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TEST BANK - Clayton’s Basic Pharmacology for Nurses 19th Edition Michelle Willihnganz, All Chapters 1 - 48, Newest Version

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TEST BANK - Clayton’s Basic Pharmacology for Nurses 19th Edition Michelle Willihnganz, All Chapters 1 - 48, Newest Version TEST BANK - Clayton’s Basic Pharmacology for Nurses 19th Edition Michelle Willihnganz, All Chapters 1 - 48, Newest Version

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TEST BANK FOR CLAYTON’S BASIC PHARMACOLOGY FOR
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NURSES 19TH EDITIONBY MICHELLE J. WILLIHNGANZ,
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SAMUEL L. GUREVITZ, BRUCE CLAYTON COMPLETE
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Reach me out through

, Chapter 01: Drug Definitions, Standards, and Information Sources
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Willihnganz: Clayton’s Basic Pharmacology for Nurses, 19th Edition
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MULTIPLE CHOICE h




1. Which name identifies a drug listed by the US Food
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andDrug Administration (FDA)?
h h h h


a. Brand
b. Nonproprietary
c. Official
d. Trademark
ANS: C h


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
h h h h h h h h h h h


given to a drug by its manufacturer. The nonproprietary, or
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generic, name is provided by the United States Adopted
h h h h h h h h h


Names Council.
h h




DIF: Cognitive Level: Knowledge REF: p. 9 h h h h


OBJ: 1NAT: NCLEX Client Needs Category: Safe, Effective
h h h h h h h


CareEnvironment TOP: Nursing Process Step: Assessment
h h CON: h h h h h


Patient Education
h h




2. Which source contains information specific to nutritional supplements?
h h h h h h h


a. USP Dictionary of USAN &International Drug Names
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b. Natural Medicines Comprehensive Database h h h


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


d. Drug Interaction Facts h h




ANS: C h


United States Pharmacopoeia/National Formulary contains information specific to
h h h h h h h


nutritionalsupplements. USP Dictionary of USAN & International Drug Names is a
h h h h h h h h h h h h


compilation of drugnames, pronunciation guide, and possible future FDA approved drugs; it
h h h h h h h h h h h h h


does not include nutritional supplements. Natural Medicines Comprehensive Database
h h h h h h h h h


contains
h


evidence-based information on herbal medicines and herbal combination products; it does
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notinclude information specific to nutritional supplements. Drug Interaction Facts contains
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comprehensive information on drug interaction facts; it does not include nutritional
h h h h h h h h h h h


supplements.
h




DIF: Cognitive Level: Knowledge REF: p. 4 OBJ: h h h h


3NAT: NCLEX Client Needs Category: Physiological Integrity
h h h h h h h h


TOP: Nursing Process Step: Assessment CON: Nutrition | Patient Education
h h h h h h h h




3. Which drug reference contains drug monographs that describe all drugs in a therapeutic class?
h h h h h h h h h h h h h


a. Drug Facts and Comparisons h h h




Reach me out through

,Test Bank For Clayton’s Basic Pharmacology for Nurses 19th
h h h h h h h h 3
Edition
h


b. Drug Interaction Facts h h


c. Handbook on Injectable Drugs h h h


d. Martindale—The Complete Drug Reference h h h




ANS: A h


Drug Facts and Comparisons contains drug monographs that describe all drugs in
h h h h h h h h h h h


atherapeutic class. Monographs are formatted as tables to allow comparison of
h h h h h h h h h h h h


similarproducts, 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 h h h h h h


OBJ: 3 NAT: NCLEX Client Needs Category: Physiological Integrity
hh h h h h h h h


TOP: Nursing Process Step: Assessment CON: Safety | Patient Education | Clinical Judgment
h h h h h h h h h h h




4. Which drug reference contains monographs about virtually every single-entity drug
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availablein the United States and describes therapeutic uses of drugs, including approved
h h h h h h h h h h h h h


and unapproved uses?
h h h


a. Martindale: The Complete Drug Reference h h h h


b. AHFS Drug Information h h


c. Drug Reference h


d. Drug Facts and Comparisons h h h




ANS: B h


AHFS Drug Information contains monographs about virtually every single-entity drug
h h h h h h h h h


available in the United States and describes therapeutic uses of drugs, including approved
h h h h h h h h h h h h h


andunapproved uses.
h h h




DIF: Cognitive Level: Knowledge REF: p. 4 Table 1.2 h h h h h h


OBJ: 3 NAT: NCLEX Client Needs Category: Physiological Integrity
hh h h h h h h h


