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Test Bank for Pharmacotherapy Principles and Practice 6th Pharmacotherapy Principles and Practice, Sixth Edition

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Test Bank for Pharmacotherapy Principles and Practice 6th Pharmacotherapy Principles and Practice, Sixth Edition

Institution
Pharmacotherapy Principles And Practice 6th
Course
Pharmacotherapy Principles and Practice 6th











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Institution
Pharmacotherapy Principles and Practice 6th
Course
Pharmacotherapy Principles and Practice 6th

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Uploaded on
December 25, 2024
Number of pages
346
Written in
2024/2025
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Pharmacotherapy Principles and Practice 6t r r r r




h Edition Chisholm-Burns Test Bank
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CHAPTER 1. Introduction r r


1. What is the name under which a drug is listed by the U.S. Food and Drug Administration (FDA
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)?
a. Brand
b. Nonproprietary
c. Of cial r



d. Trademark
2. Which source contains information speci c to nutritional supplements?
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a. USP Dictionary of USAN & International Drug Names
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b. Natural Medicines Comprehensive Databaser r r



c. United States Pharmacopoeia/National Formulary (USP NF)
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d. Drug Interaction Facts r r



3. What is the most comprehensive reference available to research a drug interaction?
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a. Drug Facts and Comparisons r r r



b. Drug Interaction Facts
r r



c. Handbook on Injectable Drugs r r r



d. MartindaleThe Complete Drug Reference r r r



4. The physician has written an order for a drug with which the nurse is unfamiliar. Which sectio
r r r r r r r r r r r r r r r r


n of thePhysicians Desk Reference (PDR) is most helpful to get information about this drug?
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a. Manufacturers section r



b. Brand and Generic Name section
r r r r



c. Product Category section r r



d. Product Information section r r



5. Which online drug reference makes available to health care providers and the public a stand
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ard, comprehensive, up to date look up and downloadable resource about medicines?
r r r r r r r r r r r



a. American Drug Index r r



b. American Hospital Formulary r r



c. DailyMed
d. Physicians Desk Reference (PDR) r r r



6. Which legislation authorizes the FDA to determine the safety of a drug before its marketing?
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a. Federal Food, Drug, and Cosmetic Act (1938) r r r r r r



b. Durham Humphrey Amendment (1952) r r r




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