欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Quintanrix
适用类别Human
治疗领域Hepatitis B;Tetanus;Immunization;Meningitis, Haemophilus;Whooping Cough;Diphtheria
通用名/非专利名称diphtheria, tetanus, pertussis (whole cell), hepatitis B (rDNA) and Haemophilus influenzae type B conjugate vaccine (absorbed)
活性成分Diphtheria toxoid;tetanus toxoid;inactivated Bordetella pertussis;hepatitis B surface antigen (rDNA);Haemophilus influenzae type b polysaccharide
产品号EMEA/H/C/000556
患者安全信息No
许可状态Withdrawn
ATC编码J07CA10
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2005/02/17
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2007/12/11
修订号2
治疗适应症Quintanrix is indicated for primary immunisation of infants (during the first year of life) against diphtheria, tetanus, pertussis, hepatitis B and invasive disease caused by Haemophilus influenzae type b and for booster immunisation of young children during the second year of life.The use of Quintanrix should be determined on the basis of official recommendations.
适用物种
兽用药物ATC编码
首次发布日期2007/12/11
最后更新日期2008/09/10
产品说明书https://www.ema.europa.eu/en/documents/product-information/quintanrix-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/quintanrix
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