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Test Bank For Clayton’s Basic Pharmacology for Nurses 19th Edition By Michelle J. Willihnganz, Samuel L. Gurevitz, Bruce Clayton Chapter 1-48$21.49
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Test Bank For
Basic Pharmacology for Nurses
19th Edition
By
Michelle Willihnganz, Samuel L Gurevitz,
Bruce D. Clayton
,Chapter 1: Drug Definitions, Standards, and Information Sources Test
Bank
MULTIPLE CHOICE
1. What is the name under which a drug is listed by the U.S. Food and Drug Administration
(FDA)?
a. Brand
b. Nonproprietary
c. Official
d. Trademark
ANS: C
The official name is the name under which a drug is listed by the FDA. The brand name, or
trademark, is the name given to a drug by its manufacturer. The nonproprietary, or generic,
name is provided by the U.S. Adopted Names Council.
DIF: Cognitive Level: Knowledge REF: p. 1 OBJ: 2
TOP: Nursing Process Step: Assessment
MSC: NCLEX Client Needs Category: Safe, Effective Care Environment
2. Which source contains information specific to nutritional supplements?
a. USP Dictionary of USAN & International Drug Names
b. Natural Medicines Comprehensive Database
c. United States Pharmacopoeia/National Formulary (USP NF)
d. Drug Interaction Facts
ANS: C
United States Pharmacopoeia/National Formulary contains information specific to
nutritional supplements. USP Dictionary of USAN & International Drug Names is a
compilation of drug names, pronunciation guide, and possible future FDA approved drugs; it
does not include nutritional supplements. Natural Medicines Comprehensive Database
contains evidence based information on herbal medicines and herbal combination products;
it does not include information specific to nutritional supplements. Drug Interaction Facts
contains comprehensive information on drug interaction facts; it does not include nutritional
supplements.
3. What is the most comprehensive reference available to research a drug interaction?
a. Drug Facts and Comparisons
b. Drug Interaction Facts
c. Handbook on Injectable Drugs
d. Martindale—The Complete Drug Reference
ANS: B
, First published in 1983, Drug Interaction Facts is the most comprehensive book available on
drug interactions. In addition to monographs listing various aspects of drug interactions, this
information is reviewed and updated by an internationally renowned group of physicians
and pharmacists with clinical and scientific expertise.
4. The physician has written an order for a drug with which the nurse is unfamiliar. Which
section of the Physicians’ Desk Reference (PDR) is most helpful to get information about this
drug?
a. Manufacturer’s section
b. Brand and Generic Name section
c. Product Category section
d. Product Information section
ANS: B
A physician’s order would include the brand and/or generic name of the drug. The
alphabetic index in the PDR would make this section the most user friendly. Based on a
physician’s order, manufacturer’s information and classification information would not be
known. The Manufacturer’s section is a roster of manufacturers. The Product Category
section lists products subdivided by therapeutic classes, such as analgesics, laxatives,
oxytocics, and antibiotics. The Product Information section contains reprints of the package
inserts for the major products of manufacturers.
5. Which online drug reference makes available to health care providers and the public a
standard, comprehensive, up to date look up and downloadable resource about medicines?
a. American Drug Index
b. American Hospital Formulary
c. DailyMed
d. Physicians’ Desk Reference (PDR)
ANS: C
DailyMed makes available to health care providers and the public a standard,
comprehensive, up to date look up and downloadable resource about medicines. The
American Drug Index is not appropriate for patient use. The American Hospital Formulary is
not appropriate for patient use. The PDR is not appropriate for patient use.
6. Which legislation authorizes the FDA to determine the safety of a drug before its marketing?
a. Federal Food, Drug, and Cosmetic Act (1938)
b. Durham Humphrey Amendment (1952)
c. Controlled Substances Act (1970)
, d. Kefauver Harris Drug Amendment (1962)
ANS: A
The Federal Food, Drug, and Cosmetic Act of 1938 authorized the FDA to determine the
safety of all drugs before marketing. Later amendments and acts helped tighten FDA control
and ensure drug safety. The Durham Humphrey Amendment defines the kinds of drugs that
cannot be used safely without medical supervision and restricts their sale to prescription by
a licensed practitioner. The Controlled Substances Act addresses only controlled substances
and their categorization. The Kefauver Harris Drug Amendment ensures drug efficacy and
greater drug safety. Drug manufacturers are required to prove to the FDA the effectiveness
of their products before marketing them.
7. Meperidine (Demerol) is a narcotic with a high potential for physical and
psychological dependency. Under which classification does this drug fall?
a. I
b. II
c. III
d. IV
ANS: B
Meperidine (Demerol) is a Schedule II drug; it has a high potential for abuse and may lead to
severe psychological and physical dependence. Schedule I drugs have high potential for
abuse and no recognized medical use. Schedule III drugs have some potential for abuse. Use
may lead to low to moderate physical dependence or high psychological dependence.
Schedule IV drugs have low potential for abuse. Use may lead to limited physical or
psychological dependence.
DIF: Cognitive Level: Comprehension REF: p. 4 | p. 5 OBJ: 7
TOP: Nursing Process Step: Assessment
MSC: NCLEX Client Needs Category: Safe, Effective Care Environment
8. What would the FDA do to expedite drug development and approval for an
outbreak of smallpox, for which there is no known treatment? a. List
smallpox as a health orphan disease.
b. Omit the preclinical research phase.
c. Extend the clinical research phase.
d. Fast track the investigational drug.
ANS: D
Once the Investigational New Drug Application has been approved, the drug can receive
highest priority within the agency, which is called fast tracking. A smallpox outbreak would
become a priority concern in the world. Orphan diseases are not researched in a priority
manner. Preclinical research is not omitted. Extending any phase of the research would
mean a longer time to develop a vaccine. The FDA must ensure that all phases of the
preclinical and clinical research phase have been completed in a safe manner.
DIF: Cognitive Level: Knowledge REF: p. 7 OBJ: 8
TOP: Nursing Process Step: Assessment
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