PACOP (Violet) Jurisprudence

C. Brand name

This is the proprietary name given by the manufacturer to distinguish its product from those of competitors.

A. Chemical name

B. Generic name

C. Brand name

D. Company name

E. Scientific name

A. R.A. 3720

An Act to ensure the safety and purity of foods and cosmetics, and the purity, safety, efficacy and quality of drugs and devices being made available to the public, vesting the BFAD with authority to administer and enforce the laws pertaining thereto, & for other purposes.

A. R.A. 3720

B. R.A. 6675

C. R.A. 9502

D. R.A. 9165

E. R.A. 8203

A. R.A. 9165

An Act instituting the "Comprehensive Dangerous Act of 2002", repealing R.A. 6425, as amended, providing funds therefore, and for other purposes.

A. R.A. 9165

B. R.A. 8981

C. R.A. 6675

D. R.A. 9211

E. R.A. 10354

E. R.A. 6675

An Act to promote, requires, and ensures the production of an adequate supply, distribution, use, and acceptance of drugs and medicines identified by their generic names.

A. R.A. 3720

B. R.A. 9165

C. R.A. 5921

D. R.A. 9502

E. R.A. 6675

E. R.A 9502

An act providing for cheaper and quality medicines, amending for purposes RA 8293 or the Intellectual Property code, RA 6675 or the Generic Act of 1988 and RA 5921 or the Pharmacy Law, and for other purposes.

A. R.A 9165

B. R.A 9994

C. R.A 9257

D. R.A 7876

E. R.A 9502

A. General Director of IPO

Responsible in granting a license to exploit a patented invention, even without the agreement of the patent owner, in favor of any person who has shown the capability to exploit the invention.

A. General Director of IPO

B. Director General PDEA

C. Director General of NBI

D. Director General of PDA

E. Director General of DDB

C. R.A 10918

An act regulating and modernizing the practice of pharmacy in the Philippines, repealing R.A 5921.

A. R.A 10912

B. R.A 10981

C. R.A 10918

D. R.A 10891

E. R.A 10189

B. Office of the President

The professional regulation commission (PRC) is three men commission attached to the,

A. Department of health

B. Office of the President

C. Food and Drug Administration

D. Council of Pharmaceutical Education

E. Department of the Interior and Local Government

C. Php 500.00

Indigent Senior Citizen shall be entitled to a monthly stipend amounting to to augmented the daily subsistence and other medical needs of Senior Citizens.

A. PhP 1000.00

B. PhP 2000.00

C. Php 500.00

D. PhP 300.00

E. PhP 100.00

B. Social Welfare and Development Office

The head of the OSCA shall be assisted by the City Social Welfare and Development officer, in coordination with,

A. Food and Drug Administration

B. Social Welfare and Development Office

C. Department of health

D. PhilHealth

E. City Mayor Office

B. 3

The Professional Regulation Commission is made up to ___ members.

A. 2

B. 3

C. 4

D. 5

E. 6

B. A member of the faculty of any school

The following are qualification of Regulatory Board of Pharmacy Except:

A. Be a citizen of the Philippines and resident for at least 5 years

B. A member of the faculty of any school

C. Preferably a holder of a master degree in pharmacy

D. Be a member in good standing of the APO for at least 5 years

E. None of these

A. The PRC Modernization Act of 2000

An act modernizing the Professional Regulation Commission, repealing for the purpose P.D 223, entitled " Creating Regulation Commission and Prescribing its Powers and Functions" and for the other purposes.

A. The PRC Modernization Act of 2000

B. Accredited Professional Organization Act

C. The tobacco law

D. The health Professional law

E. Act for salt Iodization nationwide

D. 18

Adult vaccine refer to cervical cancer, flu, pneumococcal, other pre-exposure prophylactic vaccines to be administered to patients aged years and above.

A. 6

B. 10

C. 15

D. 18

E. 21

A. Pharmacy Aides

Refer to persons who assist the pharmacists in the different aspect of pharmacy operation based on established standard operating procedure and processes, with very minimal degree of independence or decision making and without direct interaction with patients.

