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关于新型抗惊厥药奥卡西平的进一步临床及药代动力学观察

Further clinical and pharmacokinetic observations on the new anticonvulsant, oxcarbazepine.

作者信息

Dickinson R G, Hooper W D, Pendlebury S C, Moses D, Eadie M J

机构信息

Department of Medicine, University of Queensland.

出版信息

Clin Exp Neurol. 1988;25:127-33.

PMID:3077098
Abstract

Continuing experience with oxcarbazepine has shown that the drug tends to be less sedative than carbamazepine and at least as potent as an anticonvulsant but much more likely to cause hyponatraemia. The behaviour of the clearance of oxcarbazepine over a period of 3 months raises the possibility that the drug may not be as active an inducer of drug metabolism as is carbamazepine.

摘要

奥卡西平的持续应用经验表明,与卡马西平相比,该药的镇静作用往往较弱,作为抗惊厥药的效力至少相当,但更易导致低钠血症。奥卡西平在3个月期间的清除情况表明,该药作为药物代谢诱导剂的活性可能不如卡马西平。

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Anticonvulsants and breast feeding: a critical review.抗惊厥药与母乳喂养:一项批判性综述。
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Newer antiepileptic drugs. Towards an improved risk-benefit ratio.新型抗癫痫药物。旨在改善风险效益比。
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Oxcarbazepine. A review of its pharmacology and therapeutic potential in epilepsy, trigeminal neuralgia and affective disorders.奥卡西平。对其在癫痫、三叉神经痛和情感障碍方面的药理学及治疗潜力的综述。
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