欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Ribavirin BioPartners
适用类别Human
治疗领域Hepatitis C, Chronic
通用名/非专利名称ribavirin
活性成分ribavirin
产品号EMEA/H/C/001184
患者安全信息No
许可状态Lapsed
ATC编码J05AB04
是否额外监管No
是否仿制药或hybrid药物Yes
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2010/04/06
上市许可开发者/申请人/持有人BioPartners GmbH
人用药物治疗学分组Antivirals for systemic use
兽用药物治疗学分组
欧盟委员会决定日期2012/11/21
修订号2
治疗适应症Ribavirin BioPartners is indicated for the treatment of chronic hepatitis-C-virus (HCV) infection in adults, children three years of age and older and adolescents and must only be used as part of a combination regimen with interferon alfa-2b. Ribavirin monotherapy must not be used. There is no safety or efficacy information on the use of ribavirin with other forms of interferon (i.e. not alfa-2b). Naïve patients Adult patients Ribavirin BioPartners is indicated, in combination with interferon alfa-2b, for the treatment of adult patients with all types of chronic hepatitis C except genotype 1, not previously treated, without liver decompensation, with elevated alanine aminotransferase (ALT), who are positive for hepatitis C viral ribonucleic acid (HCV-RNA) (see section 4.4) Children three years of age and older and adolescents Ribavirin BioPartners is intended for use, in a combination regimen with interferon alfa-2b, for the treatment of children three years of age and older and adolescents, who have all types of chronic hepatitis C except genotype 1, not previously treated, without liver decompensation, and who are positive for HCV-RNA. When deciding to not to defer treatment until adulthood, it is important to consider that the combination therapy induced a growth inhibition. The reversibility of growth inhibition is uncertain. The decision to treat should be made on a case by case basis (see section 4.4). Previous-treatment-failure patients Adult patients Ribavirin BioPartners is indicated, in combination with interferon alfa-2b, for the treatment of adult patients with chronic hepatitis C who have previously responded (with normalisation of ALT at the end of treatment) to interferon alfa monotherapy but who have subsequently relapsed (see section 5.1).
适用物种
兽用药物ATC编码
首次发布日期2012/11/21
最后更新日期2013/05/06
产品说明书https://www.ema.europa.eu/en/documents/product-information/ribavirin-biopartners-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/ribavirin-biopartners
©2006-2025 DrugFuture->European Medicines Agency Authorisation of Medicines DataBase