Gembin 40 mg/ml koncentrāts infūziju šķīduma pagatavošanai Latvia - latvisk - Zāļu valsts aģentūra

gembin 40 mg/ml koncentrāts infūziju šķīduma pagatavošanai

actavis group ptc ehf., iceland - gemcitabīns - koncentrāts infūziju šķīduma pagatavošanai - 40 mg/ml

Gemcitabine Hydrochloride Accord 1 g pulveris infūziju šķīduma pagatavošanai Latvia - latvisk - Zāļu valsts aģentūra

gemcitabine hydrochloride accord 1 g pulveris infūziju šķīduma pagatavošanai

accord healthcare b.v., netherlands - gemcitabīns - pulveris infūziju šķīduma pagatavošanai - 1 g

Gemcitabine Hydrochloride Accord 2 g pulveris infūziju šķīduma pagatavošanai Latvia - latvisk - Zāļu valsts aģentūra

gemcitabine hydrochloride accord 2 g pulveris infūziju šķīduma pagatavošanai

accord healthcare b.v., netherlands - gemcitabīns - pulveris infūziju šķīduma pagatavošanai - 2 g

Gemcitabine Hydrochloride Accord 200 mg pulveris infūziju šķīduma pagatavošanai Latvia - latvisk - Zāļu valsts aģentūra

gemcitabine hydrochloride accord 200 mg pulveris infūziju šķīduma pagatavošanai

accord healthcare b.v., netherlands - gemcitabīns - pulveris infūziju šķīduma pagatavošanai - 200 mg

Gemcitabine medac 38 mg/ml koncentrāts infūziju šķīduma pagatavošanai Latvia - latvisk - Zāļu valsts aģentūra

gemcitabine medac 38 mg/ml koncentrāts infūziju šķīduma pagatavošanai

medac gesellschaft für klinische spezialpräparate mbh, germany - gemcitabīns - koncentrāts infūziju šķīduma pagatavošanai - 38 mg/ml

Gemcitabine Accord 100 mg/ml koncentrāts infūziju šķīduma pagatavošanai Latvia - latvisk - Zāļu valsts aģentūra

gemcitabine accord 100 mg/ml koncentrāts infūziju šķīduma pagatavošanai

accord healthcare b.v., netherlands - gemcitabīns - koncentrāts infūziju šķīduma pagatavošanai - 100 mg/ml

Gemcit 38 mg/ml pulveris infūziju šķīduma pagatavošanai Latvia - latvisk - Zāļu valsts aģentūra

gemcit 38 mg/ml pulveris infūziju šķīduma pagatavošanai

fresenius kabi polska sp.z o.o., poland - gemcitabīns - pulveris infūziju šķīduma pagatavošanai - 38 mg/ml

Gemcitabine Kabi 38 mg/ml koncentrāts infūziju šķīduma pagatavošanai Latvia - latvisk - Zāļu valsts aģentūra

gemcitabine kabi 38 mg/ml koncentrāts infūziju šķīduma pagatavošanai

fresenius kabi polska sp.z o.o., poland - gemcitabīns - koncentrāts infūziju šķīduma pagatavošanai - 38 mg/ml

Gemsol 40 mg/ml koncentrāts infūziju šķīduma pagatavošanai Latvia - latvisk - Zāļu valsts aģentūra

gemsol 40 mg/ml koncentrāts infūziju šķīduma pagatavošanai

sandoz d.d., slovenia - gemcitabīns - koncentrāts infūziju šķīduma pagatavošanai - 40 mg/ml

Vegzelma Den europeiske union - italiensk - EMA (European Medicines Agency)

vegzelma

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.