法规知识库 · EMA 集中审评
Ribavirin Mylan (previously Ribavirin Three Rivers)
ribavirin · EMEA/H/C/001185 · 已撤市
获批上市许可
2010-06-10
欧委会决定日
2019-03-13
持有人 / 申请人
Mylan S.A.S
终止日期字段
无
从产品到官方文件
文件记录
6
官方索引 6
EPAR / 审评
4
assessment / overview 等
产品信息
2
PI / presentations
其他
0
RMP / PIP 等
ATC:J05AB04
治疗领域:Hepatitis C, Chronic
药理分类:Antivirals for systemic use
修订号:10 · 最新影响 PI 的程序:N/0030
适应症(原文):Ribavirin Mylan is indicated for the treatment of chronic hepatitis C and must only be used as part of a combination regimen with interferon alfa-2b (adults, children (three years of age and older) and adolescents). 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). Please refer also to the interferon alfa-2b summary of product characteristics (SmPC) for prescribing information particular to that product. Naïve patients Adult patients Ribavirin Mylan 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 serum hepatitis-C-virus (HCV) RNA. Children and adolescents Ribavirin Mylan is indicated, in a combination regimen with interferon alfa-2b, for the treatment of children and adolescents three years of age and older, who have all types of chronic hepatitis C except genotype 1, not previously treated, without liver decompensation, and who are positive for serum 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). Previously treatment-failure patients Adult patients Ribavirin Mylan 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 alpha monotherapy but who have subsequently relapsed.
关键日期时间轴
来自 EMA medicines JSON 日期字段;缺失字段不展示,不补推结论。
2019-03-13 · 欧委会决定
2010-06-10 · 获批上市许可
说明书、EPAR 与其他文件
仅展示 EMA 官方 document_url;本站不下载或镜像 PDF。
EPAR / 审评资料
- 打开官方文件 ↗
Ribavirin Mylan : EPAR - Procedural steps taken and scientific information after authorisation
procedural-steps-after · 2019-07-31
- 打开官方文件 ↗
Ribavirin Mylan-H-C-1185-PSUSA-10007-201307 : EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation
scientific-conclusion · 2014-06-19 · EMA/CHMP/318854/2014
- 打开官方文件 ↗
Ribavirin Mylan: EPAR - Summary for the public
overview · 2011-02-17
- 打开官方文件 ↗
Ribavirin Three Rivers : EPAR - Public assessment report
assessment-report · 2010-07-02
数据来自 EMA 官方 JSON;最终以 EMA / 欧委会文件为准。本页不自动给出安全或非安全结论。