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Exam (elaborations)

Clayton’s Basic Pharmacology for Nurses (19th Edition, Michelle J. Willihnganz, Samuel L. Gurevitz & Bruce D. Clayton) Complete Test Bank

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Clayton’s Basic Pharmacology for Nurses (19th Edition, Michelle J. Willihnganz, Samuel L. Gurevitz & Bruce D. Clayton) Complete Test Bank

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Clayton’s Basic Pharmacology For Nurses 19th E
Course
Clayton’s Basic Pharmacology For Nurses 19th E











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Institution
Clayton’s Basic Pharmacology For Nurses 19th E
Course
Clayton’s Basic Pharmacology For Nurses 19th E

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Uploaded on
October 31, 2025
Number of pages
413
Written in
2025/2026
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Exam (elaborations)
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Stuvia.com - The Marketplace to Buy and Sell your Study Material
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Test Bank For Clayton’s Basic Pharmacology for Nurses 19th Edition
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By Michelle J. Willihnganz, Samuel L. Gurevitz, Bruce Clayton Com
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plete
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,Test Bank
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3
Clayton’s Material


Chapter 01: Drug Definitions, Standards, and Information Sources
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Willihnga nz: Clayton’s Basic Pharmacology for Nurses, 19th Edition
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MULTIPLE
CHOICE
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Which name identifies a drug listed by the US Food
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a nd Drug Administration (FDA)?
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Brand
Nonproprietary
Official
Trademark
ANS: C s s



The official name is the name under which a drug is listed
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by the FDA. The brand name, or trademark, is the name
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given to a drug by its manufacturer. The
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nonproprietary, o r generic, name is provided by the United
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States Adopted Names Council.
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DIF: Cognitive Level: Knowledge REF: p. 9 s s ss s s s s



OBJ: 1NAT: NCLEX Client Needs Category: Safe, Effective Ca ss ss ss ss ss ss ss ss



re Environment TOP: Nursing Process Step: Assessment
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CON:
Patient Education s s




2. Which source contains information specific to nutritional supplements?
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a. USP Dictionary of USAN &International Drug Names ss ss ss ss s ss ss



b. Natural Medicines Comprehensive Database ss ss ss



c. United States Pharmacopoeia/National Formulary (USP NF) ss ss ss ss ss



d. DrugmInteraction Facts ss




ANS: C s s



United States Pharmacopoeia/National Formulary contains information specific to nutrition
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al supplements. USP Dictionary of USAN & International Drug Names is a compilation of
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drug names, pronunciation guide, and possible future FDA approved drugs; it does not incl
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ude nutritional supplements. Natural Medicines Comprehensive Database contains
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evidence-
based information on herbal medicines and herbal combination products; it does not include
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information specific to nutritional supplements. Drug Interaction Facts contains comprehe
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nsive information on drug interaction facts; it does not include nutritional supplements.
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DIF: s s Cognitive Level: Knowledge REF: p. 4
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OBJ: 3 NAT: NCLEX Client Needs Category: Physiological Int
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egrity
TOP: s s s s Nursing Process Step: Assessment ss s s s s s s CON: s s Nutrition | Patient Education s s ss s s




3. Which drug reference contains drug monographs that describe all drugs in a therapeutic class?
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a. DrugmFacts and Comparisons ss ss

, Stuvia.com - The Marketplace to Buy and Sell your Study ss ss ss ss ss ss ss ss ss


Material

b. Drug Interaction Facts ss ss



c. Handbook on Injectable Drugs ss ss ss



d. Martindale—The Complete Drug Reference ss ss ss




ANS: A s s



Drug Facts and Comparisons contains drug monographs that describe all drugs in a
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therapeutic class. Monographs are formatted as tables to allow comparison of
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simil ar products, brand names, manufacturers, cost indices, and available dosage
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forms Online version is available.
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DIF: Cognitive Level: Knowledge REF: p. 4 Table 1.2 s s s s s s s s ss s s



OBJ: 3 NAT: NCLEX Client Needs Category: Physiological Integrity s s s s ss s s s s s s



TOP: Nursing Process Step: Assessment CON: Safety | Patient Education | Clinical Judgment
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4. Which drug reference contains monographs about virtually every single-
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entity drug available in the United States and describes therapeutic uses of drugs,
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includin g approved and unapproved uses?
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a. Martindale: The Complete Drug Reference ss ss ss ss



b. AHFS Drug Information ss ss



c. Drug Reference ss



d. Drug Facts and Comparisons ss ss ss




ANS: B s s



AHFS Drug Information contains monographs about virtually every single-
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entity drug available in the United States and describes therapeutic uses of drugs, including
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approved and unapproved uses.
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DIF: Cognitive Level: Knowledge REF: p. 4 Table 1.2 s s s s s s s s ss s s



