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gamma-Vinyl GABA - General Information: An analogue of gamma-aminobutyric acid. It is an irreversible inhibitor of 4-aminobutyrate transaminase, the enzyme responsible for the catabolism of gamma-aminobutyric acid. (From Martindale The Extra Pharmacopoeia, 31st ed) Pharmacology: gamma-Vinyl GABA, is an anticonvulsant chemically unrelated to other anticonvulsants. gamma-Vinyl GABA inhibits the catabolism of GABA. It is an analog of GABA, but it is not a receptor agonist. gamma-Vinyl GABA for patients This medicine may reduce your ability to drive or operate machinery safely. Do not drive or operate machinery until you know how this medicine affects you and you are sure it won't affect your performance. Avoid stopping this medicine suddenly. The dose of this medicine should be gradually decreased over a period of two to four weeks. After months to years of taking this medication, damage to vision may occur. Regular eye examinations should be conducted and notify your doctor if any change in vision occurs. gamma-Vinyl GABA Interactions A study published in 2002 found that vigabatrin causes a statistically significant increase in plasma clearance of carbamazepine. In 1984, Drs Rimmer and Richens at the University of Wales reported that administering vigabatrin with phenytoin lowered the serum phenytoin concentration in patients with treatment-resistant epilepsy. The concentration of phenytoin falls to 23% within five weeks, according to an experiment published in 1989 by the same two scientists that tried and failed to elucidate the mechanism behind this interaction. gamma-Vinyl GABA Contraindications In pregnancy and lactation and in patients with a known hypersensitivity to vigabatrin or to any components of the product. Additional information about gamma-Vinyl GABAgamma-Vinyl GABA 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. Mechanism Of Action: 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. gamma-Vinyl GABA may also work by suppressing repetitive neuronal firing through inhibition of voltage-sensitive sodium channels. Drug Interactions: Not Available Food Interactions: Not Available Generic Name: Vigabatrin Synonyms: Not Available Where to order Vigabatrin (and gamma-Vinyl GABA analogs) online: Drug Category: Anticonvulsants; Enzyme Inhibitors Drug Type: Small Molecule; Approved Other Brand Names containing Vigabatrin: 4-Amino-5-hexenoic acid; 4-Aminohexenoic acid; GVG; Sabril (TN); Vigabatrin [USAN:BAN:INN]; Vigabatrina [Spanish]; Vigabatrine; Vigabatrine [French]; Vigabatrinum [Latin]; gamma-Vinyl GABA; Absorption: Rapidly absorbed following oral administration. Food may slightly decrease the rate, but not the extent, of absorption. Toxicity (Overdose): Not Available Protein Binding: Little to none Biotransformation: Almost no metabolic transformation. Does not induce the hepatic cytochrome P450 system. Half Life: 5-8 hours in young adults, 12-13 hours in elderly. Dosage Forms of gamma-Vinyl GABA: Tablet OralPowder Oral Chemical IUPAC Name: 4-aminohex-5-enoic acid Chemical Formula: C6H11NO2 Vigabatrin on Wikipedia: http://en.wikipedia.org/wiki/Vigabatrin Organisms Affected: Humans and other mammals
This medicine may reduce your ability to drive or operate machinery safely. Do not drive or operate machinery until you know how this medicine affects you and you are sure it won't affect your performance. Avoid stopping this medicine suddenly. The dose of this medicine should be gradually decreased over a period of two to four weeks. After months to years of taking this medication, damage to vision may occur. Regular eye examinations should be conducted and notify your doctor if any change in vision occurs.
A study published in 2002 found that vigabatrin causes a statistically significant increase in plasma clearance of carbamazepine. In 1984, Drs Rimmer and Richens at the University of Wales reported that administering vigabatrin with phenytoin lowered the serum phenytoin concentration in patients with treatment-resistant epilepsy. The concentration of phenytoin falls to 23% within five weeks, according to an experiment published in 1989 by the same two scientists that tried and failed to elucidate the mechanism behind this interaction.
In pregnancy and lactation and in patients with a known hypersensitivity to vigabatrin or to any components of the product.
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