TEST BANK PHARMACOLOGY FOR NURSES A PATHOPHYSIOLOGY APPROACH BY MICHAEL ADAMS LATEST UPDATED 2024 QUESTIONS WITH DETAILED ANSWERS ALL CHAPTERS INCLUDED WITH COMPLETE SOLUTIONS

TEST BANK PHARMACOLOGY FOR NURSES A PATHOPHYSIOLOGY APPROACH BY MICHAEL ADAMS LATEST
UPDATED 2024 QUESTIONS WITH DETAILED ANSWERS ALL CHAPTERS INCLUDED WITH
COMPLETE SOLUTIONS

, Chapter

1. The pharmaceutical representative comes to the physician's office and says his company's
pharmaceutical laboratory is marketing a drug that does not need approval by the Food and
Drug Administration (FDA). What is the best response by the nurse?

2. "Any pharmaceutical laboratory in America must have approval from the Food and Drug
Administration (FDA) before marketing a drug."

3. "Is this an over-the-counter (OTC) drug? They do not need approval by the Food and
Drug Administration (FDA)."

4. "Is your pharmaceutical laboratory private? Only public pharmaceutical laboratories
need approval from the Food and Drug Administration (FDA)."

5. "Your pharmaceutical laboratory must be involved in academic research because they
are exempt from approval by the Food and Drug Administration (FDA)."

Correct Answer: 1

,Rationale 1: Any pharmaceutical laboratory must obtain approval from the Food and Drug
Administration (FDA) before marketing a drug.

Rationale 2: Pharmaceutical laboratories that manufacture over-the-counter (OTC) drugs must
obtain approval from the Food and Drug Administration (FDA) before marketing these drugs.

Rationale 3: Private pharmaceutical laboratories must obtain approval from the Food and Drug
Administration (FDA) before marketing a drug.

Rationale 4: Pharmaceutical laboratories involved in academic research must obtain approval
from the Food and Drug Administration (FDA) before marketing a drug.

Global Rationale: Any pharmaceutical laboratory, whether private, public, or academic, must
obtain approval from the Food and Drug Administration (FDA) before marketing a drug. Private
pharmaceutical laboratories must obtain approval from the Food and Drug Administration
(FDA) before marketing a drug. Pharmaceutical laboratories involved in academic research
must obtain approval from the Food and Drug Administration (FDA) before marketing a drug.
Pharmaceutical laboratories that manufacture over-the-counter (OTC) drugs must obtain
approval from the Food and Drug Administration (FDA) before marketing these drugs.

Cognitive Level: Applying
Client Need: Physiological Integrity
Client Need Sub: Pharmacological and Parenteral Therapies
QSEN Competencies: V.B.1 Demonstrate effective use of technology and standardized
practices that support safety and quality.
AACN Essential Competencies: V.4 Examine legislative and regulatory processes relevant to
the provision of health care.
NLN Competencies: Quality and Safety: Policies and procedures.
Nursing/Integrated Concepts: Nursing Process: Implementation
Learning Outcome: 2-2 Discuss the role of the U.S. Food and Drug Administration (FDA) in
the drug approval process.
MNL Learning Outcome: 1.1.1 Apply basic concepts related to pharmacology.
Page Number: 13


Type:
MCSA

2. The nurse is employed by the Food and Drug Administration (FDA) and is involved in
clinical investigation. What is the primary role of the nurse in this phase of the review and
approval process by the FDA?

1. To perform tests on the population-at-large

, 2. To perform tests on various species of animals

3. To perform tests on human cells cultured in the laboratory

4. To perform tests on human clients

Correct Answer: 4

Rationale 1: Performing tests on the population-at-large is the stage of post-marketing
surveillance.

Rationale 2: Performing tests on various species of animals is the preclinical investigation stage.

Rationale 3: Performing tests on human cells cultured in the laboratory is the preclinical
investigation stage.

Rationale 4: Clinical investigation includes performing tests on healthy volunteers, and later, on
selected clients with a particular disease.

Global Rationale: Clinical investigation includes performing tests on healthy volunteers, and
later, on selected clients with a particular disease. Performing tests on human cells cultured in the
laboratory is the preclinical investigation stage. Performing tests on the population-at-large is the
stage of post-marketing surveillance. Performing tests on various species of animals is the
preclinical investigation stage.

Cognitive Level: Applying
Client Need: Physiological Integrity
Client Need Sub: Pharmacological and Parenteral Therapies
QSEN Competencies: V.B.1 Demonstrate effective use of technology and standardized
practices that support safety and quality.
AACN Essential Competencies: V.4 Examine legislative and regulatory processes relevant to
the provision of health care.
NLN Competencies: Quality and Safety: Policies and procedures.
Nursing/Integrated Concepts: Nursing Process: Implementation
Learning Outcome: 2-5 Identify the nurse’s role in the drug approval process and in maintaining
safety practices.
MNL Learning Outcome: 1.1.1 Apply basic concepts related to pharmacology.
Page Number: 13

Type:
MCSA