欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Olansek
适用类别Human
治疗领域Schizophrenia;Bipolar Disorder
通用名/非专利名称olanzapine
活性成分olanzapine
产品号EMEA/H/C/000114
患者安全信息No
许可状态Withdrawn
ATC编码N05AH03
是否额外监管No
是否仿制药或hybrid药物No
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1996/10/07
上市许可开发者/申请人/持有人Eli Lilly Co. Ltd.
人用药物治疗学分组Psycholeptics
兽用药物治疗学分组
欧盟委员会决定日期2003/03/17
修订号
治疗适应症Olanzapine is indicated for the treatment of schizophrenia.Olanzapine is effective in maintaining the clinical improvement during continuation therapy in patients who have shown an initial treatment response.Olanzapine is indicated for the treatment of moderate to severe manic episode. Olanzapine has not been demonstrated to prevent recurrence of manic or depressive episodes (see Section 5.1).
适用物种
兽用药物ATC编码
首次发布日期2003/03/17
最后更新日期2003/06/12
产品说明书
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/olansek
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