Alymsys Uni Eropa - Bulgar - EMA (European Medicines Agency)

alymsys

mabxience research sl - бевацизумаб - colorectal neoplasms; breast neoplasms; ovarian neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - Антинеопластични средства - alymsys in combination with fluoropyrimidine based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. alymsys in combination with paclitaxel is indicated for first line treatment of adult patients with metastatic breast cancer. alymsys 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 alymsys in combination with capecitabine. alymsys, 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 other than predominantly squamous cell histology. alymsys, in combination with erlotinib, is indicated for first line treatment of adult patients with unresectable advanced, metastatic or recurrent non squamous non small cell lung cancer with epidermal growth factor receptor (egfr) activating mutations. alymsys in combination with interferon alfa 2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. alymsys, 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. alymsys, 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 vegf inhibitors or vegf receptor targeted agents. alymsys, in combination with 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. alymsys, 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.

Oyavas Uni Eropa - Bulgar - EMA (European Medicines Agency)

oyavas

stada arzneimittel ag - бевацизумаб - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - Антинеопластични средства - oyavas in combination with fluoropyrimidine based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. oyavas in combination with paclitaxel is indicated for first line treatment of adult patients with metastatic breast cancer. За повече информация, както за човешкия рецептор на епидермален фактор за растеж 2 (her2 и) статут, моля, вижте раздел 5. oyavas 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 oyavas in combination with capecitabine. За допълнителна информация относно статуса на her2, моля, вижте раздел 5. oyavas, 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 other than predominantly squamous cell histology. oyavas, in combination with erlotinib, is indicated for first line treatment of adult patients with unresectable advanced, metastatic or recurrent non squamous non small cell lung cancer with epidermal growth factor receptor (egfr) activating mutations (see section 5. oyavas in combination with interferon alfa 2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. oyavas, 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. oyavas, 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 vegf inhibitors or vegf receptor–targeted agents. oyavas, in combination with 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. oyavas, 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.

Abraxane Uni Eropa - Bulgar - EMA (European Medicines Agency)

abraxane

bristol-myers squibb pharma eeig - паклитаксел - breast neoplasms; pancreatic neoplasms; carcinoma, non-small-cell lung - Антинеопластични средства - abraxane монотерапия е показан за лечение на метастатичен рак на млечната жлеза при възрастни пациенти, които не първа линия-линия обработка за metastatic на заболяването и за кого е стандартен, антрациклин-съдържаща терапия не е посочено. abraxane в комбинация с гемцитабин е показан за първа линия на лечение при възрастни пациенти с метастатичен аденокарциномы на панкреаса. abraxane в комбинация с карбоплатином е предназначен за първа линия на лечение немелкоклеточного рак на белите дробове при възрастни пациенти, които не са кандидати за потенциално лечебната хирургия и/или лъчетерапия.

Pazenir Uni Eropa - Bulgar - EMA (European Medicines Agency)

pazenir

ratiopharm gmbh - паклитаксел - Неоплазми на гърдата - Антинеопластични средства - pazenir монотерапия е показан за лечение на метастатичен рак на млечната жлеза при възрастни пациенти, които не първа линия-линия обработка за metastatic на заболяването и за кого е стандартен, антрациклин-съдържаща терапия не е посочено. pazenir в комбинация с карбоплатином е предназначен за първа линия на лечение немелкоклеточного рак на белите дробове при възрастни пациенти, които не са кандидати за потенциално лечебната хирургия и/или лъчетерапия.

Apealea Uni Eropa - Bulgar - EMA (European Medicines Agency)

apealea

inceptua ab - паклитаксел - Овариални неоплазми - antineoplastic agents, taxanes - apealea в комбинация с карбоплатином е показан за лечение на възрастни пациенти с първия рецидив платиночувствительный эпителиального на рак на яйчниците, първичен рак на перитонеума и маточните тръби рак.

Nexavar Uni Eropa - Bulgar - EMA (European Medicines Agency)

nexavar

bayer ag - сорафениб - carcinoma, hepatocellular; carcinoma, renal cell - Антинеопластични средства - Гепатоцеллюлярная carcinomanexavar е показан за лечение на карцином гепатоцеллюлярной. Почечно-клетъчен carcinomanexavar е показан за лечение на пациенти с честата почечно-клетъчен карцином, които не по-рано от интерферон-алфа или интерлевкин-2 терапия или се считат за неподходящи за такава терапия. Диференциала на щитовидната жлеза carcinomanexavar е показан за лечение на пациенти с белег, локално-напреднал или метастазирал, диференцирани (папиллярный/фолликулярный/hürthle клетъчния) рак на щитовидната жлеза, рефрактерным до радиоактивному Йоду.

Lextemy Uni Eropa - Bulgar - EMA (European Medicines Agency)

lextemy

mylan ire healthcare limited - бевацизумаб - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - Антинеопластични средства - treatment of carcinoma of the colon or rectum, breast cancer, non-small cell lung cancer, renal cell cancer, epithelial ovarian, fallopian tube or primary peritoneal cancer, and carcinoma of the cervix.

Carboplatin-Teva 10 mg/ml concentrate for solution for infusion Bulgaria - Bulgar - Изпълнителна агенция по лекарствата

carboplatin-teva 10 mg/ml concentrate for solution for infusion

ТЕВА ФАРМАСЮТИКЪЛС БЪЛГАРИЯ ЕООД, - Карбоплатин - 10 mg/ml concentrate for solution for infusion

Carboplatin Ebewe 10 mg/ml concentrate for solution for infusion Bulgaria - Bulgar - Изпълнителна агенция по лекарствата

carboplatin ebewe 10 mg/ml concentrate for solution for infusion

ebewe pharma ges.m.b.h. nfg.kg - Карбоплатин - 10 mg/ml concentrate for solution for infusion

Jemperli Uni Eropa - Bulgar - EMA (European Medicines Agency)

jemperli

glaxosmithkline (ireland) limited - dostarlimab - endometrial neoplasms - antineoplastic agents and antibody drug conjugates - jemparli is indicated as monotherapy for the treatment of adult patients with mismatch repair deficient (dmmr)/microsatellite instability-high (msi h) recurrent or advanced endometrial cancer (ec) that has progressed on or following prior treatment with a platinum-containing regimen.