TEST BANK FOR RAUS
RESPIRATORY CARE
PHARMACOLOGY
10TH EDITION BY
GARDENHIRE
,Chapter 01: Introduction to Respiratory Care
Pharmacology Gardenhire: Rau’s Respiratory Care
Pharmacology, 10th Edition
MULTIPLE CHOICE
1. The listing of a drug and the amount of drug are found in which part of a prescription?
a. Superscription
b. Inscription
c. Subscription
d. Transcription (signature)
ANS: B
The superscription directs the pharmacist to take the drug listed and prepare the
medication; the inscription lists the name and quantity of the drug being prescribed; the
subscription provides directions to the pharmacist for preparing the medication; and the
transcription, or signature, is the information the pharmacist writes on the label as
instructions to the patient.
REF: p. 7
2. If generic substitution is permitted on a prescription:
a. drug from only one manufacturer must be given.
b. drug formulation may be changed by the pharmacist.
c. any manufactured brand of the drug listed may be given.
d. drug strength may be changed by the pharmacist.
ANS: C
A generic substitution allows any brand of a drug to be given, but the pharmacist may
not change a drug formulation without specific permission from the prescribing
physician. A physician can indicate to the pharmacist that generic substitution is
permitted in the filling of the prescription. In such a case, the pharmacist may provide
any manufacturer’s version of the prescribed drug, rather than a specific brand.
However, the pharmacist may not change the strength of a drug without specific
permission from the prescribing physician.
REF: p. 8
,3. The study of drugs, including their origin, properties, and interactions with living
organisms, is known as
a. pharmacogenetics.
b. pharmacology.
c. therapeutics.
d. toxicology.
ANS: B
Pharmacogenetics is the study of the interrelationship of genetic differences and drug
effects. Pharmacology is the study of drugs (chemicals), including their origin,
properties, and interactions with living organisms.
Therapeutics is the art of treating disease with drugs. Toxicology is the study of toxic
substances and their pharmacologic actions, including antidotes and poison control.
REF: p. 3
4. The brand name given to a drug by a particular manufacturer is known as the drug’s
a. chemical name.
b. generic name. c. official name. d. trade name.
ANS: D
The chemical name indicates the drug’s chemical structure. The generic name is assigned
by the United States Adopted Name Council and is usually based loosely on the drug’s
chemical structure. The official name is the
, name given to the generic name once a drug becomes fully approved for general use
and is admitted to the United States Pharmacopeia–National Formulary. The trade name
is the brand, or proprietary, name given by a particular manufacturer. For example, the
generic drug albuterol is currently marketed by Schering-Plough as Proventil® and by
GlaxoSmithKline as Ventolin®.
REF: p. 5
5. To find official information about drugs (according to the FDA), you need to go to the
a. Physician’s Desk Reference (PDR).
b. Basic & Clinical Pharmacology.
c. United States Pharmacopeia–National Formulary (USP-NF).
d. Goodman & Gilman’s The Pharmacological Basis of Therapeutics.
ANS: C
Because the PDR is prepared by drug manufacturers themselves, it may be lacking in
objectivity. Basic & Clinical Pharmacology covers only general pharmacologic principles
and drug classes. Goodman & Gilman’s The Pharmacological Basis of Therapeutics
covers only general pharmacologic principles and drug classes. The USP-NF is a book of
standards containing information about medications, dietary supplements, and medical
devices. The U.S. Food and Drug Administration (FDA) considers this book the official
standard for drugs marketed in the United States.
REF: p. 5
. 1
RESPIRATORY CARE
PHARMACOLOGY
10TH EDITION BY
GARDENHIRE
,Chapter 01: Introduction to Respiratory Care
Pharmacology Gardenhire: Rau’s Respiratory Care
Pharmacology, 10th Edition
MULTIPLE CHOICE
1. The listing of a drug and the amount of drug are found in which part of a prescription?
a. Superscription
b. Inscription
c. Subscription
d. Transcription (signature)
ANS: B
The superscription directs the pharmacist to take the drug listed and prepare the
medication; the inscription lists the name and quantity of the drug being prescribed; the
subscription provides directions to the pharmacist for preparing the medication; and the
transcription, or signature, is the information the pharmacist writes on the label as
instructions to the patient.
REF: p. 7
2. If generic substitution is permitted on a prescription:
a. drug from only one manufacturer must be given.
b. drug formulation may be changed by the pharmacist.
c. any manufactured brand of the drug listed may be given.
d. drug strength may be changed by the pharmacist.
ANS: C
A generic substitution allows any brand of a drug to be given, but the pharmacist may
not change a drug formulation without specific permission from the prescribing
physician. A physician can indicate to the pharmacist that generic substitution is
permitted in the filling of the prescription. In such a case, the pharmacist may provide
any manufacturer’s version of the prescribed drug, rather than a specific brand.
However, the pharmacist may not change the strength of a drug without specific
permission from the prescribing physician.
REF: p. 8
,3. The study of drugs, including their origin, properties, and interactions with living
organisms, is known as
a. pharmacogenetics.
b. pharmacology.
c. therapeutics.
d. toxicology.
ANS: B
Pharmacogenetics is the study of the interrelationship of genetic differences and drug
effects. Pharmacology is the study of drugs (chemicals), including their origin,
properties, and interactions with living organisms.
Therapeutics is the art of treating disease with drugs. Toxicology is the study of toxic
substances and their pharmacologic actions, including antidotes and poison control.
REF: p. 3
4. The brand name given to a drug by a particular manufacturer is known as the drug’s
a. chemical name.
b. generic name. c. official name. d. trade name.
ANS: D
The chemical name indicates the drug’s chemical structure. The generic name is assigned
by the United States Adopted Name Council and is usually based loosely on the drug’s
chemical structure. The official name is the
, name given to the generic name once a drug becomes fully approved for general use
and is admitted to the United States Pharmacopeia–National Formulary. The trade name
is the brand, or proprietary, name given by a particular manufacturer. For example, the
generic drug albuterol is currently marketed by Schering-Plough as Proventil® and by
GlaxoSmithKline as Ventolin®.
REF: p. 5
5. To find official information about drugs (according to the FDA), you need to go to the
a. Physician’s Desk Reference (PDR).
b. Basic & Clinical Pharmacology.
c. United States Pharmacopeia–National Formulary (USP-NF).
d. Goodman & Gilman’s The Pharmacological Basis of Therapeutics.
ANS: C
Because the PDR is prepared by drug manufacturers themselves, it may be lacking in
objectivity. Basic & Clinical Pharmacology covers only general pharmacologic principles
and drug classes. Goodman & Gilman’s The Pharmacological Basis of Therapeutics
covers only general pharmacologic principles and drug classes. The USP-NF is a book of
standards containing information about medications, dietary supplements, and medical
devices. The U.S. Food and Drug Administration (FDA) considers this book the official
standard for drugs marketed in the United States.
REF: p. 5
. 1
