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Withdrawal from antiepileptic drugs should be gradual to avoid the risk of precipitating rebound seizures. It is not known exactly how antiepileptic drugs work, but two mechanisms seem to be important for drugs in current use, while newer drugs may work by other means yet to be elucidated. Many well-established antiepileptic drugs (for example phenobarbital and benzodiaze pines) are known to facilitate the opening of GABA chloride ion channels at synapses. However, this is not the complete explanation as, for example phenobarbital is far more effective as an anticonvulsant than other barbiturates with the same enhancing effects on GABA. Newer drugs have been shown to interfere with GABA in other ways: by inhibiting GABA-transaminase, the enzyme responsible for inactivating GABA (vigabatrin and valproate) or by directly stimulating GABA receptors. Sodium ion channels in the neuronal membrane open during the depolarization phase of an action potential.

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A small amount of alcohol is excreted in this way but this accounts for only a small proportion of the overall elimination. Loss of drugs in sweat and breast milk occurs, but is of minor importance although the appearance of drugs in breast milk can have serious consequences for the nursing baby. Drugs can be administered to patients by a variety of routes and can be intended to have a local or systemic effect. The oral route is the most commonly used for systemic effect because it is convenient and generally acceptable to patients and requires no special skills.

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