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NURS 306: MODULE 1 EXAM QUESTIONS AND ANSWERS WITH COMPLETE SOLUTIONS VERIFIED LATEST UPDATE GRADED A 2025/2026 VERSION | ASSURED SUCCESS

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NURS 306: MODULE 1 EXAM QUESTIONS AND ANSWERS WITH COMPLETE SOLUTIONS VERIFIED LATEST UPDATE GRADED A 2025/2026 VERSION | ASSURED SUCCESS

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8/17/25, 10:22
AM

NURS 306: MODULE 1 EXAM QUESTIONS AND
ANSWERS WITH COMPLETE SOLUTIONS
VERIFIED LATEST UPDATE GRADED A
2025/2026 VERSION | ASSURED SUCCESS

Terms in this set (52)



Pharmacology is best the study of the biological effects of chemicals
defined as _____________
A drug is assigned a C-II 3. Food and Drug Administration (FDA)
abuse potential during
the third phase of
testing, which
organization is most likely
to be involved during
this process?


1. Froggies and
Dinosaur's Associates
(FDA)
2. Drug Enforcement
Agency (DEA)
3. Food and Drug
Administration (FDA)
Your attending We can't be in the first phase of testing
physician says that the because during the first phase of testing we
first phase of clinical use human volunteers (that are fully informed
1/
22

,8/17/25, 10:22
AM
trials is going well of the potential effects and are often
because none of the compensated) to test the drugs. You must be
monkeys reacted talking about the pre-clinical trials.
adversely to the drugs,
as the nurse, what
should you politely
tell them?
Your attending If the drug you're testing has teratogenic
physician brings in a effects, you may permanently destroy the
group of 8 women and reproductive system of the 8 females
4 men for the first involved. Clinical trials should typically
phase of testing, what incorporate a majority male test group.
is your biggest concern
as a nurse?
You are assigned to a Phase II
study where clinical
investigators selectively
test a new drug on
patients who have the
disease the drug is
designed to treat, what
phase is your study in?




2/
22

, 8/17/25, 10:22
AM



The case you've been Phase III
assigned to
distributes a new drug
widely across the
clinical space - you are
charged to observe the
patient's reactions
carefully, report any
adverse reactions to
the FDA, and ask
patients to keep a
journal, which phase is
your study in?
Before submitting 1. Generic name (Ibuprofen)
your drug into the 2. Brand name (Advil)
FDA for approval you
had given it a name.
After being approved
you've been allowed
to name the drug
again and have given
the rights to a patent
on the drug. What are
these two names
formally referred to
as?
Which phase is a drug in Phase IV
if it is described to be

3/
22

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