The incidence of psychosis during clinical trials of topiramate was 0.8%, n
ot significantly different from the rate for placebo or reported rates of p
sychosis in patients with refractory epilepsy. We observed psychotic sympto
ms in five patients soon after initiation of topiramate therapy. We perform
ed a retrospective chart review of the first 80 patients who began on topir
amate after approval for clinical use, between January and April 1997. Symp
toms suggestive of psychosis, including hallucinations and delusions, were
sought for analysis. Cognitive effects such as psychomotor slowing, confusi
on, and somnolence were not included. Five patients developed definite psyc
hotic symptoms 2 to 46 days after beginning topiramate. Dosages at symptom
onset were 50-400 mg/day. Symptoms included paranoid delusions in four pati
ents and auditory hallucinations in three. Symptoms of psychosis and other
psychiatric symptoms resolved quickly with discontinuation of topiramate in
three patients, dose reduction from 300 to 200 mg/day in one and with inpa
tient treatment and neuroleptics in another. One patient had a history of a
uditory hallucinations, one of aggressive and suicidal thoughts, but three
had no significant psychiatric history. Physicians should be aware of the p
ossibility of psychotic symptoms, even in patients without a previous psych
iatric history, when prescribing topiramate. Symptoms resolve quickly with
discontinuation.