A. Pharmacy Aides

B. Pharmacy Assistants

C. Pharmacy Technicians

D. Pharmacist

E. Both A and B

D. 3 years

Chairman and the members of the Professional Regulatory Board of Pharmacy shall hold office for

A. 7 years

B. 5 years

C. 4 years

D. 3 years

E. 2 years

B. Pharmacy Assistants

Refer to persons who assist the pharmacists in the different aspect of pharmacy operation based on established standard operating procedure and processes, with very minimum degree of independence or decision making and may have supervised interaction with patient.

A. Pharmacy Aides

B. Pharmacy Assistants

C. Pharmacy Technicians

D. Pharmacist

E. Both A and B

A. R.A 9711

Bureau of Food and Drugs (BFAD) is hereby renamed the Food and Drug Administration (FDA).

A. R.A 9711

B. R.A 3720

C. R.A 9257

D. R.A 9502

E. R.A 7581

E. R.A 9711

This act shall be known as the "Food and Drug Administration Act of 2009".

A. R.A 3720

B. R.A 6675

C. R.A 7394

D. R.A 8203

E. R.A 9711

A. Referral

Refers to the process wherein a pharmacists provides consultation services and conducts preliminary assessment of symptoms and refers the patient to a physician or other health care professional.

A. Referral

B. Referral registrar

C. Prescription filling

D. Patient counseling

E. Prescription refilling

C. 50%

The senior citizen shall be entitled the grant of discount for the consumption of electricity, water and telephone by the senior citizens center and residential care/group homes that are non-stock, non-profit Domestic Corporation.

A. 20%

B. 10%

C. 50%

D. 100%

E. 5%

B. 1 year

Drug test certificates issued by accredited drug testing centers shall be valid for period from the date of issue.

A. 2 years

B. 1 year

C. 6 months

D. 3 months

E. 24 hours

A. Imprisonment of NLT 6 months and 1 day but NMT 6 years

The penalty for the possession of counterfeit drug is:

A. Imprisonment of NLT 6 months and 1 day but NMT 6 years

B. Imprisonment 6 years and 1 day but NMT 10 years

C. Imprisonment of 12 years but NMT 15 years

D. Life imprisonment to death

E. Death

A. Imprisonment of NLT 6 months and 1 day but NMT 2 years and 4 months

The penalty which shall be imposed for counterfeiting drug intended for animals.

A. Imprisonment of NLT 6 months and 1 day but NMT 2 years and 4 months

B. Imprisonment of 6 years and 1 day but NMT 10 years

C. Imprisonment of 12 years but NMT 15 years

D. Imprisonment of 4 months and 1 day but NMT 6 years

E. Life imprisonment to death

E. None of these

The following are health warning on cigarette packaged EXCEPT:

A. "GOVERNMENT WARNING: Cigarette is Addictive"

B. "GOVERNMENT WARNING: Tobacco can harm your children"

C. "GOVERNMENT WARNING: Smoking kills"

D. "GOVERNMENT WARNING: Cigarette smoking is dangerous to your health"

E. None of these

A. FDA No. 2014-067

Food and Drug Administration and PPhA Mull Plan to Authorize Community Pharmacist to Administer Vaccines.

A. FDA No. 2014-067

B. FDA No. 2014-068

C. FDA No. 2015-067

D. FDA No. 2015-068

E. FDA No. 2014-069

A. A.O 42 s.2014 DOH

Creating an Inter - Agency Committee for the Formulation and Implementation of the National Plan to Combat Antimicrobial Resistance (AMR) in the Philippines.

