Topiramate is a structurally novel anti-epileptic drug with at least 3
postulated mechanisms of action including: 1) potentiation of GABA re
sponses, 2) impairment of AMPA/kainate glutamate receptors and 3) supp
ression of high frequency action potential firing. It has a favourable
pharmacokinetic profile with rapid absorption, good bio-availability,
linear pharmacokinetics, relatively long half-life and limited pharma
cokinetic drug interactions. However, topiramate. can reduce the estro
gen component of oral contraceptive medications. Women may require bir
th control preparations containing 50 mu g of estrogen. Topiramate cle
arance is reduced in severe renal failure and increased by enzyme-indu
cing antiepileptic drugs. The dose of topiramate may have to be reduce
d in renal failure or when withdrawing enzyme inducers.