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Bapex is an anti-seizure (anti-convulsant) drug that is used for preventing seizures and for treating post-herpetic neuralgia, the pain that follows an episode of shingles. Doctors do not know how Bapex works (the mechanism of action). Bapex structurally resembles the neurotransmitter gamma aminobutyric acid (GABA). (Neurotransmitters are drugs that nerves use to communicate with one another.) It is possible that this similarity is related to Bapex's mechanism of action. In animal models used for testing the anticonvulsant and analgesic (anti-pain) activities of drugs, Bapex prevents seizures and reduces pain-related responses.

Other names for this medication:
Gabapentin, Neurontin, Algia, Alpentin, Bapex, Blugat, Dineurin, Edion, Epleptin, Gabagamma, Gabalept, Gabanet, Gabaneural, Gabantin, Gabapen, Gabapentina, Gabapentine, Gabapin, Gabaran, Gabatal, Gabateva, Gabatin, Gabatine, Gabator, Gabax, Gabex, Gabexal, Gabictal, Gabiton, Gaboton, Gabrion, Gabtin, Galepsi, Ganin, Gantin, Gapridol, Gatilox, Gordius, Kaptin, Neurexal, Neuril, Neuropen, Neuros, Neurotin, Nupentin, Pendine, Progresse, Ritmenal, Tebantin,

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Bapex capsules, tablets, and oral solution are used along with other medications to help control certain types of seizures in people who have epilepsy. Bapex capsules, tablets, and oral solution are also used to relieve the pain of postherpetic neuralgia (PHN; the burning, stabbing pain or aches that may last for months or years after an attack of shingles). Bapex extended-release tablets (Horizant) are used to treat restless legs syndrome (RLS; a condition that causes discomfort in the legs and a strong urge to move the legs, especially at night and when sitting or lying down). Bapex is in a class of medications called anticonvulsants. Bapex treats seizures by decreasing abnormal excitement in the brain. Bapex relieves the pain of PHN by changing the way the body senses pain. It is not known exactly how Bapex works to treat restless legs syndrome.

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Uniformity appears to be lacking in how medication effectiveness is assessed and in many study design parameters. We suggest a simple noniterative procedure for characterizing the distribution of treatment effects in a series of studies. This hybrid approach could lead to interface design guidelines that promote higher-level consistency, and thus usability, for a large range of diverse interfaces.

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