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The anticonvulsants, sometimes also called antiepileptics, belong to a diverse group of pharmaceuticals used in prevention of the occurrence of epileptic seizures. More and more, anticonvulsants are also finding ways into the treatment of bipolar disorder, since many appear to act as mood stabilizers. The goal of one anticonvulsant is to overpower the rapid and excessive firing of neurons that impulse a seizure. Failing this, a suitable anticonvulsant would impede the spread of the seizure inside the brain and offer protection in opposition to possible excitotoxic effects that may result in brain damage. in whatever manner, anticonvulsants themselves have been linked to lowered IQ and cell apoptosis.

Many anticonvulsants block Sodium (Na+) channels, Calcium (Ca2+) channels, AMPA receptors or NMDA receptors. Some anticonvulsants inhibit the metabolism of GABA or increase its release.

Some anticonvulsants require shown antiepileptogenic effects in animal models of epilepsy. That is, they either prevent the expected development of epilepsy or can halt or reverse the progress of epilepsy. However, no drug has shown this effect in human trials.

Approval

The usual course of achieving approval for a drug is to make known it is cogent at what time compared against placebo, or that it is more effective than an existing drug. In monotherapy (where only one drug is taken) it is not ethical to conduct a trial with placebo generic anti convulsants upon a new drug of uncertain efficacy. This is because untreated epilepsy foliage the patient at significant risk of dying. Therefore, almost all new epilepsy drugs are initially approved only as adjunctive (add-on) therapies. Patients who's epilepsy is publicly uncontrolled by their medication (i.e., it is stubborn to treatment) are selected to see if supplementing the medication with the new drug leads to an improvement in hold control. Any reduction in the frequency of seizures is compared against a placebo.

Once in that place is confidence that a drug is likely to subsist effective in monotherapy, trials are conducted where the drug is compared to some existing standard. For partial-onset seizures, this is typically carbamazepine. Despite the launch of over ten drugs since 1990, no starting anew drug has been shown to be more sufficient than the older harden, which includes carbamazepine, valproate and phenytoin. The lack of superiority extremely existing treatment, combined with the lack of placebo-controlled trials, means that few modern drugs have earned FDA approval as initial monotherapy. In striking difference, Europe only requires equivalence to existing treatments, and has approved various more. Despite their lack of FDA approval, the American Academy of Neurology and the American Epilepsy Society mute recommend a number of these new drugs as incipient monotherapy.

Drugs

In the following list, the dates in parentheses are the earliest approved use of the drug.

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