Vigabatrin (VGB) is a recently-released antiepileptic drug which works
by a clearly-defined mechanism of action: inhibition of GABA transami
nase leading to an elevation of brain GABA concentration. It has been
proven effective, mainly as an add-on agent, in complex partial and se
condarily generalized seizures in both adults and children as well as
in infantile spasms in both short and long-term controlled studies. Wo
rld-wide experience now includes over 150,000 patients exposed to the
drug. VGB has a favorable pharmacokinetic profile since it has little
protein-binding, is mainly excreted unchanged by the kidney and has a
long effective half-life allowing once or twice daily dosing. It is ge
nerally well-tolerated with very few cognitive effects but may cause s
ignificant behavioral side effects such as agitation, irritability, de
pression or psychosis in approximately 2-4% of cases. Mild weight gain
and possible exacerbation of absence and myoclonic seizures are other
reported adverse effects. The role of VGB in other childhood epilepti
c syndromes apart from West syndrome is still being defined.