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WGU D345/ D345 Psychopharmacology OA Exam (Latest 2026/2027 Update) | Complete Study Guide + Verified Q&A and Detailed Rationales | Neurotransmitters, Pharmacokinetics | A+ Graded

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INSTANT PDF DOWNLOAD – This comprehensive study guide is designed for the WGU D345 Psychopharmacology Objective Assessment (OA) (Latest 2026/2027 Update), featuring 150+ verified exam questions with correct answers and detailed rationales . This resource covers all key domains required to pass the OA, including foundational neuroscience, pharmacokinetics and pharmacodynamics, major drug classes (antidepressants, antipsychotics, anxiolytics, mood stabilizers), neurotransmitter systems, receptor pharmacology, and adverse effects. Key Topics & Practice Q&A Domain 1: Foundational Neuroscience & Pharmacokinetics Pharmacokinetics: What the body does to the drug—absorption, distribution, metabolism, and excretion (ADME) . Pharmacodynamics: What the drug does to the body—mechanism of action, receptor binding, and therapeutic effects . Acetylcholine: Synthesized in the basal nucleus of Meynert. Involved in learning, short-term memory, arousal, and reward. Low levels are associated with Alzheimer's disease; high levels with Parkinsonian symptoms . Serotonin (5-HT): Produced in the raphe nuclei of the brain stem. Implicated in mood, satiety, temperature, sleep, and pain sensitivity. Low levels are associated with depression, anxiety, OCD, and violence . Norepinephrine: Produced in the locus ceruleus of the pons. Involved in arousal, reward, and attention. Low levels are associated with depression; high levels with anxiety and the fight-or-flight response . Glutamate: A major excitatory neurotransmitter involved in memory. Increased levels are associated with anxiety; imbalances are implicated in mood disorders and schizophrenia . Steady State: Achieved after approximately 4-5 half-lives of a drug. For a drug with a 24-hour half-life, it takes 5-6 days . Partial Agonist: Binds to a receptor and produces a weaker biological response than a full agonist, acting as a "middle ground" between an agonist and an antagonist . CYP450 2D6: Metabolizes the majority of SSRIs, leading to significant potential for drug-drug interactions. Poor metabolizers are at higher risk for adverse effects . Domain 2: Antidepressants Bupropion (Wellbutrin): Least likely to cause sexual dysfunction among antidepressants. Also used for smoking cessation and ADHD. Lowers seizure threshold . SSRI Side Effects: Sexual dysfunction and GI upset (nausea, diarrhea) are common and affect adherence. Nausea usually subsides, but sexual dysfunction may persist . MAOI Caution: MAOIs inhibit monoamine oxidase, affecting dopamine, norepinephrine, and serotonin. Tyramine-rich foods (aged cheese, cured meats) must be avoided to prevent hypertensive crisis . Serotonin Syndrome: Characterized by "shits and shivers"—diarrhea, shivering, hyperreflexia, increased temperature, vital sign instability, and restlessness. Often caused by combining serotonergic agents (e.g., SSRIs + MAOIs) . Ketamine Mechanism: Noncompetitive NMDA receptor antagonist. Blocks NMDA receptors on GABAergic interneurons, disinhibiting glutamate release. Promotes synaptogenesis and neuroplasticity, producing rapid antidepressant effects within hours .

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Institution
NURS 6438 PSCHOPHARMACOLOGY
Course
NURS 6438 PSCHOPHARMACOLOGY

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WGU — D345 Pharmacology




MRAHP · 543D
WGU

D345 Psychopharmacology, Drug Reactions & Toxicology
PHARM A NEW KIND OF U — EVIDENCE-BASED PHARMACOLOGY



WGU D345 — Pharmacology: Psychopharmacology &
Drug Reactions
CO M P L E T E Q U E ST I O N S & V E R I F I E D A N S W E RS | 1 9 3 Q U E ST I O N S | CO M P R E H E N S I V E
EXAM REVIEW

INSTITUTION Western Governors University COURSE CODE D345 — Pharmacology
(WGU)
PROGRAM Nursing / Advanced Pharmacology ACADEMIC YEAR
EXAM TITLE WGU D345 — Pharmacology | TOTAL QUESTIONS 193 Questions
Complete Questions & Verified
Answers
COURSE TITLE Advanced Psychopharmacology & FORMAT Multiple Choice — Select the
Drug Reactions Single Best Answer


EXAMINATION INSTRUCTIONS
▸ Select the single best answer for each question.
▸ Questions cover DRESS/TEN/SJS, antipsychotics, mood stabilizers, anxiolytics, ADHD medications,
dementia treatments, substance abuse, and CYP450 interactions.
▸ Correct answers and detailed clinical rationales appear below each question.
▸ Content sourced from Stahl, Carlat, and evidence-based psychopharmacology guidelines. Verify all
dosages with current prescribing references.

