ALABAMA
NU 578 UNIT 2 EXAM UNIVERSITY OF SOUTH
ALABAMA
NU 578 UNIT 2 EXAM UNIVERSITY OF SOUTH
ALABAMA
EXAM COVERAGE
1. Controlled Substances & DEA Schedules — DEA schedule definitions,
prescribing regulations, refill rules, and federal requirements for Schedule II–V
medications.
,2. Opioid Analgesics & Antagonists — Full agonists, partial agonists, mixed
agonist-antagonists, tramadol, and opioid antagonists including naloxone and
naltrexone.
3. Parkinson's Disease Pharmacotherapy — Levodopa/carbidopa, dopamine
agonists, MAO-B inhibitors, COMT inhibitors, amantadine, and management of
motor fluctuations.
4. Migraine & Headache Management — Triptans, ergotamines, prophylactic
agents including beta-blockers, anticonvulsants, and tricyclic antidepressants.
5. Antipsychotics & Lithium — First-generation vs. second-generation
antipsychotics, extrapyramidal symptoms, tardive dyskinesia, neuroleptic
malignant syndrome, and lithium monitoring.
6. Antidepressants — SSRIs, SNRIs, TCAs, MAOIs, mechanism of action, side
effects, and serotonin syndrome risk.
7. Benzodiazepines & Sedative-Hypnotics — Flumazenil, zolpidem, ramelteon,
barbiturates, and reversal agents.
, 8. CNS Stimulants & ADHD — Methylphenidate formulations, amphetamines,
side effects, and monitoring parameters.
9. Anxiety Disorders — Buspirone, benzodiazepines, and non-controlled
treatment options.
10. Drug Interactions & CYP450 — Warfarin interactions, CYP2C19 and
clopidogrel, and metabolic considerations in special populations.
NU 578 UNIT 2 EXAM UNIVERSITY OF SOUTH
ALABAMA
200 EXAM QUESTIONS WITH ANSWER RATIONALES
Question 1
, A patient currently maintained on buprenorphine/naloxone for opioid use
disorder is scheduled for an upcoming surgical procedure requiring acute pain
management. Which pharmacodynamic property of buprenorphine best explains
why standard full mu-opioid agonist dosing may fail to produce adequate
analgesia in this patient?
A. High intrinsic efficacy at the mu-opioid receptor
B. Partial agonist activity with ceiling effect at the mu-opioid receptor
C. Competitive antagonism at the kappa-opioid receptor
D. Irreversible inhibition of CYP3A4 metabolic pathways
Correct Answer: B
Explanation:
B: Buprenorphine is a partial agonist at the mu-opioid receptor, producing
submaximal effects and demonstrating a ceiling effect on respiratory
depression and analgesia. Because it occupies mu receptors with high affinity
but low intrinsic activity, full agonists like morphine or hydromorphone may be