Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

roche pharma (schweiz) ag - peginterferonum alfa-2a - 5 ml, fertigpen - peginterferonum alfa-2a 180 µg, natrii chloridum, natrii acetas trihydricus, acidum aceticum glaciale, polysorbatum 80, conserv.: alcohol benzylicus 5 mg, aqua ad iniectabilia q.s. ad solutionem pro 0.5 ml. - chronische hepatitis b, chronische hepatitis c - biotechnologika

Unione Europea - italiano - EMA (European Medicines Agency)

aop orphan pharmaceuticals gmbh - ropeginterferon alfa-2b - policitemia vera - immunostimolanti, - besremi è indicato come monoterapia negli adulti per il trattamento della policitemia vera, senza sintomatico splenomegalia.

Unione Europea - italiano - EMA (European Medicines Agency)

schering-plough europe - interferone alfa-2b - hepatitis c, chronic; hepatitis b, chronic - immunostimolanti, - epatite cronica b: trattamento di pazienti adulti con epatite b cronica associata ad evidenza di epatite b replicazione virale (presenza di hbv-dna e hbeag), elevata alanina aminotransferasi (alt) e istologicamente provata, infiammazione epatica attiva e/o fibrosi. epatite cronica c:pazienti adulti:introna è indicato per il trattamento di pazienti adulti con epatite cronica c che abbiano elevati di transaminasi senza scompenso epatico e positivi per hcv-rna sierico o anti-hcv (vedere la sezione 4. il modo migliore per utilizzare introna in questa indicazione è in combinazione con ribavirina. bambini e adolescenti:introna è inteso per l'uso, in un regime di combinazione con ribavirina, per il trattamento di bambini e adolescenti 3 anni di età e anziani, affetti da epatite cronica c, mai trattati in precedenza, senza scompenso epatico, e che sono positivi per hcv-rna sierico. la decisione di trattare deve essere fatta caso per caso, tenendo conto di qualsiasi evidenza di progressione di malattia come l'infiammazione epatica e fibrosi, così come fattori prognostici di risposta, hcv di genotipo e carica virale. l'atteso beneficio del trattamento deve essere pesato contro la sicurezza osservati pazienti pediatrici negli studi clinici (vedere sezioni 4. 4, 4. 8 e 5.

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

alfa biotech s.r.l. - interferone alfa naturale - interferone alfa naturale

Unione Europea - italiano - EMA (European Medicines Agency)

celltrion healthcare hungary kft. - bevacizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - agenti antineoplastici - vegzelma in combination with fluoropyrimidine based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. vegzelma in combination with paclitaxel is indicated for first line treatment of adult patients with metastatic breast cancer. per ulteriori informazioni sullo stato del recettore del fattore di crescita epidermico umano 2 (her2), fare riferimento alla sezione 5. vegzelma in combination with capecitabine is indicated for first line treatment of adult patients with metastatic breast cancer in whom treatment with other chemotherapy options including taxanes or anthracyclines is not considered appropriate. patients who have received taxane and anthracycline containing regimens in the adjuvant setting within the last 12 months should be excluded from treatment with vegzelma in combination with capecitabine. per ulteriori informazioni sullo stato her2, fare riferimento alla sezione 5. vegzelma, in addition to platinum based chemotherapy, is indicated for first line treatment of adult patients with unresectable advanced, metastatic or recurrent non small cell lung cancer (nsclc) other than predominantly squamous cell histology. vegzelma, in combination with erlotinib, is indicated for first line treatment of adult patients with unresectable advanced, metastatic or recurrent nsclc with epidermal growth factor receptor (egfr) activating mutations (see section 5. vegzelma, in combination with interferon alfa 2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. vegzelma, in combination with carboplatin and paclitaxel is indicated for the front line treatment of adult patients with advanced (international federation of gynecology and obstetrics (figo) stages iii b, iii c and iv) epithelial ovarian, fallopian tube, or primary peritoneal cancer (see section 5. vegzelma, in combination with carboplatin and gemcitabine or in combination with carboplatin and paclitaxel, is indicated for treatment of adult patients with first recurrence of platinum sensitive epithelial ovarian, fallopian tube or primary peritoneal cancer who have not received prior therapy with bevacizumab or other vascular endothelial growth factor (vegf) inhibitors or vegf receptor–targeted agents. vegzelma in combination with paclitaxel, topotecan, or pegylated liposomal doxorubicin is indicated for the treatment of adult patients with platinum resistant recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who received no more than two prior chemotherapy regimens and who have not received prior therapy with bevacizumab or other vegf inhibitors or vegf receptor–targeted agents (see section 5. vegzelma, in combination with paclitaxel and cisplatin or, alternatively, paclitaxel and topotecan in patients who cannot receive platinum therapy, is indicated for the treatment of adult patients with persistent, recurrent, or metastatic carcinoma of the cervix (see section 5.

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

msd merck sharp & dohme ag - interferonum alfa-2b adnr - 2 ml, gebrauchsfertige, hsa-freie injektionslösung - interferonum alfa-2b adnr 18 mio u.i., natrii phosphates, dinatrii edetas, natrii chloridum, polysorbatum 80, conserv.: metacresolum 1.8 mg, aqua ad iniectabilia q.s. ad solutionem pro 1.2 ml. - haarzell-leukämie; chronisch myeloische leukämie; multiples myelom; basaliom; melanom; chronische hepatitis c; chronisch aktive hepatitis b; kaposi-sarkom; condylomata acuminata - biotechnologika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

msd merck sharp & dohme ag - peginterferonum alfa-2b - injektionspräparat - praeparatio cryodesiccata: peginterferonum alfa-2b 50 µg, dinatrii phosphas, natrii dihydrogenophosphas dihydricus, saccharum, polysorbatum 80, pro vitro. solvens: aqua ad iniectabilia, q.s. ad solutionem pro 0.5 ml pro vitro. - chronische hepatitis c - biotechnologika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

msd merck sharp & dohme ag - peginterferonum alfa-2b - injektionspräparat - praeparatio cryodesiccata: peginterferonum alfa-2b 50 µg, dinatrii phosphas, natrii dihydrogenophosphas dihydricus, saccharum, polysorbatum 80. solvens: aqua ad iniectabilia q.s. ad solutionem pro 0.5 ml pro vitro. - chronische hepatitis c - biotechnologika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

msd merck sharp & dohme ag - peginterferonum alfa-2b - injektionspräparat - praeparatio cryodesiccata: peginterferonum alfa-2b 80 µg, dinatrii phosphas, natrii dihydrogenophosphas dihydricus, saccharum, polysorbatum 80. solvens: aqua ad iniectabilia q.s. ad solutionem pro 0.5 ml pro vitro. - chronische hepatitis c - biotechnologika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

msd merck sharp & dohme ag - peginterferonum alfa-2b - injektionspräparat - praeparatio cryodesiccata: peginterferonum alfa-2b 100 µg, dinatrii phosphas, natrii dihydrogenophosphas dihydricus, saccharum, polysorbatum 80. solvens: aqua ad iniectabilia q.s. ad solutionem pro 0.5 ml pro vitro. - chronische hepatitis c - biotechnologika