Test Bank For Clayton’s Basic Pharmacology for Nurses 19th EditionB
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y Michelle J. Willihnganz, Samuel L. Gurevitz, Bruce Clayton Compl
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ete
,Chapter 01: Drug Definitions, Standards, and Information Sources Willihnga
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nz: Clayton’s Basic Pharmacology for Nurses, 19th Edition
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MULTIPLE CHOICE wl
1. Which name identifies a drug listed by the US Food a
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ndDrug Administration (FDA)?
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a. Brand
b. Nonproprietary
c. Official
d. Trademark
ANS: C wl
The official name is the name under which a drug is liste
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d by the FDA. The brand name, or trademark, is the name
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given to a drug by its manufacturer. The nonproprietary,
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or generic, name is provided by the United States Adopted
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Names Council.
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DIF: Cognitive Level: Knowledge REF: p. 9 wl wl wl wl
OBJ: 1NAT: NCLEX Client Needs Category: Safe, Effective C
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areEnvironment TOP: Nursing Process Step: Assessment
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CON: wl
Patient Education wl
2. Which source contains information specific to nutritional supplements?
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a. USP Dictionary of USAN & International Drug Names
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b. Natural Medicines Comprehensive Database wl wl wl
c. United States Pharmacopoeia/National Formulary (USP NF)
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d. Drug Interaction Facts wl wl
ANS: C wl
United States Pharmacopoeia/National Formulary contains information specific to nutritiona
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lsupplements. USP Dictionary of USAN & International Drug Names is a compilation of d
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rugnames, pronunciation guide, and possible future FDA approved drugs; it does not inclu
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de nutritional supplements. Natural Medicines Comprehensive Database contains
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evidence-
based information on herbal medicines and herbal combination products; it does notinclude i
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nformation specific to nutritional supplements. Drug Interaction Facts contains comprehen
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sive information on drug interaction facts; it does not include nutritional supplements.
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DIF: Cognitive Level: Knowledge REF: p. 4 wl wl w l wl
OBJ: 3NAT: NCLEX Client Needs Category: Physiological Int
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egrity
TOP: Nursing Process Step: Assessment CON: Nutrition | Patient Education
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3. Which drug reference contains drug monographs that describe all drugs in a therapeutic class?
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a. Drug Facts and Comparisons wl wl wl
,Test Bank For Clayton’s Basic Pharmacology for Nurses 19th Editi
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on
b. Drug Interaction Facts wl wl
c. Handbook on Injectable Drugs wl wl wl
d. Martindale—The Complete Drug Reference wl wl wl
ANS: A wl
Drug Facts and Comparisons contains drug monographs that describe all drugs in
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atherapeutic class. Monographs are formatted as tables to allow comparison of simil
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arproducts, brand names, manufacturers, cost indices, and available dosage forms
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Online version is available. wl wl wl
DIF: Cognitive Level: Knowledge REF: p. 4 Table 1.2 wl wl w l wl wl wl
OBJ: 3 wlwlw lNAT: NCLEX Client Needs Category: Physiological Integrity wl wl wl wl wl wl
TOP: Nursing Process Step: Assessment CON: Safety | Patient Education | Clinical Judgment
w l wl wl wl w l wl wl wl wl wl wl
4. Which drug reference contains monographs about virtually every single-
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entity drug availablein the United States and describes therapeutic uses of drugs, includin
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g approved and unapproved uses?
wl wl wl wl
a. Martindale: The Complete Drug Reference wl wl wl wl
b. AHFS Drug Information wl wl
c. Drug Reference wl
d. Drug Facts and Comparisons wl wl wl
ANS: B wl
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 andunapproved uses. wl lw wl
DIF: Cognitive Level: Knowledge REF: p. 4 Table 1.2 wl wl w l wl wl wl
OBJ: 3 wlwlw lNAT: NCLEX Client Needs Category: Physiological Integrity wl wl wl wl wl wl
TOP: Nursing Process Step: Planning
w l CON: Safety | Patient Education | Clinical Judgment
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5. Which online drug reference makes available to healthcare providers and the public a s
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tandard, comprehensive, up-to-date look up and downloadable resource about medicines?
