Pegasys-Met 135mcg/0,5 ml Soluzione iniettabile in siringa Preriempita Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

pegasys-met 135mcg/0,5 ml soluzione iniettabile in siringa preriempita

roche pharma (schweiz) ag - peginterferonum alfa-2a - soluzione iniettabile in siringa preriempita - peginterferonum alfa-2a 135 µg, natrii chloridum, natrii acetas trihydricus, acidum aceticum glaciale, dl-methioninum, polysorbatum 20, natrii acetas trihydricus aut acidum aceticum ad ph, aqua ad iniectabile q.s. ad solutionem pro 0.5 ml corresp. natrium 1.8 mg. - chronische epatite b; chronische epatite c - biotechnologika

Pegasys-Met 180mcg/0,5 ml Soluzione iniettabile in siringa Preriempita Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

pegasys-met 180mcg/0,5 ml soluzione iniettabile in siringa preriempita

roche pharma (schweiz) ag - peginterferonum alfa-2a - soluzione iniettabile in siringa preriempita - peginterferonum alfa-2a 180 µg, natrii chloridum, natrii acetas trihydricus, acidum aceticum glaciale, polysorbatum 20, natrii acetas trihydricus aut acidum aceticum ad ph, dl-methioninum, aqua ad iniectabile q.s. ad solutionem pro 0.5 ml corresp. natrium 1.8 mg. - chronische epatite b; chronische epatite c - biotechnologika

ROFERON A Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

roferon a

roche s.p.a. - interferone alfa-2a - interferone alfa-2a

Roferon-A 3 Mio I.E./0,5 mL Soluzione iniettabile in siringa Preriempita Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

roferon-a 3 mio i.e./0,5 ml soluzione iniettabile in siringa preriempita

roche pharma (schweiz) ag - interferonum alfa-2a adnr - soluzione iniettabile in siringa preriempita - interferonum alfa-2a adnr 3 milioni di u. i., natrii chloridum, ammonii acetas, alcol benzylicus 5 mg, polysorbatum 80, acido aceticum glaciale o natrii hydroxidum, acqua ad iniectabilia q.s. per una soluzione invece di 0,5 ml corrisp. sodio 1.42 mg. - leucemia a cellule capellute; kutanes cellule t linfoma; cml; sarcoma di kaposi; melanoma; carcinoma a cellule renali; cronica epatite c; epatite cronica b - biotechnologika

Roferon-A 4,5 Mio I.E./0,5 mL Soluzione iniettabile in siringa Preriempita Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

roferon-a 4,5 mio i.e./0,5 ml soluzione iniettabile in siringa preriempita

roche pharma (schweiz) ag - interferonum alfa-2a adnr - soluzione iniettabile in siringa preriempita - interferonum alfa-2a adnr 4,5 mio u. i., natrii chloridum, ammonii acetas, alcol benzylicus 5 mg, polysorbatum 80, acido aceticum glaciale o natrii hydroxidum, acqua ad iniectabilia q.s. per una soluzione invece di 0,5 ml corrisp. sodio 1.42 mg. - leucemia a cellule capellute; kutanes cellule t linfoma; cml; sarcoma di kaposi; melanoma; carcinoma a cellule renali; cronica epatite c; epatite cronica b - biotechnologika

Roferon-A 6 Mio I.E./0,5 mL Soluzione iniettabile in siringa Preriempita Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

roferon-a 6 mio i.e./0,5 ml soluzione iniettabile in siringa preriempita

roche pharma (schweiz) ag - interferonum alfa-2a adnr - soluzione iniettabile in siringa preriempita - interferonum alfa-2a adnr 6 milioni di u. i., natrii chloridum, ammonii acetas, alcol benzylicus 5 mg, polysorbatum 80, acido aceticum glaciale o natrii hydroxidum, acqua ad iniectabilia q.s. per una soluzione invece di 0,5 ml di sodio 1.42 mg. - leucemia a cellule capellute; kutanes cellule t linfoma; cml; sarcoma di kaposi; melanoma; carcinoma a cellule renali; cronica epatite c; epatite cronica b - biotechnologika

Roferon-A 9 Mio I.E./0,5 mL Soluzione iniettabile in siringa Preriempita Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

roferon-a 9 mio i.e./0,5 ml soluzione iniettabile in siringa preriempita

roche pharma (schweiz) ag - interferonum alfa-2a adnr - soluzione iniettabile in siringa preriempita - interferonum alfa-2a adnr 9 mio di u. i., natrii chloridum, ammonii acetas, alcol benzylicus 5 mg, polysorbatum 80, acido aceticum glaciale o natrii hydroxidum, acqua ad iniectabilia q.s. per una soluzione invece di 0,5 ml di sodio 1.42 mg. - leucemia a cellule capellute; kutanes cellule t linfoma; cml; sarcoma di kaposi; melanoma; carcinoma a cellule renali; cronica epatite c; epatite cronica b - biotechnologika

Zepatier Unione Europea - italiano - EMA (European Medicines Agency)

zepatier

merck sharp & dohme b.v. - elbasvir, grazoprevir - epatite c, cronica - 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 e 5. per il virus dell'epatite c (hcv) di genotipo-specifici di attività, vedere sezioni 4. 4 e 5.

Maviret Unione Europea - italiano - EMA (European Medicines Agency)

maviret

abbvie deutschland gmbh co. kg - glecaprevir, pibrentasvir - epatite c, cronica - antivirali per uso sistemico - 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.

Jayempi Unione Europea - italiano - EMA (European Medicines Agency)

jayempi

nova laboratories ireland limited - azathioprine - reiezione del trapianto - immunosoppressori - jayempi is indicated in combination with other immunosuppressive agents for the prophylaxis of transplant rejection in patients receiving allogenic kidney, liver, heart, lung or pancreas transplants. azathioprine is indicated in immunosuppressive regimens as an adjunct to immunosuppressive agents that form the mainstay of treatment (basis immunosuppression). jayempi is used as an immunosuppressant antimetabolite either alone or, more commonly, in combination with other agents (usually corticosteroids) and/ or procedures which influence the immune response. jayempi is indicated in patients who are intolerant to glucocorticosteroids or if the therapeutic response is inadequate despite treatment with high doses of glucocorticosteroids, in the following diseases:severe active rheumatoid arthritis (chronic polyarthritis) that cannot be kept under control by less toxic agents (disease-modifying anti-rheumatic -medicinal products – dmards)auto-immune hepatitis systemic lupus erythematosusdermatomyositispolyarteritis nodosapemphigus vulgaris and bullous pemphigoidbehçet’s diseaserefractory auto-immune haemolytic anaemia, caused by warm igg antibodieschronic refractory idiopathic thrombocytopenic purpurajayempi is used for the treatment of moderately severe to severe forms of chronic inflammatory bowel disease (ibd) (crohn’s disease or ulcerative colitis) in patients in whom glucocorticosteroid therapy is necessary, but where glucocorticosteroids are not tolerated, or in whom the disease is untreatable with other common means of first choice. it is also indicated in adult patients in relapsing multiple sclerosis, if an immunomodulatory therapy is indicated but beta interferon therapy is not possible, or a stable course has been achieved with previous treatment with azathioprine. 3jayempi is indicated for the treatment of generalised myasthenia gravis. depending on the severity of the disease, jayempi should be given in combination with glucocorticosteroids because of slow onset of action at the beginning of treatment and the glucocorticosteroid dose should be gradually reduced after several months of treatment.