In placebo-controlled trials, the overall incidence of nonconvulsive status
epilepticus was no higher in the tiagabine-treated group than in the place
bo-group. Case reports of nonconvulsive status epilepticus under tiagabine
suggested a specific role of dose levels, since in these patients symptoms
occurred mostly at 40 mg/day or higher. We report a case of complex partial
status epilepticus in a patient receiving a low dose of tiagabine and revi
ew all 11 case reports of nonconvulsive status epilepticus in patients on t
iagabine, with regard to daily doses. Our analysis suggests an individual r
isk threshold of unknown aetiology.