Bosnie-Herzégovine - croate - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

roche d.o.o.roche ltd. - atezolizumab - koncentrat za otopinu za infuziju - 60 mg/1 ml - 1 ml koncentrata za otopinu za infuziju sadrži: 60 mg atezolizumaba (20 ml koncentrata za otopinu za infuziju sadrži 1200 mg atezolizumaba)

Bosnie-Herzégovine - croate - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

roche d.o.o.roche ltd. - atezolizumab - koncentrat za otopinu za infuziju - 60 mg/1 ml - 14 ml koncentrata za otopinu za infuziju sadrži: 840 mg atezolizumaba (60 mg/ml)

Union européenne - croate - EMA (European Medicines Agency)

roche registration gmbh - atezolizumab - carcinoma, transitional cell; carcinoma, non-small-cell lung; urologic neoplasms; breast neoplasms; small cell lung carcinoma - antineoplastična sredstva - urothelial carcinomatecentriq as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic urothelial carcinoma (uc):- after prior platinum containing chemotherapy, or - who are considered cisplatin ineligible, and whose tumours have a pd-l1 expression ≥ 5% (see section 5. non-small cell lung cancer tecentriq, in combination with bevacizumab, paclitaxel and carboplatin, is indicated for the first-line treatment of adult patients with metastatic non-squamous non small cell lung cancer (nsclc). in patients with egfr mutant or alk-positive nsclc, tecentriq, in combination with bevacizumab, paclitaxel and carboplatin, is indicated only after failure of appropriate targeted therapies (see section 5. tecentriq, in combination with nab paclitaxel and carboplatin, is indicated for the first line treatment of adult patients with metastatic non-squamous nsclc who do not have egfr mutant or alk positive nsclc (see section 5. tecentriq as monotherapy is indicated for the first-line treatment of adult patients with metastatic non-small cell lung cancer (nsclc) whose tumours have a pd-l1 expression ≥ 50% tumour cells (tc) or ≥ 10% tumour-infiltrating immune cells (ic) and who do not have egfr mutant or alk-positive nsclc (see section 5. tecentriq u monoterapiji namijenjen za liječenje odraslih bolesnika s lokalno-uobičajena ili metastatskih НМРЛ nakon što je ranije kemoterapije. patients with egfr mutant or alk positive nsclc should also have received targeted therapies before receiving tecentriq (see section 5. small cell lung cancertecentriq, in combination with carboplatin and etoposide, is indicated for the first-line treatment of adult patients with extensive-stage small cell lung cancer (es-sclc) (see section 5. hepatocellular carcinomatecentriq, in combination with bevacizumab, is indicated for the treatment of adult patients with advanced or unresectable hepatocellular carcinoma (hcc) who have not received prior systemic therapy (see section 5. urothelial carcinomatecentriq as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic urothelial carcinoma (uc):- after prior platinum containing chemotherapy, or- who are considered cisplatin ineligible, and whose tumours have a pd-l1 expression ≥ 5% (see section 5. non-small cell lung cancertecentriq as monotherapy is indicated for the first-line treatment of adult patients with metastatic non-small cell lung cancer (nsclc) whose tumours have a pd-l1 expression ≥ 50% tumour cells (tc) or ≥ 10% tumour-infiltrating immune cells (ic) and who do not have egfr mutant or alk-positive nsclc (see section 5. tecentriq u monoterapiji namijenjen za liječenje odraslih bolesnika s lokalno-uobičajena ili metastatskih НМРЛ nakon što je ranije kemoterapije. patients with egfr mutant or alk positive nsclc should also have received targeted therapies before receiving tecentriq (see section 5. triple-negative breast cancertecentriq in combination with nab-paclitaxel is indicated for the treatment of adult patients with unresectable locally advanced or metastatic triple-negative breast cancer (tnbc) whose tumours have pd-l1 expression ≥ 1% and who have not received prior chemotherapy for metastatic disease.

Monténégro - croate - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

"hoffmann-la roche ltd" d.s.d. podgorica - atezolizumab - koncentrat za rastvor za infuziju - 840mg/14ml

Monténégro - croate - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

"hoffmann-la roche ltd" d.s.d. podgorica - atezolizumab - koncentrat za rastvor za infuziju - 1200mg/20ml

Union européenne - croate - EMA (European Medicines Agency)

glaxosmithkline trading services - mepolizumab - astma - lijekovi za opstruktivne plućne bolesti dišnih putova, - severe eosinophilic asthmanucala is indicated as an add-on treatment for severe refractory eosinophilic asthma in adults, adolescents and children aged 6 years and older. chronic rhinosinusitis with nasal polyps (crswnp)nucala is indicated as an add-on therapy with intranasal corticosteroids for the treatment of adult patients with severe crswnp for whom therapy with systemic corticosteroids and/or surgery do not provide adequate control. eosinophilic granulomatosis with polyangiitis (egpa)nucala is indicated as an add-on treatment for patients aged 6 years and older with relapsing-remitting or refractory eosinophilic granulomatosis with polyangiitis (egpa). hypereosinophilic syndrome (hes)nucala is indicated as an add-on treatment for adult patients with inadequately controlled hypereosinophilic syndrome without an identifiable non-haematologic secondary cause.

Bosnie-Herzégovine - croate - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

takeda pharmaceuticals bh d.o.o. sarajevo - vedolizumab - rastvor za injekciju u napunjenoj šprici - 108 mg/1 šprica - 1 napunjena šprica sa 0,68 ml rastvora za injekciju sadrži: 108 mg vedolizumaba

Union européenne - croate - EMA (European Medicines Agency)

takeda pharma a/s - vedolizumab - colitis, ulcerative; crohn disease - selektivni imunosupresivi - colitisentyvio ulcerozni indiciran za liječenje odraslih bolesnika s вмеру na strogo aktivno язвенному колиту, koji su imali neadekvatan odgovor, izgubila odgovor, ili iz netrpeljivosti ili tradicionalne terapije ili faktor nekroze tumora alfa (Фноа) antagonist. diseaseentyvio kruna je indiciran za liječenje odraslih bolesnika s bolešću reumatoidnim kruna, koji su imali neadekvatan odgovor, izgubila odgovor, ili iz netrpeljivosti ili tradicionalne terapije ili faktor nekroze tumora alfa (Фноа) antagonist. pouchitisentyvio is indicated for the treatment of adult patients with moderately to severely active chronic pouchitis, who have undergone proctocolectomy and ileal pouch anal anastomosis for ulcerative colitis, and have had an inadequate response with or lost response to antibiotic therapy.

Bosnie-Herzégovine - croate - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

takeda pharmaceuticals bh d.o.o. sarajevo - vedolizumab - prašak za koncentrat za otopinu za infuziju - 300 mg/1 bočica - 1 bočica praška za koncentrat za otopinu za infuziju sadrži: 300 mg vedolizumab

Monténégro - croate - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

druŠtvo za trgovinu na veliko farmaceutskim proizvodima "glosarij" d.o.o.-podgorica - vedolizumab - rastvor za injekciju u napunjenom injekcionom penu - 108mg/0.68ml