法规知识库 · EMA 集中审评
Darunavir Krka d.d.
darunavir · EMEA/H/C/004891 · 已过期
获批上市许可
2018-01-18
欧委会决定日
2023-01-22
持有人 / 申请人
KRKA tovarna zdravil d.d. Novo mesto
终止日期字段
2023-01-22
从产品到官方文件
文件记录
5
官方索引 5
EPAR / 审评
3
assessment / overview 等
产品信息
2
PI / presentations
其他
0
RMP / PIP 等
ATC:J05AE10
治疗领域:HIV Infections
药理分类:Antivirals for systemic use
修订号:8 · 最新影响 PI 的程序:IB/0011
适应症(原文):400mg and 800 mg Film-coated Tablets Darunavir Krka d.d., co-administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (HIV-1) infection. Darunavir Krka d.d., co-administered with cobicistat is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (HIV-1) infection in adult patients (see section 4.2). Darunavir Krka d.d. 400 mg and 800 mg tablets may be used to provide suitable dose regimens for the treatment of HIV-1 infection in adult and paediatric patients from the age of 3 years and at least 40 kg body weight who are: antiretroviral therapy (ART)-naïve (see section 4.2). ART-experienced with no darunavir resistance associated mutations (DRV-RAMs) and who have plasma HIV-1 RNA < 100,000 copies/ml and CD4+ cell count ? 100 cells x 106/l. In deciding to initiate treatment with darunavir in such ART-experienced patients, genotypic testing should guide the use of darunavir (see sections 4.2, 4.3, 4.4 and 5.1). 600mg Film-coated Tablets Darunavir Krka d.d., co-administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (HIV-1) infection. Darunavir Krka d.d. 600 mg tablets may be used to provide suitable dose regimens (see section 4.2): For the treatment of HIV-1 infection in antiretroviral treatment (ART)-experienced adult patients, including those that have been highly pre-treated. For the treatment of HIV-1 infection in paediatric patients from the age of 3 years and at least 15 kg body weight. In deciding to initiate treatment with darunavir co-administered with low dose ritonavir, careful consideration should be given to the treatment history of the individual patient and the patterns of mutations associated with different agents. Genotypic or phenotypic testing (when available) and treatment history should guide the use of darunavir.
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。
2023-01-22 · 欧委会决定
2023-01-22 · 上市许可终止(撤市/失效/撤销等)
Expired
2018-01-18 · 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 ↗
Darunavir Krka d.d. : EPAR - Procedural steps taken and scientific information after authorisation
procedural-steps-after · 2023-02-03
- 打开官方文件 ↗
Darunavir Krka d.d. : EPAR - Summary for the public
overview · 2023-02-03
- 打开官方文件 ↗
Darunavir Krka d.d. : EPAR - Public assessment report
assessment-report · 2023-02-03 · EMA/786962/2017
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。