wayground logo

Free Printable Worksheets

NEW

Font size

S
M
L
XL
Worksheets

Pharmacology Ch. 1 and 2 Consumer Safety and Drug Names

Total questions: 40

Worksheet time: 20mins

Name
Class
Date
1.

The risk of death from the use of street drugs vs prescription medications is mostly due to ________________.

a)

A lack of control over quality, purity, and strength makes street drugs dangerous

b)

The risk is the same for both sources of the some substance

c)

Street drugs are approved for use

d)

the need for prescription makes drugs hard to obtain

2.

Drug standards regulate drug manufacturers so that medications of the same name will be of the same ______________________.

a)

Strength, purity, and quality

b)

Shape, color, and taste

c)

Purity, shape, and color

d)

Quality, color, and smell

3.

The 1906 Pure Food and Drug Act includes which of the following provisions?

a)

Regulation of drugs sold in the United States and Canada

b)

Requires labeling to indicate if a medication contained a "dangerous ingredient"

c)

Regulates illicit (illegal) drugs

d)

Requires information regardidng medictions to be handed down from one practitioner to the next

4.

The Pure Food and Drug Act of 1906 was formulated ______________.

a)

To control use of drugs being abused by society

b)

As the first government attempt to establish consumer protection in the manufacture of drugs and foods.

c)

In order to make drug manufacturing profitable for the drug companies

d)

as a means to identify addicting or abused drugs

5.

Which act required that drug preparations containing morphine have a label indicating the presence of morphine?

a)

Federal Food, Drug and cosmetic Act of 1938

b)

Federal Food, Drug, and Cosmetic Act Amendment of 1965

c)

Controlled Substances Act of 1970

d)

Pure Food and Drug Act of 1906

6.

The pharmaceutical manufacturer has the ability to add additional active ingredients to a previously approved pharmaceutical products.

a)

True

b)

False

7.

Which act required that drug preparations containing morphine have a label indicating the presence of morphine?

a)

Federal Food, Drug and Cosmetic Act of 1938

b)

Federal Food, Drug, and Cosmetic Amendment of 1965

c)

Controlled Substance Act of 1970

d)

Pure Food and Drug Act of 1906

8.

Identify a provision of the Federal Food, Drug, and Cosmetic Act and its Amendments ____________________.

a)

New products are required to be approved by the Food and Drug Administration

b)

defined schedules for substances that require specific controls

c)

it set limitations on the use of prescriptions

d)

established USP

9.

The USP/NF (U.S. Pharmacopeia/National Formulary) was established to ____________.

a)

Provide a reference for all officially approved medications

b)

Legalize the manufacture of medications

c)

give the public the information needed to safely make their own drugs

d)

All of the above

10.

USP is the official abbreviation for _____________.

a)

U.S. Post Office

b)

U.S. Patrol

c)

U.S. Police

d)

U.S. Pharmacoepia

11.

Which bureau of the Department of Justice was established by the Controlled Substances Act of 1970?

a)

USP

b)

DEA

c)

FDA

d)

Nf

12.

The Controlled Substances Act of 1970 set much tighter controls on a specific group of drugs that are ______________________.

a)

at risk of being abused by society

b)

listed in the USP/NF

c)

those that contain herbal components

d)

available over the counter

13.

The Controlled Substances Act set tighter controls on ___________________.

a)

common analgesics such as Tylenol or aspirin

b)

depressants, stimulants, psychedelics, narcotics, and anabolic steroids

c)

antibiotics, diuretics, antihypertensives, and diabetic medications

d)

common cold/allergy medications

14.

Professionals needing a DEA number are ___________.

a)

registered nurses (RNs), licensed (vocational) nurses (LPN/LVNs), and certified medication assistants (CMAs)

b)

pharmacists, physicians, and veterinarians

c)

clients who have a professional license

d)

administrators of nursing care facilities, acute care hospitals, and home health care associations

15.

DEA numbers appear on the ____________.

a)

prescriber's professional license

b)

prescription for a controlled substance

c)

medication bottles that contain the controlled substance

d)

receipt for the medication

16.

Agencies/persons that are required to have a DEA number are ___________.

a)

acute care hospitals and nursing homes

b)

pharmacies, grocery stores, and convenience stores

c)

drug manufacturers and packaging facilities, pharmacists, and physicians

d)

School of nursing, medical assisting, and radiology

17.

The schedule of controlled substances that has the highest risk of abuse potential is ____________.

a)

Schedule C2

b)

Schedule C3

c)

Schedule C4

d)

Schedule C5

18.

Drugs listed in Schedule 1 of Controlled Substances ______________.

a)

are not approved for medical use in the United States

b)

may be reflled up to five times in 6 months

c)

may have prescriptions phoned in by healthcare workers

d)

have low abuse potential compared to other schedules

19.

