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扎来普隆的安全性

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摘要 扎来普隆是γ-氨基丁酸A受体α1亚单位上的苯二氮?受体特异性激动剂,由于半衰期仅1小时,故服药4小时后对精神运动性操作无影响,次日无思睡,停药后反跳和撤药症状危险性小,但滥用危险性与三唑仑相同,扎来普隆与利福平联用时需增量,与酮康唑、红霉素和西咪替丁联用时需减量。
作者 徐捷
出处 《国际精神病学杂志》 2010年第1期50-54,共5页 Journal Of International Psychiatry
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