Vegzelma Европска Унија - Чешки - 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 - antineoplastická činidla - 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. další informace o stavu receptoru lidského epidermálního růstového faktoru 2 (her2) naleznete v části 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. další informace o stavu her2 naleznete v části 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.

ACCUSOL 35 Roztok pro hemofiltraci, hemodialýzu a hemodiafiltraci Чешка - Чешки - SUKL (Státní ústav pro kontrolu léčiv)

accusol 35 roztok pro hemofiltraci, hemodialýzu a hemodiafiltraci

nikkiso belgium, tienen array - 5599 dihydrÁt chloridu vÁpenatÉho; 856 hexahydrÁt chloridu hoŘeČnatÉho; 1322 chlorid sodnÝ; 2178 hydrogenuhliČitan sodnÝ - roztok pro hemofiltraci, hemodialýzu a hemodiafiltraci - hemofiltraČnÍ roztoky

ACCUSOL 35 POTASSIUM 2 MMOL/L 2MMOL/L Roztok pro hemofiltraci, hemodialýzu a hemodiafiltraci Чешка - Чешки - SUKL (Státní ústav pro kontrolu léčiv)

accusol 35 potassium 2 mmol/l 2mmol/l roztok pro hemofiltraci, hemodialýzu a hemodiafiltraci

nikkiso belgium, tienen array - 5599 dihydrÁt chloridu vÁpenatÉho; 856 hexahydrÁt chloridu hoŘeČnatÉho; 1322 chlorid sodnÝ; 1174 chlorid draselnÝ; 4957 monohydrÁt glukosy; 2178 hydrogenuhliČitan sodnÝ - roztok pro hemofiltraci, hemodialýzu a hemodiafiltraci - 2mmol/l - hemofiltraČnÍ roztoky

REMODULIN 1MG/ML Infuzní roztok Чешка - Чешки - SUKL (Státní ústav pro kontrolu léčiv)

remodulin 1mg/ml infuzní roztok

ferrer internacional, s.a., barcelona array - 16789 sodnÁ sŮl treprostinilu - infuzní roztok - 1mg/ml - treprostinil

REMODULIN 10MG/ML Infuzní roztok Чешка - Чешки - SUKL (Státní ústav pro kontrolu léčiv)

remodulin 10mg/ml infuzní roztok

ferrer internacional, s.a., barcelona array - 16789 sodnÁ sŮl treprostinilu - infuzní roztok - 10mg/ml - treprostinil

REMODULIN 2,5MG/ML Infuzní roztok Чешка - Чешки - SUKL (Státní ústav pro kontrolu léčiv)

remodulin 2,5mg/ml infuzní roztok

ferrer internacional, s.a., barcelona array - 16789 sodnÁ sŮl treprostinilu - infuzní roztok - 2,5mg/ml - treprostinil

REMODULIN 5MG/ML Infuzní roztok Чешка - Чешки - SUKL (Státní ústav pro kontrolu léčiv)

remodulin 5mg/ml infuzní roztok

ferrer internacional, s.a., barcelona array - 16789 sodnÁ sŮl treprostinilu - infuzní roztok - 5mg/ml - treprostinil

TREPROSTINIL TILLOMED 1MG/ML Infuzní roztok Чешка - Чешки - SUKL (Státní ústav pro kontrolu léčiv)

treprostinil tillomed 1mg/ml infuzní roztok

tillomed pharma gmbh, schönefeld array - 16773 treprostinil - infuzní roztok - 1mg/ml - treprostinil

TREPROSTINIL TILLOMED 10MG/ML Infuzní roztok Чешка - Чешки - SUKL (Státní ústav pro kontrolu léčiv)

treprostinil tillomed 10mg/ml infuzní roztok

tillomed pharma gmbh, schönefeld array - 16773 treprostinil - infuzní roztok - 10mg/ml - treprostinil

TREPROSTINIL TILLOMED 2,5MG/ML Infuzní roztok Чешка - Чешки - SUKL (Státní ústav pro kontrolu léčiv)

treprostinil tillomed 2,5mg/ml infuzní roztok

tillomed pharma gmbh, schönefeld array - 16773 treprostinil - infuzní roztok - 2,5mg/ml - treprostinil