Vegzelma Avrupa Birliği - Hırvatça - 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 - antineoplastična sredstva - 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. za daljnje informacije o stanju čovjeka epidermalnog faktora rasta receptora 2 (her2), molimo pogledajte odjeljak 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. dodatne informacije o statusu her2 potražite u odjeljku 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.

Tabrecta Avrupa Birliği - Hırvatça - EMA (European Medicines Agency)

tabrecta

novartis europharm limited  - capmatinib dihydrochloride monohydrate - karcinom, ne-malih stanica pluća - antineoplastična sredstva - tabrecta as monotherapy is indicated for the treatment of adult patients with advanced non small cell lung cancer (nsclc) harbouring alterations leading to mesenchymal epithelial transition factor gene exon 14 (metex14) skipping, who require systemic therapy following prior treatment with immunotherapy and/or platinum based chemotherapy.

Jext 150 mikrograma otopina za injekciju u napunjenoj brizgalici Hırvatistan - Hırvatça - HALMED (Agencija za lijekove i medicinske proizvode)

jext 150 mikrograma otopina za injekciju u napunjenoj brizgalici

alk-abelló a/s, boge allé 6-8, horsholm, danska - adrenalintartarat (epinefrintartarat) - otopina za injekciju u napunjenoj brizgalici - urbroj: 1 ml otopine sadrži 1 mg adrenalina (u obliku adrenalintartarata). pojedinačna doza od 0,15 ml otopine za injekciju sadrži 150 mikrograma adrenalina (u obliku adrenalintartarata).

Jext 300 mikrograma otopina za injekciju u napunjenoj brizgalici Hırvatistan - Hırvatça - HALMED (Agencija za lijekove i medicinske proizvode)

jext 300 mikrograma otopina za injekciju u napunjenoj brizgalici

alk-abelló a/s, boge allé 6-8, horsholm, danska - adrenalintartarat (epinefrintartarat) - otopina za injekciju u napunjenoj brizgalici - urbroj: 1 ml otopine sadrži 1 mg adrenalina (u obliku adrenalintartarata). pojedinačna doza od 0,30 ml otopine za injekciju sadrži 300 mikrograma adrenalina (u obliku adrenalintartarata).

Imjudo Avrupa Birliği - Hırvatça - EMA (European Medicines Agency)

imjudo

astrazeneca ab - tremelimumab - carcinoma, hepatocellular - antineoplastična sredstva - imjudo in combination with durvalumab is indicated for the first line treatment of adults with advanced or unresectable hepatocellular carcinoma (hcc). imjudo in combination with durvalumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic non-small cell lung cancer (nsclc) with no sensitising egfr mutations or alk positive mutations.

Tremelimumab AstraZeneca Avrupa Birliği - Hırvatça - EMA (European Medicines Agency)

tremelimumab astrazeneca

astrazeneca ab - tremelimumab - karcinom, ne-malih stanica pluća - antineoplastična sredstva - tremelimumab astrazeneca in combination with durvalumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic non-small cell lung cancer (nsclc) with no sensitising egfr mutations or alk positive mutations.

Enrylaze Avrupa Birliği - Hırvatça - EMA (European Medicines Agency)

enrylaze

jazz pharmaceuticals ireland limited - crisantaspase - prekursorska stanica limfoblastične leukemije-limfom - antineoplastična sredstva - enrylaze is indicated as a component of a multi-agent chemotherapeutic regimen for the treatment of acute lymphoblastic leukaemia (all) and lymphoblastic lymphoma (lbl) in adult and paediatric patients (1 month and older) who developed hypersensitivity or silent inactivation to e. coli-derived asparaginase.

Kaspofungin Pliva 50 mg prašak za koncentrat za otopinu za infuziju Hırvatistan - Hırvatça - HALMED (Agencija za lijekove i medicinske proizvode)

kaspofungin pliva 50 mg prašak za koncentrat za otopinu za infuziju

pliva hrvatska d.o.o., prilaz baruna filipovića 25, zagreb, hrvatska - kaspofunginacetat - prašak za koncentrat za otopinu za infuziju - 50 mg - urbroj: jedna bočica sadrži 50 mg kaspofungina (u obliku kaspofunginacetata)

Kaspofungin Pliva 70 mg prašak za koncentrat za otopinu za infuziju Hırvatistan - Hırvatça - HALMED (Agencija za lijekove i medicinske proizvode)

kaspofungin pliva 70 mg prašak za koncentrat za otopinu za infuziju

pliva hrvatska d.o.o., prilaz baruna filipovića 25, zagreb, hrvatska - kaspofunginacetat - prašak za koncentrat za otopinu za infuziju - 70 mg - urbroj: jedna bočica sadrži 70 mg kaspofungina (u obliku kaspofunginacetata)

Dasatinib Teva 100 mg filmom obložene tablete Hırvatistan - Hırvatça - HALMED (Agencija za lijekove i medicinske proizvode)

dasatinib teva 100 mg filmom obložene tablete

teva b.v., swensweg 5, haarlem, nizozemska - dasatinib hidrat - filmom obložena tableta - 100 mg - urbroj: jedna filmom obložena tableta sadrži 100 mg dasatiniba (u obliku hidrata)