such as USP

d. prescription book

a. drug manufacturers

50.) Product standardization is the responsibility of:

a. drug manufacturers

b. retailers

c. whole

d. importers

b. RA 3720

51.) An act to ensure the safety and purity of foods, drugs, devices and cosmetics in the country

a. RA 5921

b. RA 3720

c. RA 6425

d. RA 953

b. Bureau of Food and Drugs

52.) Drug product registration is regulated by:

a. Secretary of Health

b. Bureau of Food and Drugs

c. Multinational Companies

d. Local companies

d. indications

53.) Principal display label must contain the following, except:

a. pharmacologic category

b. dosage form and strength

c. net content

d. indications

c. suspension of license to operate

54.) Refusal to allow entry of BAD inspectors is penalized by:

a. revocation of certificate of registration

b. temporary closure

c. suspension of license to operate

d. revocation of license to operate

b. Regulation Division II

55.) That division in BAD which is in charge of the inspection of manufacturers of foods, drugs and cosmetics

a. Regulation Division I

b. Regulation Division II

c. Product Services

d. Legal Division

a. DOH

56.) BAD is a regulatory agency of the national government under

a. DOH

b. DDB

c. Office of the President

d. Professional Regulation Commission

c. adulteration

57.) The presence of foreign matter inside the contents of a bottled syrup is a case of

a. misbranding

b. adultery

c. adulteration

d. mislabeling

b. two vears

58.) All prescriptions dispensed in the drugstores shall be kept on file for:

a. one vear

b. two vears

c. three years

d. five years

c. impossible prescription

59.) When only the generic name is written but is not legible is a case of;

a. violative prescription

b. erroneous prescription

c. impossible prescription

d. NOTA

b. erroneous prescription

60.) Where the brand name is not in parenthesis is a case of;

a. violative prescription

b. erroneous prescription

c. impossible prescription

d. NOTA

d. keeping of list of patients who purchase drug in the drugstore

61.) One of these is not a requirement for opening a drugstore

a. full time registered pharmacist

b. keeping of record books duly registered with BAD

c. keeping of invoice indicating lot number or batch number of the manufacturer's stock

d. keeping of list of patients who purchase drug in the drugstore

b. DDB

62.) Prescription forms for dangerous drugs are issued by:

a. BFAD

b. DDB

c. BIR

d. PRC

b. triplicate

63.) Prescription for dangerous drugs are written in:

a. duplicate

b. triplicate

c. one copy

d. any of the above

a. PRC

64.) The Board of Pharmacy is under the supervision of:

a. PRC

b. Civil Service Commission

c. CHED

d. DOH

a. one year

65.) The pharmacist should keep the copy of the original narcotic prescription for the period of

a. one year

b. two years

c. five years

d. four years

d. BFAD

66.) A permit to operate a retail drugstore is issued by;

a. DDB

b. BIR

c. Board of Pharmacy

d. BFAD

c. PRC

67.) Government office where the professional register and where license is issued:

a. Bureau of Domestic Trade

b. Bureau of Food and Drug

c. PRC

d. BIR

d. AOTA

68.) A candidate for Board of Examination:

a. shall be a Filipino citizen of the Philippines

b. must be of good moral character

c. must have completed 960 hours of internship

d. AOTA

c. honesty

69.) Grounds for reprimand, suspension or revocation of registration certificate, except:

a. insanity

b. immorality

c. honesty

b. antibiotics

70.) Drugs which require batch certification before it can be released to the market:

a. anesthetics

b. antibiotics

c. antineoplastics

b. month and year

71.) The expiration date of the drug shall be expressed in terms of

a. day and year

b. month and year

c. month and day

b. Vignette representing skull and bones

72.) Poisonous preparation must bear

a. Rx symbol

b. Vignette representing skull and bones

c. external use only

e. AOTA

73.) Counterfeit drugs refers to:

a. product with correct ingredients but not in the amount provided

b. product with wrong ingredients

c. product with insufficient quantity of active ingredients

d. drugs which is fraudently mislabeled

e. AOTA

d. drugs which is fraudently mislabeled

74.) Parties liable for violation of RA 8203 are, except:

a. manufacturer

b. pharmacist

c. processor of counterfeit drugs

d. drugs which is fraudently mislabeled

e. AOTA

b. FDRO's

75.) Monitors the presence of counterfeit drugs

a. DOH

b. FDRO's

c. CHED

d. DDB

d. DDB

76.) Pharmacists are required to report record of sales of dangerous drugs twice a year to the

a. BFAD

b. DOH

c. Municipal Health Officer

d. DDB

d. illegal importation, distribution, manufacture

77.) Which of the violative acts will warrant closure of establishment

a. failure to record sales and purchases for dangerous drug

b. loss of Rx form for dangerous drug

c. failure to comply with filling of prescription for dangerous drug

d. illegal importation, distribution, manufacture

b. Dangerous Drug

78.) Which of the following drug preparation cannot be distributed as samples

a. OTC

b. Dangerous Drug

c. Rx Drug

d. AOTA

b. one week supply

79.) Supplies/medicines to be given to senior citizen should not exceed;

