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New antiepileptic drugs: review on drug interactions.

机译:新的抗癫痫药:药物相互作用综述。

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During the Past decade, nine new antiepileptic drugs (AEDs) namely, Felbamate, Gabapentin, Levetiracetam, Lamotrigine, Oxcarbazepine, Tiagabine, Topiramate, Vigabatrin and Zonisamide have been marketed worldwide. The introduction of these drugs increased appreciably the number of therapeutic combinations used in the treatment of epilepsy and with it, the risk of drug interactions. In general, these newer antiepileptic drugs exhibit a lower potential for drug interactions than the classic AEDs, like phenytoin, carbamazepine and valproic acid, mostly because of their pharmacokinetic characteristics. For example, vigabatrin, levetiracetam and gabapentin, exhibit few or no interactions with other AEDs. Felbamate, tiagabine, topiramate and zonisamide are sensitive to induction by known anticonvulsants with inducing effects but are less vulnerable to inhibition by common drug inhibitors. Felbamate, topiramate and oxcarbazepine are mild inducers and may affect the disposition of oral contraceptives with a risk of failure of contraception. These drugs also inhibit CYP2C19 and may affect the disposition of phenytoin. Lamotrigine is eliminated mostly by glucuronidation and is susceptible to inhibition by valproic acid and induction by classic AEDs such as phenytoin, carbamazepine, phenobarbital and primidone.
机译:在过去的十年中,已在全球范围内销售了9种新的抗癫痫药(AED),即非巴马特,加巴喷丁,左乙拉西坦,拉莫三嗪,奥卡西平,替加滨,托吡酯,维加巴特林和唑尼沙胺。这些药物的引入明显增加了用于治疗癫痫的治疗组合的数量,并由此增加了药物相互作用的风险。通常,这些新的抗癫痫药与苯乙妥英,卡马西平和丙戊酸等经典AED相比,具有较低的药物相互作用潜力,这主要是由于它们的药代动力学特性。例如,维加巴特林,左乙拉西坦和加巴喷丁与其他AED几乎没有相互作用。苯甲酸酯,替加滨,托吡酯和唑尼沙胺对已知抗惊厥药的诱导敏感,具有诱导作用,但较不易被普通药物抑制剂抑制。苯甲酸酯,托吡酯和奥卡西平是温和的诱导剂,可能会影响口服避孕药的处置,并可能导致避孕失败。这些药物还抑制CYP2C19并可能影响苯妥英的处置。拉莫三嗪主要通过葡萄糖醛酸化作用消除,并容易受到丙戊酸的抑制和经典AED(如苯妥英钠,卡马西平,苯巴比妥和primidone)的诱导。

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