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Test Bank - Rau's Respiratory Care Pharmacology 11th Edition by (Douglas S. Gardenhire, 2023) All Chapters 1-23

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Complete Test Bank Rau's Respiratory Care Pharmacology 11th Edition by Douglas S. Gardenhire All Chapters 1 -23| Latest| A+ PASS Table of Contents Unit I: Basic Concepts and Principles in Pharmacology 1. Introduction to Respiratory Care Pharmacology 2. Principles of Drug Action 3. Administration of Aerosolized Agents 4. Calculating Drug Doses 5. The Central and Peripheral Nervous Systems Unit II: Drugs Used to Treat the Respiratory System 6. Adrenergic (Sympathomimetic) Bronchodilators 7. Anticholinergic (Parasympatholytic) Bronchodilators 8. Xanthines 9. Mucus-Controlling Drug Therapy 10. Surfactant Agents 11. Corticosteriods in Respiratory Care 12. Nonsteroidal Antiasthma Agents 13. Aerosolized Antiinfective Agents 14. Antimicrobial Agents 15. Cold and Cough Agents 16. Selected Agents of Pulmonary Value 17. Neonatal and Pediatric Aerosolized Drug Therapy Unit III: Critical Care, Cardiovascular, and Polysomnography Agents 18. Skeletal Muscle Relaxants (Neuromuscular Blocking Agents) 19. Diuretic Agents 20. Drugs Affecting the Central Nervous System 21. Vasopressors, Inotropes, and Antiarrythmic Agents 22. Drugs Affecting Circulation: Antihypertensives, Antianginals, Antithrombotics 23. Sleep and Sleep Pharmacology

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Complete Test Bank
Rau's Respiratory Care Pharmacology
11th Edition
by Douglas S. Gardenhire
All Chapters 1-23| Latest| A+ PASS
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Table of Contents
Unit I: Basic Concepts and Principles in Pharmacology

1. Introduction to Respiratory Care Pharmacology

2. Principles of Drug Action

3. Administration of Aerosolized Agents

4. Calculating Drug Doses

5. The Central and Peripheral Nervous Systems

Unit II: Drugs Used to Treat the Respiratory System

6. Adrenergic (Sympathomimetic) Bronchodilators

7. Anticholinergic (Parasympatholytic) Bronchodilators

8. Xanthines

9. Mucus-Controlling Drug Therapy

10. Surfactant Agents

11. Corticosteriods in Respiratory Care

12. Nonsteroidal Antiasthma Agents

13. Aerosolized Antiinfective Agents

14. Antimicrobial Agents

15. Cold and Cough Agents
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16. Selected Agents of Pulmonary Value
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17. Neonatal and Pediatric Aerosolized Drug Therapy

Unit III: Critical Care, Cardiovascular, and Polysomnography Agents
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18. Skeletal Muscle Relaxants (Neuromuscular Blocking Agents)
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19. Diuretic Agents
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20. Drugs Affecting the Central Nervous System
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21. Vasopressors, Inotropes, and Antiarrythmic Agents

22. Drugs Affecting Circulation: Antihypertensives, Antianginals, Antithrombotics
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23. Sleep and Sleep Pharmacology
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Chapter 01: Introduction to Respiratory Care Pharmacology
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.
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ANS: C
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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
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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
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prescribing physician.

REF: p. 8
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3. The study of drugs, including their origin, properties, and interactions with living organisms, is known
as
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a. pharmacogenetics.
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b. pharmacology.
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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
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5. To find official information about drugs (according to the FDA), you need to go to the

a. Physician’s Desk Reference (PDR).
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b. Basic & Clinical Pharmacology.
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c. United States Pharmacopeia–National Formulary (USP-NF).

d. Goodman & Gilman’s The Pharmacological Basis of Therapeutics.
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ANS: C
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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 &
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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
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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.
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REF: p. 5
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