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a. American Drug Index wl wl
b. American Hospital Formulary wl wl
c. DailyMed
d. Drug Reference wl
ANS: C wl
DailyMed makes available to healthcare providers and the public a standard, comprehensiv
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e,up-to-
lw
date look up and downloadable resource about medicines. The American Drug Index isnot
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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 wl wl w l wl wl wl wl
OBJ: 3NAT: 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) wl wl wl wl wl wl
b. Durham Humphrey Amendment (1952) wl wl wl
, Test Bank For Clayton’s Basic Pharmacology for Nurses 19th Editi
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on
c. Controlled Substances Act (1970) wl wl wl
d. Kefauver Harris Drug Amendment (1962) wl wl wl wl
ANS: A wl
The Federal Food, Drug, and Cosmetic Act of 1938 authorized the FDA to determine the s
wl wl wl wl wl wl wl wl wl wl wl wl wl wl wl
afety of all drugs before marketing. Later amendments and acts helped tighten FDA contro
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l and ensure drug safety. The Durham Humphrey Amendment defines the kinds of drugs t
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hat cannot be used safely without medical supervision and restricts their sale to prescriptio
wl wl wl wl wl wl wl wl wl wl wl wl wl
n by a licensed practitioner. The Controlled Substances Act addresses only controlled subst
wl wl wl wl wl wl wl wl wl wl wl wl
ances andtheir categorization. The Kefauver Harris Drug Amendment ensures drug efficacy
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and greaterdrug safety. Drug manufacturers are required to prove to the FDA the effective
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ness of their products before marketing them.
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DIF: Cognitive Level: Knowledge REF: p. 5 Table l.3 wl wl wl wl wl wl
OBJ: 5 w l
NAT: NCLEX Client Needs Category: Physiological Integrit wl wl wl wl wl wl
yTOP: 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 wl
Meperidine (Demerol) is a Schedule II drug; it has a high potential for abuse and may lea
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d tosevere psychological and physical dependence. Schedule I drugs have high potential for
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abuseand no recognized medical use. Schedule III drugs have some potential for abuse. Us
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e may lead to low to moderate physical dependence or high psychological dependence. Sc
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hedule IVdrugs have low potential for abuse. Use may lead to limited physical or psychol
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ogical dependence. wl
DIF: Cognitive Level: Knowledge REF: p. 10 wl wl w l wl
OBJ: 2NAT: NCLEX Client Needs Category: Safe, Effective C
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l wl wl wl wl wl wl wl
are Environment
wl
TOP: Nursing Process Step: Assessment CON: Patient Education | Addiction | Pain
w l wl wl wl w l wl wl wl wl wl
8. Which action would the FDA take to expedite drug development and approval for an outbre
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akof smallpox?
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a. List smallpox as a health orphan disease.
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b. Omit the preclinical research phase. wl wl wl wl
c. Extend the clinical research phase. wl wl wl wl
d. Fast track the investigational drug.
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ANS: D wl
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
wl wl wl wl wl wl wl wl wl wl wl wl wl wl wl wl
manner. Preclinical research is not omitted. Extending any phase of the research would me
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ana longer time to develop a vaccine. The FDA must ensure that all phases of the preclinical
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andclinical research phase have been completed in a safe manner.
