欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Daronrix
适用类别Human
治疗领域Influenza, Human; Immunization; Disease Outbreaks
通用名/非专利名称pandemic influenza vaccine (whole virion, inactivated, adjuvanted)
活性成分Whole virion, inactivated, containing antigen*: A/Vietnam/1194/2004 (H5N1)* produced in eggs
产品号EMEA/H/C/000706
患者安全信息no
授权状态Withdrawn
ATC编码J07BB01
是否额外监管no
是否仿制药no
是否生物类似药no
是否附条件批准no
是否特殊情形yes
是否加速审评no
是否罕用药no
批准上市日期2007/03/21
上市许可持有人/公司名称GlaxoSmithKline Biologicals S.A.
人用药物治疗分组Vaccines
决定日期2007/03/21
修订号0
适应症Prophylaxis of influenza in an officially declared pandemic situation. Pandemic influenza vaccine should be used in accordance with official guidance.
首次发布日期2007/03/21
修订日期2013/07/02
产品信息https://www.ema.europa.eu/en/documents/product-information/daronrix-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/daronrix
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