In 2009 the first case-control analysis to determine the odds of AED substitution among patients requiring emergency care was published in the journal Epilepsia (Zachry, et al). Using the Ingenix LabRX data base, the study reported that patients who had an epileptic event requiring emergency care, who had not required care for at least six months, had 81% greater odds of having an AED formulation switch.

The results of the Zachry study have been replicated using a different data base (PharMetrics) and an even larger control group. Published in the July 2009 issue of the journal Pharmacotherapy, Rascati and colleagues conclude: "Patients who had an epileptic event requiring acute care were about 80% more likely than matched controls without an acute event to have recently had an antiepileptic drug substitution. Replication of a previously published case-control analysis revealed a similar association between substitution involving A-rated antiepileptic drugs and subsequent epileptic events requiring acute care, thereby lending credibility to the findings."

Most recently, in an article titled "Antiepileptic drugs: the drawbacks of generic substitution," the journal The Lancet Neurology stated that "until firm evidence supporting the safety of generic switching becomes available, we should err on the side of caution and ensure that AEDs are excluded from any sweeping policies that promote automatic generic substitution."

In addition, the journal Neurology published a study by Labiner, et al., which found that with five common AEDs in the U.S., generic substitution was associated with significantly greater use of medical resources and risk of epilepsy-related medical events, compared to brand use.

Links to these articles, and others, appear below: