COLECALCIFEROL RADAYDRUG 30000 RÜ õhukese polümeerikattega tablett Eesti - eesti - Ravimiamet

colecalciferol radaydrug 30000 rü õhukese polümeerikattega tablett

radaydrug kft. - kolekaltsiferool - õhukese polümeerikattega tablett - 30000rÜ 1tk; 30000rÜ 3tk; 30000rÜ 2tk

COLECALCIFEROL RADAYDRUG 7000 RÜ õhukese polümeerikattega tablett Eesti - eesti - Ravimiamet

colecalciferol radaydrug 7000 rü õhukese polümeerikattega tablett

radaydrug kft. - kolekaltsiferool - õhukese polümeerikattega tablett - 7000rÜ 4tk; 7000rÜ 8tk; 7000rÜ 12tk

SORAFENIB TEVA õhukese polümeerikattega tablett Eesti - eesti - Ravimiamet

sorafenib teva õhukese polümeerikattega tablett

teva b.v. - sorafeniib - õhukese polümeerikattega tablett - 200mg 112tk

COLECALCIFEROL RADAYDRUG 1000 RÜ õhukese polümeerikattega tablett Eesti - eesti - Ravimiamet

colecalciferol radaydrug 1000 rü õhukese polümeerikattega tablett

radaydrug kft. - kolekaltsiferool - õhukese polümeerikattega tablett - 1000rÜ 30tk; 1000rÜ 90tk; 1000rÜ 60tk

COLECALCIFEROL RADAYDRUG 800 RÜ õhukese polümeerikattega tablett Eesti - eesti - Ravimiamet

colecalciferol radaydrug 800 rü õhukese polümeerikattega tablett

radaydrug kft. - kolekaltsiferool - õhukese polümeerikattega tablett - 800rÜ 30tk; 800rÜ 60tk; 800rÜ 90tk

SORAFENIB ZENTIVA õhukese polümeerikattega tablett Eesti - eesti - Ravimiamet

sorafenib zentiva õhukese polümeerikattega tablett

zentiva k.s. - sorafeniib - õhukese polümeerikattega tablett - 200mg 112tk

Voxzogo Euroopa Liit - eesti - EMA (European Medicines Agency)

voxzogo

biomarin international limited - vosoritide - achondroplasia - narkootikumid luuhaiguste raviks - voxzogo is indicated for the treatment of achondroplasia in patients 4 months of age and older whose epiphyses are not closed. the diagnosis of achondroplasia should be confirmed by appropriate genetic testing.

XORAFIA õhukese polümeerikattega tablett Eesti - eesti - Ravimiamet

xorafia õhukese polümeerikattega tablett

lv system service sia - sorafeniib - õhukese polümeerikattega tablett - 200mg 112tk

Vegzelma Euroopa Liit - eesti - EMA (European Medicines Agency)

vegzelma

celltrion healthcare hungary kft. - bevatsizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - antineoplastilised ained - 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. lisateavet inimese epidermaalse kasvufaktori retseptori 2 (her2) seisundi kohta vt palun 5. jaotisest. 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. her2 staatuse kohta lisateabe saamiseks lugege palun 5. jaotist. 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.

Hyftor Euroopa Liit - eesti - EMA (European Medicines Agency)

hyftor

plusultra pharma gmbh - sirolimus - angiofibroma; tuberous sclerosis - hyftor is indicated for the treatment of facial angiofibroma associated with tuberous sclerosis complex in adults and paediatric patients aged 6 years and older.