Abstract

Triptans generally have a low potential for drug interactions, with pharmacodynamic interactions likely to be of greater clinical significance than pharmacokinetic interactions. The most notable pharmacodynamic interactions include additive vasoconstrictor effects (e.g. with concomitant ergots) and serotonin syndrome (e.g. with concomitant selective serotonin reuptake inhibitors).

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call