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MN 553/ MN553 Advanced Pharmacology Unit 8 Exam (Latest 2026/2027 Update) | Complete Exam Questions with Verified Answers and Detailed Rationales | Cholinergic Agents | A+ Graded | Purdue University Global

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INSTANT PDF DOWNLOAD - This is the comprehensive Unit 8 Exam study guide for MN 553 Advanced Pharmacology at Purdue University Global (Latest 2026/2027 Update), featuring 100% verified exam questions with correct answers and detailed rationales covering cholinergic and adrenergic pharmacology, CNS/PNS agents, and key prescribing principles . This resource covers cholinergic agents including direct-acting (Bethanechol, Pilocarpine) and indirect-acting (cholinesterase inhibitors like Neostigmine) ; cholinergic/adrenergic effects (bronchoconstriction vs bronchodilation, pupil changes) ; clinical uses of alpha blockers (prazosin, tamsulosin for HTN and BPH) and beta blockers (angina, HTN, heart failure, migraine prophylaxis) ; autonomic nervous system pharmacology; CNS agents including anticonvulsants (phenytoin, lamotrigine), antidepressants (SSRIs, SNRIs, TCAs), antipsychotics (typical and atypical), anxiolytics (benzodiazepines, buspirone), and stimulants (methylphenidate, amphetamines for ADHD). Aligned with Purdue Global MN 553 curriculum and NP certification standards. MN 553 Unit 8 Exam Purdue MN553 Advanced Pharmacology Unit 8 Cholinergic agents parasympathomimetics muscarinic agonists Bethanechol Urecholine increases bladder tone detrusor muscle Pilocarpine glaucoma treatment Cholinesterase inhibitors neostigmine pyridostigmine Main uses cholinergic drugs glaucoma GI atony urinary retention myasthenia gravis Cholinergic effects constricted pupils increased saliva bronchoconstriction increased GI mucus Adrenergic effects dry mouth dilated pupils increased HR bronchodilation Alpha blocker medications prazosin tamsulosin doxazosin Clinical uses alpha blockers hypertension benign prostatic hyperplasia BPH Beta blocker clinical uses angina HTN heart failure tachycardia post MI migraine prophylaxis Autonomic nervous system pharmacology Anticonvulsants hydantoins phenytoin lamotrigine Antidepressant classes SSRIs SNRIs TCAs MAOIs Fluoxetine Prozac first line pediatric depression SSRI adverse effects CNS GI sexual dysfunction serotonin syndrome SNRI clinical uses major depressive disorder GAD neuropathy fibromyalgia Antipsychotic categories typical atypical First generation antipsychotics chlorpromazine haloperidol Atypical antipsychotics clozapine risperidone olanzapine quetiapine Second generation antipsychotics EPS risk lower weight gain higher Anxiolytics benzodiazepines buspirone Buspirone onset 2 weeks maximum effect 6 weeks cannot treat panic attacks Benzodiazepine uses anxiety insomnia ADHD pharmacotherapy stimulants methylphenidate amphetamines Methylphenidate Ritalin side effects insomnia appetite suppression Nonstimulant ADHD atomoxetine Strattera Migraine treatment triptans sumatriptan contraindicated CAD uncontrolled HTN pregnancy Migraine preventive medication goal reduce occurrence 50 percent Gabapentin adverse effects depression strange thoughts assess suicidal ideation Ergotamine suppository migraine acute treatment Purdue University Global MN553 A+ Grade Pharmacology Study Guide

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Purdue University Global




8 TINU • 355NM
★ ★




P School of Nursing · MN553 Advanced Pharmacology
M A K I N G T H E D I F F E R E N C E · C A R E E R- O R I E N T E D H I G H E R E D U C AT I O N
EST. 1998




MN553 — Unit 8 Examination
A D VA N C E D P H A R M A CO LO G Y: A N S , C N S & PA I N M A N A G E M E N T

INSTITUTION Purdue University Global COURSE CODE MN553
PROGRAM Master of Science in Nursing (MSN-FNP) ACADEMIC YEAR
EXAM TITLE Unit 8 — Comprehensive Pharmacology TOTAL QUESTIONS 25 Questions
COURSE TITLE Advanced Pharmacology for Advanced FORMAT Multiple Choice — Select the Single Best
Practice Nursing Answer


UNIT 8 EXAMINATION INSTRUCTIONS
▸ Select the single best answer for each question.
▸ Content covers cholinergic/adrenergic agents, antidepressants, antipsychotics, anxiolytics, ADHD medications, migraine
therapy, and pain management.
▸ Correct answers and clinical rationales appear below each question for board review and clinical application.
▸ Pay careful attention to drug interactions, contraindications, monitoring parameters, and special population considerations.