OBJ: 3 NAT: NCLEX Client Needs Category: Physiological Integrity s s s s ss s s s s s s



TOP: Nursing Process Step: Planning CON: Safety | Patient Education | Clinical Judgment
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5. Which online drug reference makes available to healthcare providers and the public a st
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andard, comprehensive, up-to-date look up and downloadable resource about medicines?
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a. American Drug Index ss ss



b. American Hospital Formulary ss ss



c. DailyMed
d. Drug Reference ss




ANS: C s s



DailyMed makes available to healthcare providers and the public a standard, comprehensiv
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e, up-to-
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date look up and downloadable resource about medicines. The American Drug Index is not
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appropriate for patient use. The American Hospital Formulary is not appropriate for patie
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nt use. The drug reference is not appropriate for patient use.
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DIF: Cognitive Level: Knowledge REF: p. 3 | p. 4 s s s s s s s s s s s s s s



OBJ: 3 NAT: NCLEX Client Needs Category: Physiological Int
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egrity
TOP: Nursing Process Step: Implementation
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CON: Safety | Patient Education | Clinical Judgment
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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) ss ss ss s s ss s s



b. Durham Humphrey Amendment (1952) ss ss ss

, Test Bank
s s s s For Basic s s Pharma c ol og y foTrhmeNMuarsrkeestmp1la9ctehmtoEBduityi and Sell your Study ss ss ss ss
4
Clayton’s Material


c. Controlled Substances Act (1970) ss ss ss



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




ANS: A s s



The Federal Food, Drug, and Cosmetic Act of 1938 authorized the FDA to determine the
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s afety of all drugs before marketing. Later amendments and acts helped tighten FDA
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control and ensure drug safety. The Durham Humphrey Amendment defines the
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kinds of drugs th at cannot be used safely without medical supervision and restricts
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their sale to prescription by a licensed practitioner. The Controlled Substances Act addresses
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only controlled substan ces and their categorization. The Kefauver Harris Drug Amendment
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ensures drug efficacy a nd greater drug safety. Drug manufacturers are required to prove to
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the FDA the effectiven ess of their products before marketing them.
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DIF: Cognitive Level: Knowledge REF: p. 5 Table ss ss s s ss ss



l.3 OBJ: 5
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NAT: NCLEX Client Needs Category: Physiological Integrit ss ss ss ss ss ss



y TOP: Nursing Process Step: Assessment
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CON: Safety | Patient Education | Evidence | Health Care Law
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7. Which classification does meperidine (Demerol) fall under?
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a. I
b. II
c. III
d. IV
ANS: B s s



Meperidine (Demerol) is a Schedule II drug; it has a high potential for abuse and may lead ss ss ss ss ss s s ss ss ss ss ss ss ss ss s s ss



to severe psychological and physical dependence. Schedule I drugs have high potential for
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abuse and no recognized medical use. Schedule III drugs have some potential for abuse.
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U se may lead to low to moderate physical dependence or high psychological dependence.
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Sc hedule IV drugs have low potential for abuse. Use may lead to limited physical or
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psychol ogical dependence.
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DIF: Cognitive Level: Knowledge REF: p. 10
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OBJ: 2 NAT: NCLEX Client Needs Category: Safe, Effective ss s s s s ss ss ss ss ss



C are Environment
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TOP: Nursing Process Step: Assessment CON: Patient Education | Addiction | Pain
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8. Which action would the FDA take to expedite drug development and approval for an outbre
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ak of smallpox?
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a. List smallpox as a health orphan disease. ss ss ss ss ss ss



b. Omit the preclinical research phase. ss ss ss ss



c. Extend the clinical research phase. ss ss ss ss



d. Fast track the investigational drug. ss ss ss ss




ANS: D s s



Once the Investigational New Drug Application has been approved, the drug can receive h
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ighest priority within the agency, which is called fast tracking. A smallpox outbreak would
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become a priority concern in the world. Orphan diseases are not researched in a priority
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manner. Preclinical research is not omitted. Extending any phase of the research would me
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an a longer time to develop a vaccine. The FDA must ensure that all phases of the preclinic
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al and clinical research phase have been completed in a safe manner.
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DIF: Cognitive Level: Knowledge s s s s REF: p. 7 s s OBJ: 5 s s




Downloaded by: PageTurners | ss ss ss Want to earn ss ss



ss $1.236 ss





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