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Examen

Test Bank For Clayton’s Basic Pharmacology For Nurses 18Th Edition By Willihnganz

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

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




By Michelle J. Willihnganz, Samuel L. Gurevitz, Bruce Clayton
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Complete
h

,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 and
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h Drug Administration (FDA)?
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
h h h h h h h h h h h


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 Care
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Environment TOP: Nursing Process Step: Assessment
h h CON: 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 nutritional
h h h h h h h h


supplements. USP Dictionary of USAN & International Drug Names is a compilation of drug
h h h h h h h h h h h h h h


names, pronunciation guide, and possible future FDA approved drugs; it does not include
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nutritional supplements. Natural Medicines Comprehensive Database contains
h h h h h h h


evidence-based information on herbal medicines and herbal combination products; it does not
h h h h h h h h h h h


include information specific to nutritional supplements. Drug Interaction Facts contains
h h h h h h h h h h


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: 3 h h h h h


NAT: NCLEX Client Needs Category: Physiological Integrity
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

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

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 a
h h h h h h h h h h h h


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


products, brand names, manufacturers, cost indices, and available dosage forms
h h h h h h h h h h


Online version is available.
h h h h




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


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


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




4. Which drug reference contains monographs about virtually every single-entity drug available
h h h h h h h h h h


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


unapproved uses?
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 and
h h h h h h h h h h h h h h


unapproved uses.
h h




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


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


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




5. Which online drug reference makes available to healthcare providers and the public a
h h h h h h h h h h h h


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, comprehensive,
h h h h h h h h h h h


up-to-date look up and downloadable resource about medicines. The American Drug Index is
h h h h h h h h h h h h h


not appropriate for patient use. The American Hospital Formulary is not appropriate for
h h h h h h h h h h h h h


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




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


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


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 Edition
h h h h h h h h h 4

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
h h h h h h h h h h h h h h h


licensed practitioner. The Controlled Substances Act addresses only controlled substances and
h h h h h h h h h h h


their categorization. The Kefauver Harris Drug Amendment ensures drug efficacy and greater
h h h h h h h h h h h h


drug safety. Drug manufacturers are required to prove to the FDA the effectiveness of their
h h h h h h h h h h h h h h h


products before marketing them.
h h h h




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


OBJ: h 5 NAT: NCLEX Client Needs Category: Physiological Integrity h h h h h h


TOP:
h hNursing Process Step: Assessment 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 to
h h h h h h h h h h h h h h h h h


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


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


lead to low to moderate physical dependence or high psychological dependence. Schedule IV
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drugs have low potential for abuse. Use may lead to limited physical or psychological
h h h h h h h h h h h h h h


dependence.
h




DIF: Cognitive Level: Knowledge REF: p. 10 OBJ: 2 h h h h h


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


h of smallpox?
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 mean
h h h h h h h h h h h h h h


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


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




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

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Subido en
30 de septiembre de 2024
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