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Test Bank for Pharmacotherapy Principles and Practice, 6th Edition (Chisholm-Burns, 2022), Chapter 1-102 | All Chapters

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Test Bank for Pharmacotherapy Principles and Practice, 6th Edition (Chisholm-Burns, 2022), Chapter 1-102 | All Chapters

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
April 14, 2025
Number of pages
349
Written in
2024/2025
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Pharmacotherapy Principles and Practice 6t wl wl wl wl




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


1. What is the name under which a drug is listed by the U.S. Food and Drug Administrati
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on (FDA)?wl



a. Brand
b. Nonproprietary
c. Of cial wl



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



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



b. Drug Interaction Facts wl wl



c. Handbook on Injectable Drugs wl wl wl



d. MartindaleThe Complete Drug Reference wl wl wl



4. The physician has written an order for a drug with which the nurse is unfamiliar. Whic
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h section of thePhysicians Desk Reference (PDR) is most helpful to get information about
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this drug?
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a. Manufacturers section wl



b. Brand and Generic Name sectionwl wl wl wl



c. Product Category section wl wl



d. Product Information section wl wl



5. Which online drug reference makes available to health care providers and the public
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a standard, comprehensive, up to date look up and downloadable resource about medici
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nes?
a. American Drug Index wl wl



b. American Hospital Formulary wl wl



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



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) wl wl wl wl wl wl



b. Durham Humphrey Amendment (1952) wl wl wl




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c. Controlled Substances Act (1970) wl wl wl



d. Kefauver Harris Drug Amendment (1962) wl wl wl wl




7. Meperidine (Demerol) is a narcotic with a high potential for physical and psychologic
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al dependency. Under which classi cation does this drug fall?
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a.I b wl



.II c wl



.III wl



d.IV
8. What would the FDA do to expedite drug development and approval for an outbreak of
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smallpox, for which there is no known treatment?
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a. List smallpox as a health orphan disease.
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b. Omit the preclinical research phase.
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c. Extend the clinical research phase.
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d. Fast track the investigational drug.
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9. Which statement is true about over the counter (OTC) drugs?
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a. They are not listed in the USP NF. wl wl wl wl wl wl wl



b. A prescription from a health care provider is needed.
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c. They are sold without a prescription.
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d. They are known only by their brand names.
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10. Which is the most authoritative reference for medications that are injected?
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a. Physicians Desk Reference wl wl



b. Handbook on Injectable Drugs wl wl wl



c. DailyMed
d. Handbook of Nonprescription Drugs wl wl wl



11. The nurse is administering Lomotil, a Schedule V drug. Which statement is true about th
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is drugs classi cation?
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a. Abuse potential for this drug is low. wl wl wl wl wl wl



b. Psychological dependency is likely. wl wl wl



c. There is a high potential for abuse.
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d. This drug is not a controlled substance.
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12. The nurse is transcribing new orders written for a patient with a substance abuse histo
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ry. Choose the medication ordered that has the greatest risk for abuse.
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a. Lomotil
b. Diazepam
c. Phenobarbital




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