Polytherapy is often used in clinical practice. The drug associations
may lead to pharmacokinetic and/or pharmacodynamic interactions, with
clinical implications. The authors reported a quantified illustration
of 2 types of interactions in a depressed patient : between antidepres
sants, amitriptyline and fluoxetine, between these antidepressants and
antituberculosis. Firstly, when fluoxetine was added to amiptriptylin
e, it was observed, as expected, an increase of the tricyclic and its
metabolite plasma levels, despite a decrease of its dosage. Secondly,
when antituberculosis were added to the 2 antidepressants, it was obse
rved a decrease of the tricyclic drug plasma levels. These levels rema
ined below the therapeutic window even when the tricyclic antidepressa
nt dosage was increased. It seems that the fluoxetine interaction disa
ppeared. The competition between the inhibitory effect of fluoxetine a
nd the induction of rifampicin, on the metabolism of amitriptyline is
discussed.