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