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NR 546 Week 10 Exam V1 | NR 546 Advanced Pharmacology Psychopharmacology for the PMHNP | Actual Q&A with Rationale (NR546 Week 10 Exam) | Chamberlain University

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NR 546 Week 10 Exam V1 | NR 546 Advanced Pharmacology Psychopharmacology for the PMHNP | Actual Q&A with Rationale (NR546 Week 10 Exam) | Chamberlain University

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NR 546 Week 10 Exam V1 | NR 546 Advanced
Pharmacology Psychopharmacology for the
PMHNP | Actual Q&A with Rationale (NR546 Week
10 Exam) | Chamberlain University
1. Which of the following is the primary mechanism of action for methylphenidate in the

treatment of ADHD?

A. Selective inhibition of the norepinephrine transporter (NET) only.


B. Promotion of dopamine release from presynaptic storage vesicles.


C. Inhibition of both the dopamine transporter (DAT) and the norepinephrine transporter

(NET).


D. Antagonism at the alpha-2 adrenergic receptors in the prefrontal cortex.


Correct Answer: C


Explanation: Methylphenidate acts by blocking the reuptake of dopamine and

norepinephrine by inhibiting their respective transporters. Unlike amphetamines, it does

not significantly promote the release of dopamine from storage vesicles. This increase in

synaptic catecholamines in the prefrontal cortex helps improve attention and impulse

control.


2. A 72-year-old patient with Alzheimer’s disease is prescribed Donepezil. What is the most

common side effect the PMHNP should warn the caregiver about?

A. Hypertension

,B. Gastrointestinal distress including nausea and diarrhea


C. Urinary retention


D. Dry mouth and blurred vision


Correct Answer: B


Explanation: Donepezil is a cholinesterase inhibitor that increases acetylcholine levels,

which can lead to parasympathetic overstimulation. The most frequently reported adverse

effects involve the gastrointestinal system, such as nausea, vomiting, and diarrhea. These

symptoms are often dose-related and may improve over time or with a lower starting dose.


3. Which medication used for Medication-Assisted Treatment (MAT) of opioid use disorder

acts as a partial mu-opioid agonist?

A. Buprenorphine


B. Naltrexone


C. Methadone


D. Naloxone


Correct Answer: A


Explanation: Buprenorphine is a partial mu-opioid agonist that exhibits a ceiling effect,

reducing the risk of respiratory depression compared to full agonists. It has a high affinity

for the mu-receptor, meaning it can displace other opioids and potentially precipitate

,withdrawal if given too early. It is often combined with naloxone to prevent intravenous

misuse.


4. When prescribing Atomoxetine for ADHD, which Black Box Warning must the PMHNP

discuss with the patient and family?

A. Risk of Stevens-Johnson Syndrome


B. Potential for severe liver injury


C. High potential for abuse and physical dependence


D. Increased risk of suicidal ideation in children and adolescents


Correct Answer: D


Explanation: Atomoxetine carries a Black Box Warning regarding the increased risk of

suicidal ideation in pediatric patients. While liver injury is a rare potential side effect, it is

not the primary Black Box Warning focused on psychiatric monitoring. Providers must

regularly assess for changes in mood or behavior during the initial months of treatment.


5. Memantine (Namenda) is indicated for moderate to severe Alzheimer’s disease. What is its

unique mechanism of action?

A. Reversible inhibition of acetylcholinesterase


B. Potentiation of GABAergic neurotransmission


C. Uncompetitive NMDA receptor antagonism


D. Beta-amyloid plaque degradation

, Correct Answer: C


Explanation: Memantine acts as an NMDA receptor antagonist by binding to the

magnesium site when the channel is excessively open. This helps regulate glutamate

activity and prevents excitotoxicity which is thought to contribute to neuronal cell death in

Alzheimer’s. It is often used in combination with cholinesterase inhibitors for synergistic

effects.


6. A patient is being treated for alcohol use disorder with Disulfiram. What is the critical

mechanism behind the ‘disulfiram reaction’?

A. Inhibition of the enzyme aldehyde dehydrogenase


B. Blockade of opioid receptors leading to dysphoria


C. Rapid depletion of dopamine in the reward pathway


D. Competitive inhibition of alcohol dehydrogenase


Correct Answer: A


Explanation: Disulfiram inhibits aldehyde dehydrogenase, the enzyme responsible for

breaking down acetaldehyde, a toxic metabolite of alcohol. When alcohol is consumed,

acetaldehyde accumulates, causing severe physical reactions like flushing, nausea, and

tachycardia. This serves as a psychological deterrent rather than a physiological craving

reducer.


7. Which of the following stimulants is a prodrug intended to reduce the potential for abuse?

A. Vyvanse (Lisdexamfetamine)

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