التداخل بين فلوفوكسامين وكينيدين

Caution is indicated in patients known to have reduced levels of CYP2D6 activity and those receiving concomitant drugs known to inhibit this cytochrome P450 isoenzyme (e.g., quinidine).

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

Cytochrome P450 IID6 is an enzyme critical to the metabolism of many drugs, notably including mexiletine , some phenothiazines , and most polycyclic antidepressants .