LEVEL 4 N03AG04

Δραστικές

Φάρμακα

  • DRUGBANK - Vigabatrin
  • indication:

    For use as an adjunctive treatment (with other drugs) in treatment resistant epilepsy, complex partial seizures, secondary generalized seizures, and for monotherapy use in infantile spasms in West syndrome.

  • pharmacology:

  • mechanism:

    It is believed that vigabatrin increases brain concentrations of gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter in the CNS, by irreversibly inhibiting enzymes that catabolize GABA (gamma-aminobutyric acid transaminase GABA-T) or block the reuptake of GABA into glia and nerve endings. Vigabatrin may also work by suppressing repetitive neuronal firing through inhibition of voltage-sensitive sodium channels.

  • toxicity:

  • absorprion:

    Rapidly absorbed following oral administration. Food may slightly decrease the rate, but not the extent, of absorption.

  • halflife:

    5-8 hours in young adults, 12-13 hours in elderly.

  • roouteelimination:

    Vigabatrin is not significantly metabolized; it is eliminated primarily through renal excretion.

  • volumedistribution:

    * 1.1 L/kg

  • clearance:

    * 2.4 +/- 0.8 L/h [Infant] * 5.7 +/- 2.5 L/h [Children]