Clinical Pharmacology & Therapeutics · 2006 · 11 citations · 12 references
MedicinePharmacokineticsPharmacologyBiochemical PharmacologyClinical PharmacologyHepatic PharmacokineticsCytochrome P450 EnzymesCytochrome P450 InteractionsCytochrome P450-mediated MetabolismDrug DispositionHepatic Drug MetabolismPsychotropic Drug InteractionsCyp2d6 Drug MetabolismCyp450-mediated InteractionsCytochrome P450 2D6Cytochrome P450 Enzyme InhibitionHepatic Drug InteractionsLife-threatening ArrhythmiasMetabolic Enzyme InhibitionPostoperative Dizziness
Pharmacokinetic studies demonstrate that propoxyphene is a potent inhibitor of cytochrome P450 (CYP) 2D6. Clinically significant sequelae have not been previously reported. We report a case of this inhibition manifested by life-threatening bradycardia in a patient receiving a CYP2D6 substrate, metoprolol. A 48-year-old man came to the emergency department complaining of dizziness 3 hours after ingesting metoprolol, at his usual dose, and 2 tablets of propoxyphene, newly begun postoperatively. Four hours after ingestion of both drugs, the patient was noted to have a ventricular rate of about 30 beats/min with underlying atrial fibrillation. The patient's ventricular response returned to normal within 11 hours of ingestion. We have demonstrated the clinical importance of the interaction between propoxyphene and metoprolol likely resulting from inhibition of hepatic clearance of metoprolol by propoxyphene. Underscoring the clinical relevance of CYP2D6 inhibition by an analgesic of questionable efficacy should proscribe its use.
12