Bosna i Hercegovina - hrvatski - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

co.medprom d.o.o. banja luka - ифосфамид - prašak za rastvor za injekciju - 2000 mg/1 viala - 1 bočica sa praškom za rastvor za injekciju sadrži: 2000 mg ifosfamid

Europska Unija - hrvatski - EMA (European Medicines Agency)

nanotherapeutics bohumil, s.r.o. - whole virion influenza vaccine, inactivated containing antigen of strain a/california/07/2009 (h1n1)v - disease outbreaks; influenza, human; immunization - cjepiva - profilaksa influence uzrokovana virusom a (h1n1) v 2009. celvapan mora se koristiti u skladu sa službenim vodstvom.

Europska Unija - hrvatski - EMA (European Medicines Agency)

ology bioservices ireland ltd - virusi influence (cijeli virion, inaktivirani), koji sadrže antigen od: a / vietnam / 1203/2004 (h5n1) - influenza, human; immunization; disease outbreaks - cjepiva protiv gripe - aktivna imunizacija protiv h5n1 podtipa virusa influence a. ovaj prikaz se temelji na imunogenosti podataka od ispitanika u dobi od 6 mjeseci i dalje nakon uvođenja dvije doze cjepiva, kuhani s podtipa h5n1 sojeva . vepacel mora se koristiti u skladu sa službenim vodstvom.

Europska Unija - hrvatski - EMA (European Medicines Agency)

novartis europharm limited - basiliksimab - graft rejection; kidney transplantation - imunosupresivi - simulect je indiciran za profilaksu odbacuje organ u de-novo alogene bubrežne transplantacije u odraslih i pedijatrijskih bolesnika (1-17 godina). on će se koristiti paralelno s микроэмульсии циклоспорина i kortikosteroida na temelju imunosupresija kod pacijenata s ploče reaktivnih antitijela manje od 80%, ili u trostrukom popravak иммуносупрессивной terapije, sadrže ciklosporin микроэмульсии, glukokortikoidi i azatioprin ili mikofenolatom мофетил.

Europska Unija - hrvatski - EMA (European Medicines Agency)

immunocore ireland limited - tebentafusp - uveal neoplasms - antineoplastična sredstva - kimmtrak is indicated as monotherapy for the treatment of human leukocyte antigen (hla)-a*02:01-positive adult patients with unresectable or metastatic uveal melanoma.

Europska Unija - hrvatski - EMA (European Medicines Agency)

yes pharmaceutical development services gmbh - doksorubicin hidroklorid - breast neoplasms; ovarian neoplasms; multiple myeloma; sarcoma, kaposi - antineoplastična sredstva - celdoxome pegylated liposomal is indicated in adults:as monotherapy for patients with metastatic breast cancer, where there is an increased cardiac risk. or treatment of advanced ovarian cancer in women who have failed a first-line platinum-based chemotherapy regimen. in combination with bortezomib for the treatment of progressive multiple myeloma in patients who have received at least one prior therapy and who have already undergone or are unsuitable for bone marrow transplant. for treatment of aids-related kaposi’s sarcoma (ks) in patients with low cd4 counts (< 200 cd4 lymphocytes/mm3) and extensive mucocutaneous or visceral disease. celdoxome pegylated liposomal may be used as first-line systemic chemotherapy, or as second line chemotherapy in aids-ks patients with disease that has progressed with, or in patients intolerant to, prior combination systemic chemotherapy comprising at least two of the following agents: a vinca alkaloid, bleomycin and standard doxorubicin (or other anthracycline).