A. A.O 42 s.2014 DOH

B. A.O 42 s.2014 FDA

C. A.O 56 s.2014

D. A.O 64 s.2014 DOH

E. A.O 56 s.2015

A. R.A 10645

An act providing for the mandatory PHILHEALTH coverage for all SC amending for the purpose R.A 7432, as amended by R.A 9994, otherwise known "Expanded Senior Citizens Act of 2010"

A. R.A 10645

B. R.A 10354

C. R.A 10640

D. R.A 10643

E. R.A 10642

C. R.A 10640

An act to further strengthen the anti-drug campaign of the government, amending section 21 of R.A 9165, otherwise known as the "Comprehensive Dangerous Drug Acts of 2002".

A. R.A 10645

B. R.A 10354

C. R.A 10640

D. R.A 10643

E. R.A 10642

B. R.A 10354

The responsible Parenthood and Reproductive Health Act of 2012

A. R.A 10645

B. R.A 10354

C. R.A 10640

D. R.A 10643

E. R.A 10642

D. R.A 10643

An act to effectively instill health consciousness through graphic health warnings on tobacco products.

A. R.A 10645

B. R.A 10354

C. R.A 10640

D. R.A 10643

E. R.A 10642

A. DOJ

One of the members of National Coordinating and Monitoring Board of R.A 9994

A. DOJ

B. FDA

C. DILG

D. DSWD

E. DOST

B. R.A 6675

Prescription without specification on the generic name of the prescribed product is a violation of.

A. R.A 9502

B. R.A 6675

C. R.A 5921

D. R.A 8203

E. R.A 9994

B. Panic Buying

It is the abnormal phenomenon where consumers buy basic necessities and prime commodities grossly in excess of their normal requirement resulting in undue shortages of such goods to the prejudice of less privileged consumers.

A. Hoarding

B. Panic Buying

C. Profiteering

D. Cartel

E. Buffering

B. Life imprisonment to death

The penalty of cultivation of plants which are sources of prohibited drugs is:

A. 6 months rehabilitation

B. Life imprisonment to death

C. 50 years imprisonment

D. 12 years and 1 day to 20 years

E. A fine of PhP 100,000.00 to PhP 200,000.00

B. S-2

Applicable S tax for prescribers of dangerous drugs:

A. S-1

B. S-2

C. S-3

D. S-4

E. S-5-1

E. R.A 8203

The "Special Law on Counterfeit Drugs" is known as:

A. R.A 5921

B. R.A 6675

C. R.A 3720

D. R.A 7581

E. R.A 8203

B. R.A 6675

The "Generics Act" of 1988 is known as:

A. R.A 5921

B. R.A 6675

C. R.A 3720

D. R.A 7581

E. R.A 8203

A. R.A 7581

The "Price Act" is known as:

A. R.A 7581

B. R.A 7432

C. R.A 7394

D. R.A 8981

E. R.A 8344

D. 80

A certain drug is considered counterfeit if it contains less than how many percent of the active ingredient it purports to possess?

A. 10

B. 30

C. 50

D. 80

E. 100

D. 40

The principal display panel comprises percent of the total surfaces of the container.

A. 10

B. 20

C. 30

D. 40

E. 50

E. R.A 7394

The "Consumer Act of the Philippines" is known as:

A. R.A 8344

B. R.A 7432

C. R.A 7581

D. R.A 8981

E. R.A 7394

D. R.A 8293

The "Intellectual Property Code of the Philippines" is known as:

A. R.A 7581

B. R.A 7432

C. R.A 7394

D. R.A 8293

E. R.A 9502

C. R.A 9184

The "Procurement Act" is known as:

A. R.A 7876

B. R.A 8172

C. R.A 9184

D. R.A 9211

E. R.A 8423

D. R.A 8172

An "Act for salt Iodization Nationwide" or "ASIN" law is known as:

A. R.A 8293

B. R.A 9711

C. R.A 7876

D. R.A 8172

E. R.A 8344

D. R.A 8344

An act penalizing the refusal of hospital and medical clinics to administer appropriate initial medical treatment and support in emergency or serious cases, amending for the purpose Bats Pambansa bilang 702, otherwise known as "Act Prohibiting the demand of deposit or advance payments for the confinement or treatment of patient in the hospital or medical clinics in certain cases" is known as:

A. R.A 9994

B. R.A 10640

C. R.A 10645

D. R.A 8344

E. R.A 8423

B. E.O 49

Directing the mandatory use of the Philippine National Drug Formulary (PNDF) Volume 1 as the basis for Procurement of drug Products by the Government.

