欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Zyprexa Velotab
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/000287
患者安全信息No
许可状态Authorised
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2000/02/03
上市许可开发者/申请人/持有人CHEPLAPHARM Registration GmbH
人用药物治疗学分组Psycholeptics
兽用药物治疗学分组
审评意见日期1999/10/21
欧盟委员会决定日期2024/12/16
修订号34
治疗适应症Adults 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. In patients whose manic episode has responded to olanzapine treatment, olanzapine is indicated for the prevention of recurrence in patients with bipolar disorder.
适用物种
兽用药物ATC编码
首次发布日期2017/02/23
最后更新日期2024/12/18
产品说明书https://www.ema.europa.eu/en/documents/product-information/zyprexa-velotab-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/zyprexa-velotab
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