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Ch 3 PhT Pharmacy Law Test

Total questions: 25

Worksheet time: 13mins

Name
Class
Date
1.

The study of values or principles governing personal relationships is called:

a)

laws

b)

ethics

c)

standards

d)

etiquette

2.

An oral testimony taken by a court reporter at a location outside the courtroom, subject to the same requirements for truth as a court testimony is called:

a)

subpoena

b)

litigation

c)

deposition

d)

summons

3.

The branch of the government that is responsible for creating laws is the:

a)

executive branch

b)

judicial branch

c)

legislative branch

d)

court branch

4.

What regulatory agency is responsible for the approval of drugs, over-the-counter (OTC) and prescription labeling, and standards for drug manufacturing?

a)

Board of Pharmacy

b)

Drug Enforcement Administration (DEA)

c)

United States Pharmacopeia (USP)

d)

Food and Drug Administration (FDA)

5.

The Model State Pharmacy Practice Act (MSPPA), which can provide a greater degree of uniformity between states with regard to the practice of pharmacy, was developed by the:

a)

Board of Pharmacy

b)

National Associations of Boards of Pharmacy (NABP)

c)

Food and Drug Administration (FDA)

d)

Department of Health and Human Services

6.

Which drug is an example of a Schedule V drug that requires a prescription?

a)

Lomotil

b)

Cough syrupu with codeine (10mg/5ml)

c)

Morphine

d)

Immodium

7.

Applications for re-registration for a DEA license should be mailed approximately how many days prior to the expiration date?

a)

14 days

b)

60 days

c)

30 days

d)

120 days

8.

A pharmacist must be registered with the DEA if they:

a)

work in a pharmacy that dispenses controlled drugs

b)

own a pharmacy as a sole proprieter

c)

own a pharmacy that is incorporated

d)

never needs to be registered with the DEA

9.

Pharmacies should make a complete and accurate record of all stocks of controlled substances on hand every:

a)

month

b)

two years

c)

year

d)

three years

10.

Prescriptions for Schedule II controlled substances can be refilled:

a)

one time in six months

b)

up to five times in six months

c)

an unlimited number of times for up to a year

d)

No refills are allowed

11.

The Pure Food and Drug Act of 1906 was believed to be INADEQUATE for the following reasons EXCEPT:

a)

this act did not extend to cosmetics

b)

this act did not permit the authority to ban unsafe drugs

c)

labels were not required to identify the contents

d)

a manufacturer could not make false statements about a drug

12.

Prescriptions for Schedules III and IV controlled substances can be refilled:

a)

one time in six months

b)

an unlimited number of times for up to a year

c)

up to five times in six months

d)

No refills are allowed

13.

The official DEA form that pharmacies use to document the destruction of controlled substances is form:

a)

DEA-222

b)

DEA-106

c)

DEA-41

d)

DEA-510

14.

Patient counseling, as required by the Omnibus Budget Reconciliation Act (COBRA) of 1990, should include:

a)

the name and description of the drug

b)

the name of the manufacturer

c)

all possible side effects of the drug

d)

the pharmacokinetics of the drug

15.

Which scedule is the opiate morphine, which may result in severe psycholocial and physical dependence when abused?

a)

Schedule I

b)

Schedule II

c)

Schedule IV

d)

Schedule V

16.

Schedule IV controlled substances included drugs with:

a)

a high abuse potential and not accepted medical use

b)

a high abuse potential with a legitimate medical use

c)

the lowest abuse potential such as some narcotic drugs generally used for their antitussive properties

d)

a low abuse potential such as certain hypnotics and minor tranquilizers

17.

Who creates the standards for child-resistant packaging, as required by the Poison Prevention Packaging Act (PIPPA)?

a)

Food and Drug Administration (FDA)

b)

Drug Enforcement Agency (DEA)

c)

Consumer Product Safety Commission (CPSC)

d)

United States Pharmacopeia (USP)

18.

The agency deeply involved in the war against the human immunodeficiency virus (HIV) and acquired immunodeficiency syndrome (AIDS) is the:

a)

Food and Drug Administration (FDA)

b)

Drug Enforcement Agency (DEA)

c)

Centers for Disease Control and Prevention (CDC)

d)

Department of Health and Human Services (HHS)

19.

Which of the following amendments or acts required manufacturers to register and list their products?

a)

Medical Device Amendment

b)

Durham-Humphrey Amendment

c)

Kefauver-Harris

d)

Omnibus Budget Reconciliation Act

20.

Doctors and pharmacists are now required by the FDA to register and use a specific website in order to receive which of the follwoing medications?

a)

Ibuprofen (Motrin)

b)

Isoniazid (Isoniazid)

c)

Isotretinoin (Accutane)

d)

Isoflurane (Forane)

21.

Which of the following laws is an extension of the Patriot Act?

a)

Medicare Modernization Act

b)

Combat Methamphetamine Epidemic Act

22.

An eample of an intentional tort is:

a)

negligence

b)

libel

c)

malpractice

d)

battery

23.

Orphan drugs are used for all of the following disorders or conditions EXCEPT:

a)

snakebite

b)

peptic ulcer

c)

cystic fibrosis

d)

blepharospasm

24.

Which act prohibits the re-importation of a drug into the United States by anyone but the manufacturer?

a)

Prescription Drug Marketing Act

b)

Drug Price Competition and Patent Term Restoration Act

c)

Anabolic Steroids Control Act

d)

Orphan Drug Act

25.

The relationship between individuals within society is governed by ____ law.

a)

Civil

b)

Criminal

c)

Supreme Court

d)

State