Drug Interactions Flashcards
7 cards from real PSA practice questions. Tap to flip, then mark Knew It or Still Learning — missed cards come back until you master them.
Read the first 7 Drug Interactions flashcards as text
A patient stabilized on warfarin begins rifampicin for tuberculosis. What is the most likely effect on the INR?
Answer: INR decreases due to CYP2C9 induction by rifampicin
Rifampicin is a potent CYP2C9 inducer that accelerates warfarin metabolism, substantially reducing its anticoagulant effect and lowering the INR.
A patient on simvastatin 40 mg is prescribed clarithromycin for a respiratory infection. What is the primary risk?
Answer: Increased risk of myopathy or rhabdomyolysis due to elevated simvastatin levels
Clarithromycin potently inhibits CYP3A4, the primary enzyme metabolizing simvastatin, causing plasma accumulation and a significantly increased risk of muscle toxicity.
A patient receiving standard-dose codeine reports no pain relief. Which CYP enzyme variant most likely explains this pharmacogenomic interaction?
Answer: CYP2D6 poor metabolizer preventing conversion of codeine to morphine
CYP2D6 converts codeine to its active analgesic metabolite morphine; poor metabolizers (7–10% of Caucasians) derive minimal analgesia from codeine.
Fluoxetine (a potent CYP2D6 inhibitor) is started in a patient already taking tramadol. What is the most important risk?
Answer: Tramadol accumulation and serotonin syndrome risk due to CYP2D6 inhibition
Fluoxetine inhibits CYP2D6, which metabolizes tramadol to its active form; inhibition elevates parent tramadol levels and impairs serotonin reuptake clearance, raising serotonin syndrome risk.
A patient on combined oral contraceptives starts carbamazepine for epilepsy. What is the pharmacokinetic mechanism of concern?
Answer: CYP3A4 induction by carbamazepine reduces estrogen and progestogen plasma levels
Carbamazepine is a potent CYP3A4 inducer that accelerates hepatic metabolism of ethinylestradiol and progestogens, reducing contraceptive hormone levels and risking contraceptive failure.
Omeprazole co-prescription reduces the antiplatelet efficacy of clopidogrel. What is the mechanism?
Answer: CYP2C19 inhibition by omeprazole reduces conversion of clopidogrel to its active thiol metabolite
Clopidogrel is a prodrug requiring CYP2C19 for bioactivation; omeprazole inhibits this enzyme, reducing formation of the active metabolite and diminishing platelet P2Y12 inhibition.
A patient on long-term methadone maintenance is started on phenytoin for new-onset seizures. What is the anticipated outcome?
Answer: Opioid withdrawal symptoms from phenytoin-induced increase in methadone clearance
Phenytoin is a broad enzyme inducer (CYP3A4, CYP2C9) that significantly accelerates methadone metabolism, precipitating opioid withdrawal in dependent patients.