Behavioural disturbances and psychotic reactions are commoner in patie
nts with epilepsy than in the general population and may be precipitat
ed by the majority of antiepileptic drugs, including the newer ones. T
hese reactions may be more frequent in patients with complex partial s
eizures, reflecting underlying temporal lobe pathology. A review of th
e literature on vigabatrin found an incidence of severe abnormal behav
iour in controlled trials in adults of 3.4%. In children open studies
gave an incidence of around 6%. This may be related to dosage and spee
d of introduction. Such reactions may be related to changes in seizure
central, either unaccustomed good control (forced normalisation) or b
reakdown in control, implying non-specific causative mechanisms. Alter
natively, any relationship to control may be fortuitous and specific,
unknown pharmacological mechanisms may be involved. Appropriate risk r
eduction measures include slow introduction, limiting the dose to that
required for seizure control, slow withdrawal and increased vigilance
in those on polytherapy or with psychiatric histories. Such advice is
pertinent to all antiepileptic medications. Additionally, vigabatrin
is probably contraindicated in idiopathic generalised epilepsies. Beha
vioural reactions are uncommon with vigabatrin, and have not been show
n to be greater with it than with other antiepileptic agents. Therefor
e, it maybe inappropriate to withhold the drug from those who may bene
fit from it.