التداخل بين فلوفوكسامين وتيربينافين

Drugs predominantly metabolized by the CYP450 2D6 isozyme include the following drug classes: tricyclic antidepressants, selective serotonin reuptake inhibitors, beta-blockers, antiarrhythmics class 1C (e.g., flecainide and propafenone) and monoamine oxidase inhibitors Type B.

In vitro data suggest that fluvoxamine is a relatively weak inhibitor of CYP2D6.