A. A.O 42

B. E.O 49

C. A.O 51

D. E.O 90

E. A.O 163

A. A.O 90

Amended to A.O 62 s. 1989 Re: "Rules and Regulation to implement Prescribing requirements"

A. A.O 90

B. A.O 63

C. A.O 49

D. A.O 163

E. A.O 50

A. 500g

Amount of marijuana subject to life imprisonment to death and fine ranging from PhP 500,000 to PhP 10M

A. 500g

B. 10g

C. 5g

D. 50g

E. 40g

C. A.O 42

Drug registration of Herbal and/or Traditional Drugs (Local and Import)

A. A.O 63

B. A.O 62

C. A.O 42

D. A.O 56

E. A.O 67

B. A.O 63

Revised rules and regulations to implement dispensing requirements under the Generic Act of 1988

A. A.O 55

B. A.O 63

C. A.O 62

D. A.O 64

E. A.O 67

B. 50g

Amount of Methamphetamine subject to life imprisonment to death and fine ranging from PhP 500,000 to PhP 10M.

A. 500g

B. 50g

C. 10

D. 1

E. Less than 1

E. 5

Re-application of the LTO after revocation maybe done within years.

A. 2

B. 3

C. 1

D. 4

E. 5

B. 20 working days

Duration in the conduct of examination in determining the genuineness and authenticity of suspected counterfeit drug by the Bureau is:

A. 10 working days

B. 20 working days

C. 30 working days

D. 16 working days

E. within 24 hours

C. 30 days

If the seized drug was found to be counterfeit, the business establishment must be directed for preventive closure for a period of .

A. 10 days

B. 15 days

C. 30 days

D. 45 days

E. 60 days

C. A.O 62

Revised Rules and Regulations to implement prescribing requirements under the Generics act of 1988.

A. A.O 55

B. A.O 63

C. A.O 62

D. A.O 56

E. A.O 90

B. A.O 90

This contains the amendments of A.O 62

A. A.O 55

B. A.O 90

C. A.O 42

D. A.O 64

E. A.O 67

D. 24 hours

The confiscated or seized dangerous drugs, plant sources, controlled precursor and essential chemical shall be submitted to the PDEA Forensic Laboratory for a Quantitative examination within .

A. 12 hours

B. 32 hours

C. 15 hours

D. 24 hours

E. 48 hours

D. 10g

The amount of Opium subject to life imprisonment to death and fine ranging from PhP 500,000 to PhP 10M

A. 500g

B. 50g

C. 40g

D. 10g

E. Less than 5g

D. 10g

The amount of Morphine subject to life imprisonment to death and fine ranging from PhP 500,000 to PhP 10M

A. 500g

B. 50g

C. 40g

D. 10g

E. Less than 5g

C. Referral Registry

Refers to the record book maintained by Pharmacist, listing the patients referred to different health facilities for further diagnosis:

A. Referral Book

B. Referral Journal

C. Referral Registry

D. Pharm. Book of Referral

E. Referral Compendium

E. 2

The Professional Regulatory Board of Pharmacy is composed of a Chairman and members.

A. 6

B. 5

C. 4

D. 3

E. 2

A. Board

The Professional Regulatory Board of Pharmacy created in Section 6 of R.A 10918 is called

A. Board

B. APO

C. CPD Chairman

D. Center

E. Professional Board

D. S-4

The wholesaler of Narcotics must obtain

A. S-1

B. S-2

C. S-3

D. S-4

E. S-5-C

D. S-5-D

The license for the bulk storage of specific dangerous drugs and their preparations.