Prescriptions of the controlled substances listed in which of these schedules MAY be called into the pharmacy by healthcare workers other than the prescriber.

a)

Schedule 1 and 2

b)

Schedules 2 through 4

c)

Schedules 4 and 5 only

d)

Schedules 1 through 3

20.

Prescriptions of the controlled substances listed in these schedules may be refilled up to five times in 6 months.

a)

Schedules 1 and 2

b)

Schedules 3 and 4

c)

Schedules 3, 4, and 5

d)

Schedules 1, 2,,3,4, and 5

21.

What is an OTC drug?

a)

Drug controlled by prescription requirement because of the danger of addiction or abuse

b)

No purchasing restrictions by the FDA

c)

Widely used reference that comes in three different formats for different users

d)

Organization working with the FDA to improve safety and prevent drug errors

22.

What is the ISMP?

a)

Legend Drug

b)

Drug controlled by prescription requirement because of the danger of addiction or abuse

c)

Organization that works with the FDA to improve medication safety and prevent drug errors

d)

Widely used reference that comes in three different formats for different users

23.

Damage to the kidneys resulting in impaired kidney function, decreased output, and renal failure

a)

Ototoxicity

b)

Photosensitivity

c)

Tall Man Lettering

d)

Nephrotoxicity

24.

Increase reaction to sunlight, with the danger of intense sunburn.

a)

Photosensitivity

b)

Ototoxicity

c)

Nephrotoxicity

d)

Tall Man Lettering

25.

Method capitalizing part of a drug name to help avoid confusing look-alike sound-alike drugs

a)

Photosensitivity

b)

Tall Man Lettering

c)

Tylenol #4

d)

Ototoxicity

26.

Drug name using a number to help differentiate it from an almost identical product

a)

Tylenol #4

b)

Photosensitivity

c)

Ototoxicity

d)

Tall Man Lettering.

27.

List of conditions for which the drug should not be given.

a)

Actions

b)

Adverse reactions

c)

Classifications

d)

Contraindications

28.

Broad subcategory to include drugs that affect the body in similar ways.

a)

Actions

b)

Cautions

c)

Classifications

d)

Contraindications

29.

Description of the cellular changes that occur as a result of the drug.

a)

Actions

b)

Adverse reactions

c)

Cautions

d)

Classifications

30.

Which name is the name by which the pharmaceutical company identifies its product, is copyrighted, and used exclusively by the company with a capitalized first letter?

a)

Generic Name

b)

Trade Name

c)

Chemical Name

d)

Official Name

31.

Which name is the exact molecular formula of the drug?

a)

generic name

b)

Trade Name

c)

Chemical name

d)

Official name

32.

The name of the drug as it appears in the official reference, the USP/NF, and which generally is the same as the generic name is _______________.

a)

generic name

b)

trade name

c)

chemical name

d)

Official name

33.

The trade name Tylenol No. 3 indicates _____________.

a)

the product contains 300 mg of acetaminophen with 15 mg of codeine

b)

the product contains 300 mg of acetaminophen with 30 mg of codeine

c)

the product contains 300 mg of acetaminophen with 60 mg of codeine

d)

None of the above

34.

Your sister is skeptical that generic drugs are as effective as brand name drugs because generics cost so much less. She asks for your opinion. What should you tell her?

a)

Generics are manufactured outside the United States, and therefore, the ingredients are unregulated.

b)

Generics and brand names are required to be identical in active and inactive ingredients.

c)

The active ingredients in generics are similar to those in brand name drugs, but are not guaranteed to be identical

d)

The active ingredients for both are identical, but fillers and other inactive ingredients may differ.

35.

Conditions or types of patients that require closer observation for specific side effects when given a drug are called __________.

a)

Adverse reactions

b)

actions

c)

cautions

d)

Interactions

36.

Conditions for which the drug should NOT be given are _______________.

a)

Adverse reactions

b)

classifications

c)

contraindications

d)

interactions

37.

An increased susceptibility to sunlight with danger of intense sunburn is ________________.

a)

ototoxicity

b)

nephrotoxicity

c)

tinnitus

d)

photosensitivity

38.

Damage to the eighth cranial nerve, resulting in impaired hearing or ringing in the ears is ______________.

a)

ototoxicity

b)

nephrotoxicity

c)

tinnitus

d)

photosensitivity

39.

Drugs controlled by prescription requirement because of the danger of addiction or abuse are _____________.

a)

OTC drugs

b)

legend drugs

c)

controlled substances

d)

None of the above

40.

Characteristics of a good drug reference for healthcare providers daily use include _____________.

i. current information, as drug information is constantly changing.

ii. concise and easily understood information

iii. information on safe and common dosing

iv. information regarding chemical structure

v. color photos

a)

All of the above

b)

None of the aobe

c)

i, ii, and iii

d)

i, ii, and v