Xevudy Evropská unie - čeština - EMA (European Medicines Agency)

xevudy

glaxosmithkline trading services limited - sotrovimab - covid-19 virus infection - imunitní séra a imunoglobuliny, - xevudy is indicated for the treatment of adults and adolescents (aged 12 years and over and weighing at least 40 kg) with coronavirus disease 2019 (covid-19) who do not require oxygen supplementation and who are at increased risk of progressing to severe covid-19.

Vegzelma Evropská unie - čeština - 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.

Spevigo Evropská unie - čeština - EMA (European Medicines Agency)

spevigo

boehringer ingelheim international gmbh - spesolimab - psoriáza - imunosupresiva - spevigo is indicated for the treatment of flares in adult patients with generalised pustular psoriasis (gpp) as monotherapy.

AMESOS 10MG/5MG Tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

amesos 10mg/5mg tableta

gedeon richter plc., budapešť array - 12970 dihydrÁt lisinoprilu; 12990 amlodipin-besilÁt - tableta - 10mg/5mg - lisinopril a amlodipin

AMESOS 20MG/10MG Tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

amesos 20mg/10mg tableta

gedeon richter plc., budapešť array - 12970 dihydrÁt lisinoprilu; 12990 amlodipin-besilÁt - tableta - 20mg/10mg - lisinopril a amlodipin

AMESOS 20MG/5MG Tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

amesos 20mg/5mg tableta

gedeon richter plc., budapešť array - 12970 dihydrÁt lisinoprilu; 12990 amlodipin-besilÁt - tableta - 20mg/5mg - lisinopril a amlodipin

CAZAPROL 0,5MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

cazaprol 0,5mg potahovaná tableta

krka, d.d., novo mesto, novo mesto array - 12895 monohydrÁt cilazaprilu - potahovaná tableta - 0,5mg - cilazapril

CAZAPROL 1MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

cazaprol 1mg potahovaná tableta

krka, d.d., novo mesto, novo mesto array - 12895 monohydrÁt cilazaprilu - potahovaná tableta - 1mg - cilazapril

CAZAPROL 2,5MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

cazaprol 2,5mg potahovaná tableta

krka, d.d., novo mesto, novo mesto array - 12895 monohydrÁt cilazaprilu - potahovaná tableta - 2,5mg - cilazapril

CAZAPROL 5MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

cazaprol 5mg potahovaná tableta

krka, d.d., novo mesto, novo mesto array - 12895 monohydrÁt cilazaprilu - potahovaná tableta - 5mg - cilazapril