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DIF: Cognitive Level: Knowledge wl wl REF: wlwlwl p. 7 wl OBJ: 5 wl
wl wl wl wl wl wl wl wl wl lw
y Michelle J. Willihnganz, Samuel L. Gurevitz, Bruce Clayton Compl
wl wl wl wl wl wl wl wl wl
ete
,Chapter 01: Drug Definitions, Standards, and Information Sources Willihnga
wl wl wl wl wl wl wl wl
nz: Clayton’s Basic Pharmacology for Nurses, 19th Edition
wl wl wl wl wl wl wl
MULTIPLE CHOICE wl
1. Which name identifies a drug listed by the US Food a
wl wl wl wl wl wl wl wl wl wl
ndDrug Administration (FDA)?
lw wl wl
a. Brand
b. Nonproprietary
c. Official
d. Trademark
ANS: C wl
The official name is the name under which a drug is liste
wl wl wl wl w l wl wl wl wl wl wl
d by the FDA. The brand name, or trademark, is the name
wl wl wl wl wl wl wl wl wl wl wl
given to a drug by its manufacturer. The nonproprietary,
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or generic, name is provided by the United States Adopted
wl wl wl wl wl wl wl wl wl
Names Council.
wl wl
DIF: Cognitive Level: Knowledge REF: p. 9 wl wl wl wl
OBJ: 1NAT: NCLEX Client Needs Category: Safe, Effective C
wl wl wl wl wl wl wl wl
areEnvironment TOP: Nursing Process Step: Assessment
w
l wl w l wl wl wl
CON: wl
Patient Education wl
2. Which source contains information specific to nutritional supplements?
wl wl wl wl wl wl wl
a. USP Dictionary of USAN & International Drug Names
wl wl wl wl wl wl wl
b. Natural Medicines Comprehensive Database wl wl wl
c. United States Pharmacopoeia/National Formulary (USP NF)
wl wl wl wl wl
d. Drug Interaction Facts wl wl
ANS: C wl
United States Pharmacopoeia/National Formulary contains information specific to nutritiona
wl wl wl wl wl wl wl wl
lsupplements. USP Dictionary of USAN & International Drug Names is a compilation of d
lw wl wl wl wl wl wl wl wl wl wl wl wl wl
rugnames, pronunciation guide, and possible future FDA approved drugs; it does not inclu
lw wl wl wl wl wl wl wl wl wl wl wl wl
de nutritional supplements. Natural Medicines Comprehensive Database contains
wl wl wl wl wl wl wl
evidence-
based information on herbal medicines and herbal combination products; it does notinclude i
wl wl wl wl wl wl wl wl wl wl wl lw wl
nformation specific to nutritional supplements. Drug Interaction Facts contains comprehen
wl wl wl wl wl wl wl wl wl
sive information on drug interaction facts; it does not include nutritional supplements.
wl wl wl wl wl wl wl wl wl wl wl
DIF: Cognitive Level: Knowledge REF: p. 4 wl wl w l wl
OBJ: 3NAT: NCLEX Client Needs Category: Physiological Int
wl w
l wl wl wl wl wl wl
egrity
TOP: Nursing Process Step: Assessment CON: Nutrition | Patient Education
w l wl wl wl w l wl wl wl
3. Which drug reference contains drug monographs that describe all drugs in a therapeutic class?
wl wl wl wl wl wl wl wl wl wl wl wl wl
a. Drug Facts and Comparisons wl wl wl
,Test Bank For Clayton’s Basic Pharmacology for Nurses 19th Editi
wl wl wl wl wl wl wl wl wl 3
on
b. Drug Interaction Facts wl wl
c. Handbook on Injectable Drugs wl wl wl
d. Martindale—The Complete Drug Reference wl wl wl
ANS: A wl
Drug Facts and Comparisons contains drug monographs that describe all drugs in
wl wl wl wl wl wl wl wl wl wl wl wl
atherapeutic class. Monographs are formatted as tables to allow comparison of simil
lw wl wl wl wl wl wl wl wl wl wl wl
arproducts, brand names, manufacturers, cost indices, and available dosage forms
lw wl wl wl wl wl wl wl wl wl wl
Online version is available. wl wl wl
DIF: Cognitive Level: Knowledge REF: p. 4 Table 1.2 wl wl w l wl wl wl
OBJ: 3 wlwlw lNAT: NCLEX Client Needs Category: Physiological Integrity wl wl wl wl wl wl
TOP: Nursing Process Step: Assessment CON: Safety | Patient Education | Clinical Judgment
w l wl wl wl w l wl wl wl wl wl wl
4. Which drug reference contains monographs about virtually every single-
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entity drug availablein the United States and describes therapeutic uses of drugs, includin
wl wl lw wl wl wl wl wl wl wl wl wl wl
g approved and unapproved uses?
