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Psychiatry · Psychopharmacology: CYP interactions
Sample itemFluoxetine and paroxetine can raise plasma levels of many tricyclics and impair activation of prodrugs such as codeine and tamoxifen, by inhibiting which enzyme?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
C. CYP2D6
Fluoxetine and paroxetine are strong CYP2D6 inhibitors, which raises levels of TCAs, antipsychotics and some beta blockers, and reduces activation of prodrugs like codeine and tamoxifen. Fluoxetine's long half-life prolongs the effect.
Option by option
A. CYP1A2
CYP1A2 inhibition is characteristic of fluvoxamine.
B. CYP2E1
CYP2E1 is mainly relevant to alcohol and paracetamol.
C. CYP2D6 (correct)
Correct. CYP2D6 inhibition underlies the interaction.
D. CYP3A4 induction
Induction of CYP3A4 is typical of carbamazepine, not these SSRIs.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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