TEST BANK FOR CLAYTON’S BASIC PHARMACOLOGY FOR NURSES 18TH EDITION BY WILLIHNGANZz
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test bank for clayton’s basic pharmacology for nurses 18th edition by willihnganzz
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TEST BANK FOR
CLAYTON’S BASIC
PHARMACOLOGY
FOR
NURSES 18TH
EDITION
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BY WILLIHNGANZ
Downloaded by: Sophiie | abiekay12@gmail.com
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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
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TOP: Nursing Process Step: Assessment
er as
MSC: NCLEX Client Needs Category: Safe, Effective Care Environment
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2. Which source contains information specific to nutritional supplements?
a. USP Dictionary of USAN & International Drug Names
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b. Natural Medicines Comprehensive Database
c. United States Pharmacopoeia/National Formulary (USP NF)
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d. Drug Interaction Facts
ANS: C
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United States Pharmacopoeia/National Formulary contains information specific to nutritional
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supplements. USP Dictionary of USAN & International Drug Names is a compilation of drug
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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
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comprehensive information on drug interaction facts; it does not include nutritional
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supplements.
DIF: Cognitive Level: Knowledge REF: p. 2 OBJ: 4
TOP: Nursing Process Step: Assessment
is
Downloaded by: Sophiie | abiekay12@gmail.com
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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
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index in the PDR would make this section the most user friendly. Based on a physician’s
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order, manufacturer’s information and classification information would not be known. The
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Manufacturer’s section is a roster of manufacturers. The Product Category section lists
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products subdivided by therapeutic classes, such as analgesics, laxatives, oxytocics, and
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antibiotics. The Product Information section contains reprints of the package inserts for the
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major products of manufacturers.
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DIF: Cognitive Level: Comprehension REF: p. 3 OBJ: 4
TOP: Nursing Process Step: Planning
MSC: NCLEX Client Needs Category: Physiological Integrity
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aC s
5. Which online drug reference makes available to health care providers and the public a
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standard, comprehensive, up to date look up and downloadable resource about medicines?
a. American Drug Index
b. American Hospital Formulary
c. DailyMed
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d. Physicians’ Desk Reference (PDR)
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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
is
not appropriate for patient use. The American Hospital Formulary is not appropriate for
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patient use. The PDR is not appropriate for patient use.
DIF: Cognitive Level: Knowledge REF: p. 4 OBJ: 5
TOP: Nursing Process Step: Implementation
sh
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)
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