Test Bank For Abrams’ Clinical Drug Therapy Rationales for Nursing Practice 12th Edition Geralyn Frandsen

TEST BANK
ABRAMS’ CLINICAL DRUG THERAPY RATIONALES FOR NURSING
PRACTICE 12TH EDITION
GERALYN FRANDSEN

Chapter 1, The Foundation of Pharmacology: Quality and Safety

  1. A woman diagnosed with obsessive–compulsive disorder has been prescribed oral
    paroxetine hydrochloride. What is the expected effect for this prescription?
    A. Curative effect on symptoms
    B. Systemic effect on symptoms
    C. Local effect on symptoms
    D. Parenteral effect on symptoms
    ANS: B
    Rationale: Drugs that produce systemic effects are taken into the body, circulated through
    the bloodstream to their sites of action in various body tissues, and eventually eliminated
    from the body. Curative agents are given to cure a disease process. In this case, paroxetine
    hydrochloride will control the symptoms but not cure the disorder. Drugs with local effects,
    such as sunscreen and local anesthetics, act mainly at the site of application. Paroxetine
    hydrochloride is not administered parenterally. Parenteral agents are administered
    subcutaneously, intramuscularly, or intravenously.
    PTS: 1 REF: p. 3, Introduction OBJ: 1
    NAT: Client Needs: Physiological Integrity: Pharmacological and Parenteral Therapies
    TOP: Chapter: 1: The Foundation of Pharmacology: Quality and Safety
    KEY: Integrated Process: Nursing Process
    BLM: Cognitive Level: Understand NOT: Multiple Choice
  2. A client has been prescribed an antibiotic. This medication is a naturally occurring
    substance that has been chemically modified. What is another name for this type of
    medication?
    A. Synthetic drug
    B. Semisynthetic drug
    C. Biotechnology drug
    D. Prototype drug
    ANS: B
    Rationale: Semisynthetic drugs (e.g., many antibiotics) are naturally occurring substances
    that have been chemically modified. Synthetic drugs are more standardized in their chemical
    characteristics, more consistent in their effects, and less likely to produce allergic reactions.
    Biotechnology drugs involve manipulating DNA and RNA and recombining genes into
    hybrid molecules that can be inserted into living organisms. Prototype drugs are the first
    drug of a particular group to be developed.
    PTS: 1 REF: p. 3, Drug Sources OBJ: 1
    NAT: Client Needs: Physiological Integrity: Pharmacological and Parenteral Therapies
    TOP: Chapter: 1: The Foundation of Pharmacology: Quality and Safety
    KEY: Integrated Process: Nursing Process
    BLM: Cognitive Level: Understand NOT: Multiple Choice
  3. Which classification applies to morphine?
    A. Central nervous system depressant
    B. Central nervous system stimulant

C. Anti-inflammatory
D. Antihypertensive
ANS: A
Rationale: Drugs are classified according to their effects on particular body systems, their
therapeutic uses, and their chemical characteristics. Morphine is classified as a central
nervous system depressant and will produce this effect in the client. A central nervous
system stimulant increases attention and raises mood. An anti-inflammatory agent decreases
inflammation at the site of tissue or joint inflammation. An antihypertensive agent reduces
blood pressure.
PTS: 1 REF: p. 3, Drug Classifications and Prototypes
OBJ: 1
NAT: Client Needs: Physiological Integrity: Pharmacological and Parenteral Therapies
TOP: Chapter: 1: The Foundation of Pharmacology: Quality and Safety
KEY: Integrated Process: Nursing Process
BLM: Cognitive Level: Remember NOT: Multiple Choice

  1. A client is administered amoxicillin. The generic name of this medication belongs to which
    drug group?
    A. Selective serotonin reuptake inhibitors
    B. Diuretics
    C. Penicillins
    D. ACE inhibitors
    ANS: C
    Rationale: The generic name often indicates the drug group (e.g., drugs with generic names
    ending in “cillin” are penicillins). Selective serotonin reuptake inhibitors are medications
    that have antidepressant effects; SSRI is a broad classification, not a generic name. Diuretics
    are medications that increase urine output; diuretic is a broad classification, not a generic
    name. ACE inhibitor is the broad classification for the angiotensin receptor blockers, not the
    generic name.
    PTS: 1 REF: p. 3, Drug Names OBJ: 2
    NAT: Client Needs: Physiological Integrity: Pharmacological and Parenteral Therapies
    TOP: Chapter: 1: The Foundation of Pharmacology: Quality and Safety
    KEY: Integrated Process: Nursing Process
    BLM: Cognitive Level: Understand NOT: Multiple Choice
  2. The administration of diphenhydramine is regulated by which U.S. government agency?
    A. Public Health Service
    B. Federal Trade Commission
    C. Occupational Safety and Health Administration
    D. Food and Drug Administration
    ANS: D

Rationale: The Food and Drug Administration approves drugs for over-the-counter
availability, including the transfer of drugs from prescription to OTC status, and may
require clinical trials to determine the safety and effectiveness of OTC use. The Public
Health Service is regulated by the state to maintain the health of individual citizens of the
state. The Federal Trade Commission regulates imports and exports throughout the nation.
The Occupational Safety and Health Administration regulates safety within the workplace.
PTS: 1 REF: p. 4, Prescription and Nonprescription Drugs
OBJ: 4
NAT: Client Needs: Physiological Integrity: Pharmacological and Parenteral Therapies
TOP: Chapter: 1: The Foundation of Pharmacology: Quality and Safety
KEY: Integrated Process: Nursing Process
BLM: Cognitive Level: Understand NOT: Multiple Choice

  1. In the U.S., the administration of anabolic steroids is regulated by which law?
    A. The Food, Drug, and Cosmetic Act of 1938
    B. The Comprehensive Drug Abuse Prevention and Control Act
    C. The Harrison Narcotic Act
    D. The Sherley Amendment
    ANS: B
    Rationale: The Comprehensive Drug Abuse Prevention and Control Act regulates the
    manufacture and distribution of narcotics, stimulants, depressants, hallucinogens, and
    anabolic steroids. The Food, Drug, and Cosmetic Act of 1938 revised and broadened FDA
    powers and responsibilities, giving the FDA control over drug safety. The Harrison Narcotic
    Act restricted the importation, manufacture, sale, and use of opium, cocaine, marijuana, and
    other drugs that the act defined as narcotics. The Sherley Amendment of 1912 prohibited
    fraudulent claims of drug effectiveness.
    PTS: 1 REF: p. 4, Prescription and Nonprescription Drugs
    OBJ: 3
    NAT: Client Needs: Physiological Integrity: Pharmacological and Parenteral Therapies
    TOP: Chapter: 1: The Foundation of Pharmacology: Quality and Safety
    KEY: Integrated Process: Nursing Process
    BLM: Cognitive Level: Remember NOT: Multiple Choice
  2. A nurse is responsible for maintaining an accurate count and record of the controlled
    substances on the nursing division. This nursing action is regulated by which U.S. law or
    agency?
    A. The Food, Drug, and Cosmetic Act of 1938
    B. The Public Health Service
    C. The Drug Enforcement Administration
    D. The Sherley Amendment
    ANS: C

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