法规知识库 · EMA 集中审评
Tenofovir disoproxil Viatris (previously Tenofovir disoproxil Mylan)
tenofovir disoproxil · EMEA/H/C/004049 · 已授权
获批上市许可
2016-12-08
欧委会决定日
2026-06-26
持有人 / 申请人
Viatris Limited
终止日期字段
无
从产品到官方文件
文件记录
9
官方索引 9
EPAR / 审评
6
assessment / overview 等
产品信息
3
PI / presentations
其他
0
RMP / PIP 等
ATC:J05AF07
治疗领域:HIV Infections
药理分类:Antivirals for systemic use
修订号:25 · 最新影响 PI 的程序:VR/0000350382
适应症(原文):HIV-1 infection Tenofovir disoproxil 245 mg film-coated tablets are indicated in combination with other antiretroviral medicinal products for the treatment of HIV-1 infected adults. In adults, the demonstration of the benefit of tenofovir disoproxil in HIV-1 infection is based on results of one study in treatment-naïve patients, including patients with a high viral load (> 100,000 copies/ml) and studies in which tenofovir disoproxil was added to stable background therapy (mainly tritherapy) in antiretroviral pre-treated patients experiencing early virological failure (< 10,000 copies/ml, with the majority of patients having < 5,000 copies/ml). Tenofovir disoproxil 245 mg film-coated tablets are also indicated for the treatment of HIV-1 infected adolescents, with NRTI resistance or toxicities precluding the use of first line agents, aged 12 to < 18 years. The choice of tenofovir disoproxil to treat antiretroviral-experienced patients with HIV-1 infection should be based on individual viral resistance testing and/or treatment history of patients. Hepatitis B infection Tenofovir disoproxil 245 mg film-coated tablets are indicated for the treatment of chronic hepatitis B in adults with: compensated liver disease, with evidence of active viral replication, persistently elevated serum alanine aminotransferase (ALT) levels and histological evidence of active inflammation and/or fibrosis. evidence of lamivudine-resistant hepatitis B virus. decompensated liver disease. Tenofovir disoproxil 245 mg film-coated tablets are indicated for the treatment of chronic hepatitis B in adolescents 12 to < 18 years of age with: compensated liver disease and evidence of immune active disease, i.e. active viral replication, persistently elevated serum ALT levels and histological evidence of active inflammation and/or fibrosis.
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。
2026-06-26 · 欧委会决定
2016-12-08 · 获批上市许可
2016-10-13 · CHMP 意见通过
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
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Tenofovir disoproxil Mylan : EPAR - Procedural steps taken and scientific information after authorisation
procedural-steps-after · 2026-10-14
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Tenofovir disoproxil Mylan : EPAR - Risk management plan
rmp-summary · 2026-10-14
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Tenofovir disoproxil Mylan : EPAR - Procedural steps taken and scientific information after authorisation (archive)
procedural-steps-after · 2024-07-19
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Tenofovir disoproxil Mylan-H-C-PSUSA-00002892-201903 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation
scientific-conclusion · 2020-04-03 · EMA/134602/2020
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Tenofovir disoproxil Mylan : EPAR - Public assessment report
assessment-report · 2016-12-19
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Tenofovir disoproxil Mylan : EPAR - Summary for the public
overview · 2016-12-19
产品信息
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Tenofovir disoproxil Viatris : EPAR - All Authorised presentations
all-authorised-presentations · 2026-07-01
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Tenofovir disoproxil Viatris : EPAR - Product information
product-information · 2026-07-01
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Tenofovir disoproxil Viatris : EPAR - Product information - tracked changes
product-information-tracked-changes · 2025-09-09
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。