欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Optaflu
适用类别Human
治疗领域Influenza, Human;Immunization
通用名/非专利名称influenza vaccine (surface antigen, inactivated, prepared in cell cultures)
活性成分influenza virus surface antigens (haemagglutinin and neuraminidase), inactivated, of the following strains:A/California/7/2009 (H1N1)pdm09 - like strain(A/Brisbane/10/2010, wild type)A/Switzerland/9715293/2013 (H3N2) - like strain(A/South Australia/55/2014, wild type)B/Phuket/3073/2013–like strain(B/Utah/9/2014, wild type)
产品号EMEA/H/C/000758
患者安全信息No
许可状态Expired
ATC编码J07BB02
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2007/06/01
上市许可开发者/申请人/持有人Seqirus GmbH
人用药物治疗学分组Vaccines
兽用药物治疗学分组
欧盟委员会决定日期2016/12/12
修订号16
治疗适应症Prophylaxis of influenza for adults, especially in those who run an increased risk of associated complications. Optaflu should be used in accordance to official guidance.
适用物种
兽用药物ATC编码
首次发布日期2016/12/12
最后更新日期2017/06/27
产品说明书https://www.ema.europa.eu/en/documents/product-information/optaflu-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/optaflu
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