, SECTION I — WGU D345 COMPREHENSIVE
Questions 1 – 193
PHARMACOLOGY EXAMINATION

1. What D2 occupancy is associated with antipsychotic efficacy?
A. Approximately 30%-50%
B. Approximately 60%-80%
C. Approximately 90%-100%
D. Approximately 10%-20%
CORRECT ANSWER B — Approximately 60%-80%
RATIONALE Antipsychotic efficacy correlates with striatal D2 receptor occupancy of
approximately 60-80%. Below 60% occupancy, antipsychotic effect is typically
insufficient. This therapeutic window was established through PET imaging
studies. Most antipsychotics achieve this range at standard therapeutic doses.
This is a high-yield D345 concept linking receptor pharmacology to clinical
response.

2. What happens when D2 occupancy exceeds 80%?
A. Antipsychotic efficacy improves dramatically without adverse effects
B. EPS and hyperprolactinemia become more likely
C. Negative symptoms of schizophrenia resolve completely
D. Cognitive function significantly improves
CORRECT ANSWER B — EPS and hyperprolactinemia become more likely
RATIONALE D2 occupancy exceeding 80% in the nigrostriatal pathway causes extrapyramidal
symptoms (EPS), while excessive blockade in the tuberoinfundibular pathway
elevates prolactin (hyperprolactinemia). This ceiling effect explains why higher
antipsychotic doses do not produce greater efficacy but significantly increase
adverse effects. The narrow therapeutic window of 60-80% D2 occupancy is a
fundamental concept in antipsychotic pharmacology.

,3. What are extrapyramidal symptoms (EPS)?
A. Metabolic side effects of antipsychotics
B. Movement disorders caused by dopamine blockade in the nigrostriatal pathway
C. Gastrointestinal effects of SSRIs
D. Cardiac conduction abnormalities
CORRECT ANSWER B — Movement disorders caused by dopamine blockade in the
nigrostriatal pathway
RATIONALE EPS are movement disorders resulting from antipsychotic blockade of dopamine
D2 receptors in the nigrostriatal pathway. This disrupts the normal balance
between dopamine and acetylcholine in the basal ganglia. The four major EPS
syndromes are acute dystonia, pseudoparkinsonism, akathisia, and tardive
dyskinesia. EPS are more common with high-potency first-generation
antipsychotics (haloperidol, fluphenazine).


4. What are the four major EPS syndromes?
A. Serotonin syndrome, NMS, anticholinergic toxicity, and lithium toxicity
B. Acute dystonia, pseudoparkinsonism, akathisia, and tardive dyskinesia
C. Agranulocytosis, myocarditis, seizures, and ileus
D. Weight gain, diabetes, hyperlipidemia, and hypertension
CORRECT ANSWER B — Acute dystonia, pseudoparkinsonism, akathisia, and tardive
dyskinesia
RATIONALE The four major EPS syndromes are: (1) Acute dystonia — sudden sustained
muscle contractions (hours to days); (2) Pseudoparkinsonism — tremor, rigidity,
bradykinesia (days to weeks); (3) Akathisia — inner restlessness with inability to
remain still; (4) Tardive dyskinesia — late-onset involuntary repetitive
movements (months to years, may be irreversible). This classification is high-
yield for D345 and all psychopharmacology examinations.

, 5. What is acute dystonia?
A. Gradual onset of tremor and rigidity over weeks
B. Sudden sustained muscle contractions causing abnormal postures
C. Inner restlessness with pacing
D. Late-onset oral-facial movements
CORRECT ANSWER B — Sudden sustained muscle contractions causing abnormal postures
RATIONALE Acute dystonia is characterized by sudden, sustained, painful muscle
contractions causing abnormal postures — often involving the neck (torticollis),
eyes (oculogyric crisis), tongue, jaw, or back. It typically occurs within hours to
days of initiating or increasing antipsychotic dose, more commonly in young
males and with high-potency FGAs. Treatment is anticholinergics (benztropine
or diphenhydramine), which provide rapid relief.


6. What is oculogyric crisis?
A. Uncontrollable blinking
B. Upward deviation of the eyes due to dystonia
C. Rapid eye movements during sleep
D. Double vision from anticholinergic effects
CORRECT ANSWER B — Upward deviation of the eyes due to dystonia
RATIONALE Oculogyric crisis is a classic acute dystonic reaction where the eyes deviate
upward (or occasionally laterally or downward) and are fixed in that position due
to sustained contraction of extraocular muscles. It is distressing and frightening
for patients. It responds rapidly to anticholinergic treatment (benztropine or
diphenhydramine). Recognition is critical — it may be mistaken for a psychiatric
or neurological emergency when it is actually a readily treatable medication side
effect.

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Course
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