TEST BANK FOR CLAYTON’S BASIC PHARMACOLOGY FOR NURSES 18TH EDITION BY WILLIHNGANZ

TEST BANK FOR CLAYTON’S BASIC PHARMACOLOG
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Y FOR NURSES 19TH EDITION
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,TEST BANK FOR CLAYTON’S BASIC PHARMACOLOG
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TEST BANK FOR CLAYTON’S BASIC PHARMACOLOGY FOR NURSES 19T
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H EDITION BY MICHELLE J. WILLIHNGANZ, SAMUEL L. GUREVITZ, BRUC
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E CLAYTON CHAPTER 1-48 LATEST UPDATE
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1. What is the name under which a drug is listed by the US Food and Dr
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ug Administration (FDA)?
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a. Brand
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b. Nonproprietary
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c. Official
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d. Trademark
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2. Which source contains information specific to nutritional suppleme
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nts?

a. USP Dictionary of USAN & International Drug Names
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b. Natural Medicines Comprehensive Database
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c. United States Pharmacopoeia/National Formulary (USP NF)
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,TEST BANK FOR CLAYTON’S BASIC PHARMACOLOG
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Y FOR NURSES 19TH EDITION
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d. Drug Interaction Facts
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c. United States Pharmacopoeia/National Formulary (USP NF)
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3. What is the most comprehensive reference available to research a d
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rug interaction?
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a. Drug Facts and Comparisons
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b. Drug Interaction Facts
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c. Handbook on Injectable Drugs
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d. Martindale—The Complete Drug Reference
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b. Drug Interaction Facts
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4. The physician has written an order for a drug with which the nurse is
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s unfamiliar. Which section of the Physicians' Desk Reference (PDR) is
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most helpful to get information about this drug?
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a. Manufacturer's section
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b. Brand and Generic name section
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c. Product category section
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, TEST BANK FOR CLAYTON’S BASIC PHARMACOLOG
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d. Product information section
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b. Brand and Generic name section
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5. Which online drug reference makes available to healthcare provide
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rs and the public a standard, comprehensive, up-to-
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date look up and downloadable resource about medicines?
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a. American Drug Index
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b. American Hospital Formulary
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c. DailyMed
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d. Physicians' Desk Reference (PDR)
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6. Which legislation authorizes the FDA to determine the safety of a dr
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ug before its marketing?
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a. Federal Food, Drug, and Cosmetic Act (1938)
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b. Durham Humphrey Amendment (1952)
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c. Controlled Substances Act (1970)
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d. Kefauver Harris Drug Amendment (1962)
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a. Federal Food, Drug, and Cosmetic Act (1938)
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