欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Matever
适用类别Human
治疗领域Epilepsy
通用名/非专利名称levetiracetam
活性成分levetiracetam
产品号EMEA/H/C/002024
患者安全信息No
许可状态Authorised
ATC编码N03AX14
是否额外监管No
是否仿制药或hybrid药物Yes
是否生物类似药No
是否附条件批准No
是否特殊情形No
是否加速审评No
是否罕用药No
上市许可日期2011/10/03
上市许可开发者/申请人/持有人Pharmathen S.A.
人用药物治疗学分组Antiepileptics
兽用药物治疗学分组
欧盟委员会决定日期2025/05/16
修订号28
治疗适应症Matever is indicated as monotherapy in the treatment of partial-onset seizures with or without secondary generalisation in patients from 16 years of age with newly diagnosed epilepsy. Matever is indicated as adjunctive therapy: in the treatment of partial-onset seizures with or without secondary generalisation in adults, children and infants from one month of age with epilepsy; in the treatment of myoclonic seizures in adults and adolescents from 12 years of age with juvenile myoclonic epilepsy; in the treatment of primary generalised tonic-clonic seizures in adults and adolescents from 12 years of age with idiopathic generalised epilepsy.
适用物种
兽用药物ATC编码
首次发布日期2018/07/02
最后更新日期2025/05/16
产品说明书https://www.ema.europa.eu/en/documents/product-information/matever-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/matever
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