a. one day supply

b. one week supply

c. one month supply

d. one year supply

d. AOTA

80.) The following must be presented by senior citizens when buying drugs;

a. prescription

b. Purchase slip booklet

c. OSCA identification card

d. AOTA

c. liaison officer

81.) BFAD requires all manufacturing company to designate a person who will transact officially with BFAD

a. medical director

b. product manager

c. liaison officer

d. quality control manager

c. while the outlet is open for business

82.) Pharmacists are requested by law to be in drugstore

a. for 8 hours

b. in the morning only

c. while the outlet is open for business

d. when there is BAD inspector

a. Republic Act Book

83.) The following are record book except;

a. Republic Act Book

b. Dangerous Drug Book

c. Poison Book

d. Prescription Book

b. BFAD

84.) The minimum requirement necessary for the opening of retail drugstore must be in accordance with the rules and

regulations of:

a. DDB

b. BFAD

c. Board of Pharmacy

d. DOH

a. Pharmacy Law

85.) Sale of physician sample is a prohibited act under the:

a. Pharmacy Law

b. Generics law

c. Foods, Drugs, Devices, and Cosmetics law

d. Dangerous Drug Act

b. EO 174

86.) The latest amendments to RA 5921 is

a. EO 175

b. EO 174

c. RA 3720

d. PD L916

b. Drug Outlet

87.) Drugstore, Pharmacy and other business establishment which sell drug or medicine is known as:

a. Drug Establishment

b. Drug Outlet

c. Drug Trader

d. Drug Manufacturers

c. President of the Phil

88.) Who has sole authority to remove a member of the Board of Pharmacy,, for cause provided in the laws?

a. Chairman, PRC

b. Chairman, BOP

c. President of the Phil

d. President of Prof. Org.

a. 30 davs

89.) The decision of the Board of Pharmacy in administrative cases involving a pharmacist becomes final and executory

after the lapse of:

a. 30 davs

b. 15 days

c. 60 days

d. 90 days from notice to respondent

a. PRC

90.) The Board of Pharmacy is under the supervision of:

a. PRC

b. Civil Service Commission

c. CHED

d. DOH

b. 10 vears

91.) To be appointed as member of the Board of Pharmacy, a pharmacist must have practiced for at least;

a. 5 years

b. 10 vears

c. 15 years

d. 2 years

c. Board of Pharmacy

92.) Detailmen are requested to register with the:

a. Board of Medicine

b.BFAD

c. Board of Pharmacy

d. PRC

a. examine applicants for the practice of pharmacy

93.) One of the functions of the Board of Pharmacy

a. examine applicants for the practice of pharmacy

b. to authorize opening of drugstore

c. to collect samples of drugs, medicines and cosmetics

d. to accredit colleges of pharmacy

d. 1969

94.) RA 5921 was approved in:

a. 1965

b. 1970

c. 1960

d. 1969

b. Ethics

95.) Refers to the moral principles of the practice of pharmacy:

a. Jurisprudence

b. Ethics

c. Law

d. both a and c

b. 3 yrs.

96.) How many years shall the chairman of the Board of Pharmacy hold office after appointment?

a. 2 yrs

b. 3 yrs.

c. 4 yrs

d. 1 yr

d. Absence of pharmacist on three (3) inspections by BAD inspector

97.) License to operate (LTO) a drugstore can be suspended EXCEPT

a. Refusal to allow entry of BAD inspector during business hours

b. Failure to properly record and keep file of all prescriptions received in the last two years

c. Failure to produce invoices and receipts together with lot numbers, expiration dates for the drug stocks

d. Absence of pharmacist on three (3) inspections by BAD inspector

c. a fine of not less than P1000 but not exceeding P4000 or an imprisonment of not less than 6 mos and one day but not more than 4 yrs.

98.) The penalty for any person who falsely display within the establishment the certificate of registration of a pharmacist not actually or regularly employed is:

a. a fine of more than P1000 or imprisonment of 6 mos

b. a fine of not less than P1000 but not exceeding P4000 or an imprisonment of not less than 4 yrs

c. a fine of not less than P1000 but not exceeding P4000 or an imprisonment of not less than 6 mos and one day but not more than 4 yrs.

b. brand name

99.) It is the proprietary name given by the manufacturer to distinguish its product from those of their competitors

a. generic name

b. brand name

c. common name

d. AOTA

c. minimum penalty

100.) Penalty imposed when the counterfeit drugs are not life saving drugs and the volume of the drug involved is not more

than one million

a. maximum penalty

b. medium penalty

c. minimum penalty

d. revocation of LTO