A. S-5-I

B. S-5-C

C. S-5-E

D. S-5-D

E. S-5-IM

B. Impossible prescription

Unregistered imported pharmaceutical product not registered in FDA is considered .

A. Violative prescription

B. Impossible prescription

C. Erroneous prescription

D. Counterfeit Drug

E. Misbranded Drug

D. FDA

This agency monitors the presence of counterfeit drugs.

A. DOH

B. PDEA

C. PPhA

D. FDA

E. DDB

D. A.O 55

Requirements of labeling materials of Pharmaceutical products.

A. A.O 64

B. A.O 42

C. A.O 56

D. A.O 55

E. A.O 49

A. A.O 2016-0008

Revised Rules and Regulations Governing the Generic Labeling Requirements of Drug Products for Human use.

A. A.O 2016-0008

B. A.O 2016-0003

C. A.O 2015-0053

D. 2015-0008

E. 2015-0003

D. Application Form

In addition to the documentary requirements submitted during the application, the following documents shall be verified during inspection, EXCEPT:

A. Records/F-files

B. Standard Operation Procedures

C. Display information

D. Application Form

E. Relevant Display Materials

A. R.A 9994

The "Expanded Senior Citizens Act of 2010" is known as:

A. R.A 9994

B. R.A 9949

C. R.A 7432

D. R.A 9257

E. R.A 8344

B. R.A 8981

The "PRC Modernization Act" is known as:

A. R.A 7581

B. R.A 8981

C. R.A 8189

D. R.A 8423

E. R.A 7876

C. R.A 8423

The "Traditional and Alternative Medicine Act" is known as:

A. R.A 8324

B. R.A 9502

C. R.A 8423

D. R.A 9211

E. R.A 9257

A. R.A 7876

The "Senior Citizen Center Act" is known as:

A. R.A 7876

B. R.A 7687

C. R.A 7432

D. R.A 9257

E. R.A 9994

B. R.A 9502

The "Universally Accessible Cheaper and Quality Medicines Act of 2008" is known as:

A. R.A 9257

B. R.A 9502

C. R.A 8432

D. R.A 8172

E. R.A 9994

A. President of the Philippines

The Chairperson and the members of PRBP will be appointed by:

A. President of the Philippines

B. President of the APO

C. FDA Director General

D. DOH Secretary

E. PRC Chairperson

C. PRC

The PRBOP shall be under the administrative control and supervision of .

A. Office of the President

B. PPhA

C. PRC

D. FDA

E. DOH

D. No. 90 s. 1989

In response to the request of prescribing doctors to allow them to write the name of more than one drug product on the same page of a prescription form for a particular patient is A.O

A. No. 78 s. 1988

B. No. 76 s. 1989

C. No. 79 s. 1989

D. No. 90 s. 1989

E. No. 99 s. 1989

A. 1 liter

A license retail seller/handler of controlled chemical may sell acetone in a quantity not exceeding .

A. 1 liter

B. 2 liters

C. 3 liters

D. 4 liters

E. 5 liters

A. Public conveyance

Refers to mode of transportation servicing the general population such as, but not limited to, elevators, airplanes, buses, taxicabs, ships, jeepneys, light rail transits, tricycles, and similar vehicles.

A. Public conveyance

B. Public utility jeep

C. Public places

D. Public market

E. Public utility bus

D. Designated Smoking Areas

Smoking shall be absolutely prohibited in the following public places, Except:

A. Centers of youth activity such as playschools

B. Elevator and stairwells

C. Food preparation areas

D. Designated Smoking Areas

E. Public conveyance

B. 5 seconds

For radio advertisement, the warning stated after the advertisement shall be clearly and audibly voiced over in the last seconds of the advertisement, regardless of its duration.

A. 3 seconds

B. 5 seconds

C. 10 seconds

D. 15 seconds

E. 1 minute

B. DOH

Those engaged in manual salt iodization shall secure a Certificate of training from before they can be provided with a LTO.

A. FDA

B. DOH

C. DTI

D.DOST

E. DENR

B. 60

The term senior citizen shall mean any resident of the Philippines of at least years old.

