This article surveys the pharmacokinetic parameters for the new antiep
ileptic drugs (AEDs): felbamate, gabapentin, lamotrigine, oxcarbazepin
e, tiagabine, topiramate, and vigabatrin. Compared to the pharmacokine
tics of standard AEDs, these new AEDs have progressed in terms of (a)
longer half-lives, permitting once- or twice-daily dosing, (b) greatly
reduced potential for drug interactions, thus increasing ease of trea
tment, and (c) general lack of hepatic enzyme induction, which facilit
ates polytherapy as well as other aspects of treatment.