Epclusa Den Europæiske Union - dansk - EMA (European Medicines Agency)

epclusa

gilead sciences ireland uc - sofosbuvir, velpatasvir - hepatitis c kronisk - antivirale midler til systemisk anvendelse - epclusa is indicated for the treatment of chronic hepatitis c virus (hcv) infection in patients 3 years of age and older (see sections 4. 2, 4. 4 og 5.

Sovaldi Den Europæiske Union - dansk - EMA (European Medicines Agency)

sovaldi

gilead sciences ireland uc - sofosbuvir - hepatitis c kronisk - antivirale midler til systemisk anvendelse - sovaldi is indicated in combination with other medicinal products for the treatment of chronic hepatitis c (chc) in adult and paediatric patients aged 3 years and above (see sections 4. 2, 4. 4 og 5. for at hepatitis c virus (hcv) genotype specifik aktivitet, se afsnit 4. 4 og 5. sovaldi is indicated in combination with other medicinal products for the treatment of chronic hepatitis c (chc) in adults and paediatric patients aged 3 years and above (see sections 4. 2, 4. 4 og 5. for at hepatitis c virus (hcv) genotype specifik aktivitet, se afsnit 4. 4 og 5.

Vosevi Den Europæiske Union - dansk - EMA (European Medicines Agency)

vosevi

gilead sciences ireland uc - sofosbuvir, velpatasvir, voxilaprevi - hepatitis c kronisk - antivirale midler til systemisk anvendelse - vosevi is indicated for the treatment of chronic hepatitis c virus (hcv) infection in patients aged 12 years and older and weighing at least 30 kg. (se afsnit 4. 2, 4. 4 og 5.

Harvoni Den Europæiske Union - dansk - EMA (European Medicines Agency)

harvoni

gilead sciences ireland uc - ledipasvir, sofosbuvir - hepatitis c kronisk - antivirale midler til systemisk anvendelse - harvoni is indicated for the treatment of chronic hepatitis c (chc) in adult and paediatric patients aged 3 years and above (see sections 4. 2, 4. 4 og 5. for at hepatitis c virus (hcv) genotype-specifikke aktivitet, se afsnit 4. 4 og 5.

Odefsey Den Europæiske Union - dansk - EMA (European Medicines Agency)

odefsey

gilead sciences ireland uc - emtricitabine, rilpivirine hydrochlorid, tenofovir alafenamide - hiv infektioner - antivirale midler til systemisk anvendelse - behandling af voksne og unge (alderen 12 år og ældre med kroppen vægt mindst 35 kg) inficeret med human immundefekt virus 1 (hiv 1) uden kendte mutationer i forbindelse med resistens over for ikke nucleoside reverse transkriptase inhibitor (nnrti) klasse, tenofovir eller emtricitabine og med en viral belastning ≤ 100.000 hiv 1 rna kopier/ml.

Zepatier Den Europæiske Union - dansk - EMA (European Medicines Agency)

zepatier

merck sharp & dohme b.v. - elbasvir, grazoprevir - hepatitis c kronisk - direct acting antivirals, antivirals for systemic use, antivirals for treatment of hcv infections - zepatier is indicated for the treatment of chronic hepatitis c (chc) in adult and paediatric patients 12 years of age and older who weigh at least 30 kg (see sections 4. 2, 4. 4 og 5. for at hepatitis c virus (hcv) genotype-specifikke aktivitet, se afsnit 4. 4 og 5.

Maviret Den Europæiske Union - dansk - EMA (European Medicines Agency)

maviret

abbvie deutschland gmbh co. kg - glecaprevir, pibrentasvir - hepatitis c kronisk - antivirale midler til systemisk anvendelse - maviret is indicated for the treatment of chronic hepatitis c virus (hcv) infection in adults and children aged 3 years and older. maviret coated granules is indicated for the treatment of chronic hepatitis c virus (hcv) infection in children 3 years and older.

Juluca Den Europæiske Union - dansk - EMA (European Medicines Agency)

juluca

viiv healthcare b.v. - dolutegravir natrium, rilpivirine hydrochlorid - hiv infektioner - antivirale midler til systemisk anvendelse - juluca er indiceret til behandling af human immundefekt virus type 1 (hiv-1) - infektion hos voksne, der er virologically-undertrykt (hiv-1 rna.

Vocabria Den Europæiske Union - dansk - EMA (European Medicines Agency)

vocabria

viiv healthcare b.v. - cabotegavir sodium, cabotegravir - hiv infektioner - antivirale midler til systemisk anvendelse - vocabria tablets are indicated in combination with rilpivirine tablets for the short-term treatment of human immunodeficiency virus type 1 (hiv-1) infection in adults who are virologically suppressed (hiv-1 rna.

Rekambys Den Europæiske Union - dansk - EMA (European Medicines Agency)

rekambys

janssen-cilag international nv - rilpivirine - hiv infektioner - antivirale midler til systemisk anvendelse - rekambys is indicated, in combination with cabotegravir injection, for the treatment of human immunodeficiency virus type 1 (hiv 1) infection in adults who are virologically suppressed (hiv-1 rna < 50 copies/ml) on a stable antiretroviral regimen without present or past evidence of viral resistance to, and no prior virological failure with, agents of the nnrti and ini class.