wl wl wl wl
a. Martindale: The Complete Drug Reference wl wl wl wl
b. AHFS Drug Information wl wl
c. Drug Reference wl
d. Drug Facts and Comparisons wl wl wl
ANS: B wl
AHFS Drug Information contains monographs about virtually every single-
wl wl wl wl wl wl wl wl
entity drug available in the United States and describes therapeutic uses of drugs, including
wl wl wl wl wl wl wl wl wl wl wl wl wl wl
approved andunapproved uses. wl lw wl
DIF: Cognitive Level: Knowledge REF: p. 4 Table 1.2 wl wl w l wl wl wl
OBJ: 3 wlwlw lNAT: NCLEX Client Needs Category: Physiological Integrity wl wl wl wl wl wl
TOP: Nursing Process Step: Planning
w l CON: Safety | Patient Education | Clinical Judgment
wl wl wl w l wl wl wl wl wl wl
5. Which online drug reference makes available to healthcare providers and the public a s
wl wl wl wl wl wl wl wl wl wl wl wl wl
tandard, comprehensive, up-to-date look up and downloadable resource about medicines?
wl wl wl wl wl wl wl wl wl
a. American Drug Index wl wl
b. American Hospital Formulary wl wl
c. DailyMed
d. Drug Reference wl
ANS: C wl
DailyMed makes available to healthcare providers and the public a standard, comprehensiv
wl wl wl wl wl wl wl wl wl wl wl
e,up-to-
lw
date look up and downloadable resource about medicines. The American Drug Index isnot
wl wl wl wl wl wl wl wl wl wl wl wl lw wl
appropriate for patient use. The American Hospital Formulary is not appropriate for patie
wl wl wl wl wl wl wl wl wl wl wl wl
nt use. The drug reference is not appropriate for patient use.
wl wl wl wl wl wl wl wl wl wl
DIF: Cognitive Level: Knowledge REF: p. 3 | p. 4 wl wl w l wl wl wl wl
OBJ: 3NAT: NCLEX Client Needs Category: Physiological Int
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l wl wl wl wl wl wl
egrity
TOP: Nursing Process Step: Implementation
wl wl wl wl
CON: Safety | Patient Education | Clinical Judgment
w l wl wl wl wl wl wl
6. Which legislation authorizes the FDA to determine the safety of a drug before its marketing?
wl wl wl wl wl wl wl wl wl wl wl wl wl wl
a. Federal Food, Drug, and Cosmetic Act (1938) wl wl wl wl wl wl
b. Durham Humphrey Amendment (1952) wl wl wl
, Test Bank For Clayton’s Basic Pharmacology for Nurses 19th Editi
wl wl wl wl wl wl wl wl wl 4
on
c. Controlled Substances Act (1970) wl wl wl
d. Kefauver Harris Drug Amendment (1962) wl wl wl wl
ANS: A wl
The Federal Food, Drug, and Cosmetic Act of 1938 authorized the FDA to determine the s
wl wl wl wl wl wl wl wl wl wl wl wl wl wl wl
afety of all drugs before marketing. Later amendments and acts helped tighten FDA contro
wl wl wl wl wl wl wl wl wl wl wl wl wl
l and ensure drug safety. The Durham Humphrey Amendment defines the kinds of drugs t
wl wl wl wl wl wl wl wl wl wl wl wl wl wl
hat cannot be used safely without medical supervision and restricts their sale to prescriptio
wl wl wl wl wl wl wl wl wl wl wl wl wl
n by a licensed practitioner. The Controlled Substances Act addresses only controlled subst
wl wl wl wl wl wl wl wl wl wl wl wl
ances andtheir categorization. The Kefauver Harris Drug Amendment ensures drug efficacy
wl lw wl wl wl wl wl wl wl wl wl
and greaterdrug safety. Drug manufacturers are required to prove to the FDA the effective
wl wl lw wl wl wl wl wl wl wl wl wl wl wl wl
ness of their products before marketing them.