TOP: Nursing Process Step: Planning
h CON: Safety | Patient Education | Clinical Judgment
h h h h h h h h h h




5. Which online drug reference makes available to healthcare providers and the public a
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standard, comprehensive, up-to-date look up and downloadable resource about medicines?
h h h h h h h h h h


a. American Drug Index h h


b. American Hospital Formulary h h


c. DailyMed
d. Drug Reference h




ANS: C h


DailyMed makes available to healthcare providers and the public a standard,
h h h h h h h h h h


comprehensive,up-to-date look up and downloadable resource about medicines. The
h h h h h h h h h h


American Drug Index isnot appropriate for patient use. The American Hospital Formulary is
h h h h h h h h h h h h h h


not appropriate for patient use. The drug reference is not appropriate for patient use.
h h h h h h h h h h h h h h




DIF: Cognitive Level: Knowledge REF: p. 3 | p. 4 OBJ: h h h h h h h


3NAT: NCLEX Client Needs Category: Physiological Integrity
h h h h h h h h


TOP: Nursing Process Step: Implementation
h h h h


CON: Safety | Patient Education | Clinical Judgment
h h h h h h h




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) h h h h h h


b. Durham Humphrey Amendment (1952) h h h

, Test Bank For Clayton’s Basic Pharmacology for Nurses 19th
h h h h h h h h 4
Edition
h


c. Controlled Substances Act (1970) h h h


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




ANS: A h


The Federal Food, Drug, and Cosmetic Act of 1938 authorized the FDA to determine the
h h h h h h h h h h h h h h


safety of all drugs before marketing. Later amendments and acts helped tighten FDA control
h h h h h h h h h h h h h h


and ensure drug safety. The Durham Humphrey Amendment defines the kinds of drugs that
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cannot be used safely without medical supervision and restricts their sale to prescription by a
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licensed practitioner. The Controlled Substances Act addresses only controlled substances
h h h h h h h h h h


andtheir categorization. The Kefauver Harris Drug Amendment ensures drug efficacy and
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greaterdrug safety. Drug manufacturers are required to prove to the FDA the effectiveness of
h h h h h h h h h h h h h h h


their products before marketing them.
h h h h h




DIF: Cognitive Level: Knowledge REF: p. 5 Table l.3 h h h h h h


OBJ: 5 hNAT: NCLEX Client Needs Category: Physiological h h h h h


IntegrityTOP: Nursing Process Step: Assessment
h h h h h h


CON: Safety | Patient Education | Evidence | Health Care Law
h h h h h h h h h h




7. Which classification does meperidine (Demerol) fall under?
h h h h h h


a. I
b. II
c. III
d. IV
ANS: B h


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


tosevere psychological and physical dependence. Schedule I drugs have high potential for
h h h h h h h h h h h h h


abuseand no recognized medical use. Schedule III drugs have some potential for abuse. Use
h h h h h h h h h h h h h h h


may lead to low to moderate physical dependence or high psychological dependence.
h h h h h h h h h h h h


Schedule IVdrugs have low potential for abuse. Use may lead to limited physical or
h h h h h h h h h h h h h h h


psychological dependence.
h h




DIF: Cognitive Level: Knowledge REF: p. 10 OBJ: h h h h


2NAT: NCLEX Client Needs Category: Safe, Effective Care
h h h h h h h h h


Environment
h


TOP: Nursing Process Step: Assessment CON: Patient Education | Addiction | Pain
h h h h h h h h h h




8. Which action would the FDA take to expedite drug development and approval for an
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outbreakof smallpox?
h h h


a. List smallpox as a health orphan disease.
h h h h h h


b. Omit the preclinical research phase. h h h h


c. Extend the clinical research phase. h h h h


d. Fast track the investigational drug.
h h h h




ANS: D h


Once the Investigational New Drug Application has been approved, the drug can receive
h h h h h h h h h h h h


highest priority within the agency, which is called fast tracking. A smallpox outbreak would
h h h h h h h h h h h h h h


become a priority concern in the world. Orphan diseases are not researched in a priority
h h h h h h h h h h h h h h h


manner. Preclinical research is not omitted. Extending any phase of the research would
h h h h h h h h h h h h h


meana longer time to develop a vaccine. The FDA must ensure that all phases of the preclinical
h h h h h h h h h h h h h h h h h h


andclinical research phase have been completed in a safe manner.
h h h h h h h h h h h




DIF: Cognitive Level: Knowledge h h REF: p. 7 hhh h OBJ: 5 h

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