A. 50

B. 60

C. 55

D. 65

E. 70

D. Over-the-Counter Drugs

The Rx symbol is required on the label of the following EXCEPT:

A. Drugs under list A

B. Drugs under list B

C. Ethical drugs

D. Over-the-Counter Drugs

E. Both A and B

E. USP/NF

Relevant reference materials needed in licensing at Retail Outlet for Non-Prescription (RONPS), Except:

A. Republic Acts

B. WHO GDP and GSP Guide

C. PNDF

D. Standard practice Guidelines

E. USP/NF

C. R.A 9165

The "Comprehensive Dangerous Drug Act of 2002" is known as :

A. R.A 9257

B. R.A 9502

C. R.A 9165

D. R.A 9994

E. R.A 9205

D. ADR Reporting

Minimum Mandatory information that shall appear in the labeling materials accompanying a drug product.

A. Product Name

B. Generic Name

C. Dosage form and strength

D. ADR Reporting

E. Storage Condition

D. To obtain information from any officer or offices of the national or local Government

The FDA shall have the following functions, powers, and duties, EXCEPT

A. To analyzed and inspect health products

B. To certify batches of antibiotics and antibiotic prescription

C. To conduct appropriate tests on all health products

D. To obtain information from any officer or offices of the national or local Government

E. To administer the effective implementation of R.A 9711

A. Property and Logistic Management Division

The Field Regulatory Operation Office of FDA shall include the following, EXCEPT:

A. Property and Logistic Management Division

B. All field offices of FDA

C. Regulatory Enforcement Units

D. Satellite Laboratories

E. Field Laboratories

A. R.A 9257

The "Expanded Senior Citizen Act of 2003" is known as:

A. R.A 9257

B. R.A 9502

C. R.A 9165

D. R.A 8981

E. R.A 7581

E. A, B and C

In R.A 9711, the meaning of "DEVICE" is:

A. Medical Devices

B. Radiation Devices

C. Health Related Devices

D. In-vitro Diagnostic Devices

E. A, B and C

D. Articles intended for use as a component of such article

Cosmetics means substance/preparations intended to be placed in, EXCEPT:

A. Contact with various external parts of the human body

B. With the Teeth

C. With the various mucous membranes of the oral cavity

D. Articles intended for use as a component of such article

E. Correcting body or keeping them in good condition

B. Suspension of LTO

A company with minor deficiencies in GMP is given the penalty of .

A. Closure of the Establishment

B. Suspension of LTO

C. Revocation of LTO

D. Temporary closure of Establishment

E. Suspension of the practice of Profession

C. Triplicate

Prescription for dangerous drug are written in

A. One copy only

B. Duplicate

C. Triplicate

D. It depends on the Physicians

E. It depends on patient request

A. Secretary of DDB

The chairman of Dangerous Drug board is the :

A. Secretary of DDB

B. Secretary of DOH

C. Secretary of DOJ

D. Director General of FDA

E. Undersecretary of PDEA

E. 10912

An act mandating and Strengthening the Continuing Professional Development for all Regulated Professions, creating Continuing Professional Development Council, and Appropriating Funds Therefore, and for other related purpose. Republic Act

A. 10640

B. 10918

C. 10990

D. 10981

E. 10912

A. P.D 223

PD which created the Professional Regulation Commission.

A. P.D 223

B. P.D 1675

C. P.D 1363

D. P.D 1926

E. P.D 881

D. Assay Procedure

A UNIT CARTON shall contain the following minimum information EXCEPT:

A. Pack Size

B. ADR Reporting Statement

C. Name and Address of marketing Authorization Letter

D. Assay Procedure

E. Storage Condition

A. FDA

Shall issue a License to Operate (LTO) to iodized salt manufacturers and salts importers/distributors upon their compliance with prescribed documentary and technical requirements.

A. FDA

B. DOH

C. DOST

D. DTI

E. TLRC