2002
DOI: 10.1046/j.1365-2710.2002.00441.x
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Effect of vigabatrin on the pharmacokinetics of carbamazepine

Abstract: Vigabatrin produced a statistically significant increase in the plasma clearance of carbamazepine when the two drugs were given simultaneously.

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Cited by 16 publications
(3 citation statements)
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References 7 publications
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“…VB mainly relies on renal elimination and it does not need binding plasma proteins [192] or metabolism [193]. When patients with epilepsy were co-treated VB with other AEDs, VB might cause a significant increase in plasma clearance of CBZ [194] and decrease in the serum PT concentration [195]. VB is effective in the treatment of pediatric patients with infantile spasms, infantile spasms secondary to tuberous sclerosis, refractory complex partial seizures, and adult patients with LGS [196].…”
Section: New Generation Aedsmentioning
confidence: 99%
“…VB mainly relies on renal elimination and it does not need binding plasma proteins [192] or metabolism [193]. When patients with epilepsy were co-treated VB with other AEDs, VB might cause a significant increase in plasma clearance of CBZ [194] and decrease in the serum PT concentration [195]. VB is effective in the treatment of pediatric patients with infantile spasms, infantile spasms secondary to tuberous sclerosis, refractory complex partial seizures, and adult patients with LGS [196].…”
Section: New Generation Aedsmentioning
confidence: 99%
“…Mono-therapeutic treatment of epilepsy using a conventional antiepileptic drug carbamazepine has been reported to have prominent adverse effects especially on testicular functions (13). Vigabatrin is a newer antiepileptic which is used as an adjunct therapy in the treatment of epilepsy (14). However, reports on the combination of these drugs on reproductive functions have not been reported and need to be investigated, hence this study.…”
Section: Introductionmentioning
confidence: 99%
“…VGB is usually administered at doses ranging from 1.5 to 4 g/day [4]; it is well absorbed after an oral dose and its half-life time is about 5-8 h [5]. Plasma levels at steady-state are in the 10-100 mg/mL range, with the most frequent concentrations in the 20-60 mg/mL range [6]. About 50% of the patients experience adverse effects when treated with VGB.…”
Section: Introductionmentioning
confidence: 99%