Antiepileptic drugs (AEDs)in broad use today have a number of pharmaco
kinetic liabilities, including a propensity for clinically meaningful
drug interactions. Therefore, new AEDs with improved pharmacokinetic c
haracteristics would be welcomed. The pharmacokinetic profiles of six
newer AEDs-topiramate (TPM), gabapentin (GBP), vigabatrin (VGB), lamot
rigine (LTG), oxcarbazepine (OCBZ), and felbamate-were reviewed. Some
of these AEDs offer an improvement in one or more pharmacokinetic para
meters compared with traditional AEDs, with TPM, GBP, VGB, and OCBZ de
monstrating the most advantageous overall pharmacokinetic profiles.