SECTION I — AUTONOMIC, CNS PHARMACOLOGY & PAIN Questions 1 –
THERAPEUTICS 25

1. A patient taking a cholinergic agonist reports constricted pupils, increased salivation, and bronchoconstriction.
These effects are classified as:
A. Adrenergic effects — sympathetic nervous system activation
B. Cholinergic effects — parasympathetic nervous system activation
C. Anticholinergic effects — blocking parasympathetic activity
D. Dopaminergic effects — central dopamine pathway activation
CORRECT ANSWER B — Cholinergic effects — parasympathetic nervous system activation

RATIONALE Cholinergic effects result from parasympathetic nervous system activation and include: constricted pupils
(miosis), increased saliva, bronchoconstriction, increased GI mucus, and bladder fundus contraction.
Adrenergic effects (sympathetic) produce the opposite: dry mouth, dilated pupils, increased heart
rate/contractility, bronchodilation, and bladder fundus relaxation. This fundamental ANS distinction is critical
for understanding drug actions and predicting adverse effects.

, 2. Prazosin (Minipress) and Tamsulosin (Flomax) are alpha blocker medications. What are their primary clinical uses?
A. Angina and migraine prophylaxis
B. Heart failure and post-MI antidysrhythmias
C. Hypertension (HTN) and benign prostatic hyperplasia (BPH)
D. Asthma and COPD
CORRECT ANSWER C — Hypertension (HTN) and benign prostatic hyperplasia (BPH)

RATIONALE Alpha blockers like Prazosin and Tamsulosin are primarily used for hypertension (by reducing peripheral
vascular resistance) and BPH (by relaxing smooth muscle in the bladder neck and prostate, improving urine
flow). Beta blockers are used for angina, HTN, heart failure, tachycardia, post-MI antidysrhythmias, and
migraine prophylaxis. Asthma/COPD are not treated with alpha blockers. This distinction between alpha and
beta blocker indications is essential for safe prescribing.


3. Bethanechol (Urecholine) increases detrusor muscle tone and causes bladder contractions. What is its primary
clinical use?
A. Treatment of overactive bladder
B. Neurogenic bladder atony
C. Gastroesophageal reflux disease (GERD)
D. Urinary incontinence
CORRECT ANSWER B — Neurogenic bladder atony

RATIONALE Bethanechol is a direct-acting cholinergic drug that increases detrusor muscle tone and stimulates bladder
contractions. It is used specifically for neurogenic bladder atony — a condition where the bladder lacks
muscle tone. It is NOT used for GERD/reflux — the statement "Bethanechol can be used for reflux" is FALSE.
Overactive bladder and urinary incontinence are treated with anticholinergics (e.g., oxybutynin), not
cholinergics. Understanding the clinical applications of cholinergic vs. anticholinergic drugs is essential.


4. Which of the following is a direct-acting cholinergic drug used to decrease intraocular pressure in glaucoma?
A. Neostigmine bromide (Prostigmin) — indirect-acting cholinesterase inhibitor
B. Pilocarpine (Pilocar) — direct-acting muscarinic agonist
C. Scopolamine — anticholinergic blocker
D. Benztropine — anticholinergic for Parkinsonism
CORRECT ANSWER B — Pilocarpine (Pilocar) — direct-acting muscarinic agonist

RATIONALE Pilocarpine is a direct-acting cholinergic drug (muscarinic agonist) used to decrease intraocular pressure in
glaucoma. Direct-acting cholinergic drugs also include Bethanechol. Indirect-acting cholinergic drugs
(cholinesterase inhibitors) include Neostigmine. The main uses of cholinergic drugs are: decrease IOP in
glaucoma, treat atony of GI tract and urinary bladder, and diagnose/treat myasthenia gravis. Scopolamine
and Benztropine are anticholinergic blockers, not cholinergic agents.

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