wl wl wl wl wl wl
DIF: Cognitive Level: Knowledge REF: p. 5 Table l.3 wl wl wl wl wl wl
OBJ: 5 w l
NAT: NCLEX Client Needs Category: Physiological Integrit wl wl wl wl wl wl
yTOP: Nursing Process Step: Assessment
w
l wl wl wl wl
CON: Safety | Patient Education | Evidence | Health Care Law
w l wl wl wl wl wl wl wl wl wl
7. Which classification does meperidine (Demerol) fall under?
wl wl wl wl wl wl
a. I
b. II
c. III
d. IV
ANS: B wl
Meperidine (Demerol) is a Schedule II drug; it has a high potential for abuse and may lea
wl wl wl wl wl wl wl wl wl wl wl wl wl wl wl wl
d tosevere psychological and physical dependence. Schedule I drugs have high potential for
wl lw wl wl wl wl wl wl wl wl wl wl wl wl
abuseand no recognized medical use. Schedule III drugs have some potential for abuse. Us
lw wl wl wl wl wl wl wl wl wl wl wl wl wl
e may lead to low to moderate physical dependence or high psychological dependence. Sc
wl wl wl wl wl wl wl wl wl wl wl wl wl
hedule IVdrugs have low potential for abuse. Use may lead to limited physical or psychol
wl lw wl wl wl wl wl wl wl wl wl wl wl wl wl
ogical dependence. wl
DIF: Cognitive Level: Knowledge REF: p. 10 wl wl w l wl
OBJ: 2NAT: NCLEX Client Needs Category: Safe, Effective C
wl w
l wl wl wl wl wl wl wl
are Environment
wl
TOP: Nursing Process Step: Assessment CON: Patient Education | Addiction | Pain
w l wl wl wl w l wl wl wl wl wl
8. Which action would the FDA take to expedite drug development and approval for an outbre
wl wl wl wl wl wl wl wl wl wl wl wl wl wl
akof smallpox?
lw wl
a. List smallpox as a health orphan disease.
wl wl wl wl wl wl
b. Omit the preclinical research phase. wl wl wl wl
c. Extend the clinical research phase. wl wl wl wl
d. Fast track the investigational drug.
wl wl wl wl
ANS: D wl
Once the Investigational New Drug Application has been approved, the drug can receive h
wl wl wl wl wl wl wl wl wl wl wl wl wl
ighest priority within the agency, which is called fast tracking. A smallpox outbreak would
wl wl wl wl wl wl wl wl wl wl wl wl wl
become a priority concern in the world. Orphan diseases are not researched in a priority
wl wl wl wl wl wl wl wl wl wl wl wl wl wl wl wl
manner. Preclinical research is not omitted. Extending any phase of the research would me
wl wl wl wl wl wl wl wl wl wl wl wl wl
ana longer time to develop a vaccine. The FDA must ensure that all phases of the preclinical
lw wl wl wl wl wl wl wl wl wl wl wl wl wl wl wl wl
andclinical research phase have been completed in a safe manner.
wl lw wl wl wl wl wl wl wl wl wl
DIF: Cognitive Level: Knowledge wl wl REF: wlwlwl p. 7 wl OBJ: 5 wl