רומניה - רומנית - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

gilead sciences ireland uc - irlanda - sofosbuvirum +velpatasvirum + voxilaprevirum - compr. film. - 400mg/100mg/100mg - antivirale cu actiune directa

האיחוד האירופי - רומנית - EMA (European Medicines Agency)

gilead sciences ireland uc - emtricitabină, tenofovir alafenamide - infecții cu hiv - antivirale pentru uz sistemic - descovy is indicated in combination with other antiretroviral agents for the treatment of adults and adolescents (aged 12 years and older with body weight at least 35 kg) infected with human immunodeficiency virus type 1 (hiv-1).

האיחוד האירופי - רומנית - EMA (European Medicines Agency)

gilead sciences ireland uc - sofosbuvir, velpatasvir - hepatita c, cronică - antivirale pentru uz sistemic - 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 și 5.

האיחוד האירופי - רומנית - EMA (European Medicines Agency)

gilead sciences ireland uc - ledipasvir, sofosbuvir - hepatita c, cronică - antivirale pentru uz sistemic - 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 și 5. pentru virusul hepatitei c (vhc) genotip-activitatea specifică a se vedea secțiunile 4. 4 și 5.

האיחוד האירופי - רומנית - EMA (European Medicines Agency)

gilead sciences ireland uc - idelalisibul - lymphoma, non-hodgkin; leukemia, lymphocytic, chronic, b-cell - antineoplastic agents, other antineoplastic agents - zydelig is indicated in combination with an anti‑cd20 monoclonal antibody (rituximab or ofatumumab) for the treatment of adult patients with chronic lymphocytic leukaemia (cll):who have received at least one prior therapy, oras first line treatment in the presence of 17p deletion or tp53 mutation in patients who are not eligible for any other therapies. zydelig is indicated as monotherapy for the treatment of adult patients with follicular lymphoma (fl) that is refractory to two prior lines of treatment.

האיחוד האירופי - רומנית - EMA (European Medicines Agency)

gilead sciences ireland uc - cobicistat - infecții cu hiv - antivirale pentru uz sistemic - tybost is indicated as a pharmacokinetic enhancer of atazanavir 300 mg once daily or darunavir 800 mg once daily as part of antiretroviral combination therapy in human immunodeficiency virus-1 (hiv-1) infected adults and adolescents aged 12 years and older:weighing at least 35 kg co‑administered with atazanavir orweighing at least 40 kg co‑administered with darunavir.

האיחוד האירופי - רומנית - EMA (European Medicines Agency)

gilead sciences ireland uc - tenofovir alafenamid fumarat - hepatita b - antivirale pentru uz sistemic - vemlidy is indicated for the treatment of chronic hepatitis b (chb) in adults and paediatric patients 6 years of age and older weighing at least 25 kg (see section 5.

האיחוד האירופי - רומנית - EMA (European Medicines Agency)

gilead sciences ireland uc - sofosbuvir - hepatita c, cronică - antivirale pentru uz sistemic - 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 și 5. pentru virusul hepatitei c (vhc) genotip specific de activitate, a se vedea secțiunile 4. 4 și 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 și 5. pentru virusul hepatitei c (vhc) genotip specific de activitate, a se vedea secțiunile 4. 4 și 5.

האיחוד האירופי - רומנית - EMA (European Medicines Agency)

gilead sciences ireland uc - sofosbuvir, velpatasvir, voxilaprevi - hepatita c, cronică - antivirale pentru uz sistemic - 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. (a se vedea secțiunile 4. 2, 4. 4 și 5.

האיחוד האירופי - רומנית - EMA (European Medicines Agency)

gilead sciences ireland uc - bictegravir, emtricitabină, tenofovir alafenamide, fumarat - infecții cu hiv - antivirale pentru uz sistemic - biktarvy is indicated for the treatment of human immunodeficiency virus 1 (hiv 1) infection in adults and paediatric patients at least 2 years of age and weighing at least 14 kg i without present or past evidence of viral resistance to the integrase inhibitor class, emtricitabine or tenofovir. (vezi secțiunea 5.