欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Synflorix
适用类别Human
治疗领域Pneumococcal Infections;Immunization
通用名/非专利名称pneumococcal polysaccharide conjugate vaccine (adsorbed)
活性成分Pneumococcal polysaccharide serotype 23F;Pneumococcal polysaccharide serotype 4;Pneumococcal polysaccharide serotype 5;Pneumococcal polysaccharide serotype 6B;Pneumococcal polysaccharide serotype 7F;Pneumococcal polysaccharide serotype 9V;Pneumococcal polysaccharide serotype 1;Pneumococcal polysaccharide serotype 14;Pneumococcal polysaccharide serotype 18C;Pneumococcal polysaccharide serotype 19F
产品号EMEA/H/C/000973
患者安全信息No
许可状态Authorised
ATC编码J07AL52
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2009/03/29
上市许可开发者/申请人/持有人GlaxoSmithKline Biologicals S.A.
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2023/04/26
修订号36
治疗适应症Active immunisation against invasive disease and acute otitis media caused by Streptococcus pneumoniae in infants and children from six weeks up to five years of age. See sections 4.4 and 5.1 in product information for information on protection against specific pneumococcal serotypes. The use of Synflorix should be determined on the basis of official recommendations taking into consideration the impact of invasive disease in different age groups as well as the variability of serotype epidemiology in different geographical areas.
适用物种
兽用药物ATC编码
首次发布日期2017/10/12
最后更新日期2023/05/24
产品说明书https://www.ema.europa.eu/en/documents/product-information/synflorix-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/synflorix
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