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.

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

fresenius kabi italia s.r.l. - irinotecan - irinotecan

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

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

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

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

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

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

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

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

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

cps cito pharma services gmbh - capecitabinum - compresse rivestite con film - capecitabinum 150 mg, lactosum 15.6 mg, carmellosum natricum solo tenuti insieme corrisp. sodio 1.12 mg, hypromellosum, cellulosum microcristallinum, magnesio stearas, Überzug: hypromellosum, talco, e 171, e 172 (giallo) e 172 (rosso), per compresso haze. - farmaco - synthetika

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

cps cito pharma services gmbh - capecitabinum - compresse rivestite con film - capecitabinum 500 mg, lactosum 52 mg, carmellosum natricum solo tenuti insieme corrisp. sodio 3,75 mg, hypromellosum, cellulosum microcristallinum, magnesio stearas, Überzug: hypromellosum, talco, e 171, e 172 (giallo) e 172 (rosso), per compresso haze. - farmaco - synthetika

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

sandoz pharmaceuticals ag - capecitabinum - capecitabin sandoz 150 mg filmtabletten - capecitabinum 150 mg, excipiens pro compresso obducto. - farmaco - synthetika

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

sandoz pharmaceuticals ag - capecitabinum - capecitabin sandoz 500 mg filmtabletten - capecitabinum 500 mg, excipiens pro compresso obducto. - farmaco - synthetika