Եվրոպական Միություն - խորվաթերեն - EMA (European Medicines Agency)

nova laboratories ireland limited - azathioprine - odbacivanje transplantata - imunosupresivi - jayempi is indicated in combination with other immunosuppressive agents for the prophylaxis of transplant rejection in patients receiving allogenic kidney, liver, heart, lung or pancreas transplants. azathioprine is indicated in immunosuppressive regimens as an adjunct to immunosuppressive agents that form the mainstay of treatment (basis immunosuppression). jayempi is used as an immunosuppressant antimetabolite either alone or, more commonly, in combination with other agents (usually corticosteroids) and/ or procedures which influence the immune response. jayempi is indicated in patients who are intolerant to glucocorticosteroids or if the therapeutic response is inadequate despite treatment with high doses of glucocorticosteroids, in the following diseases:severe active rheumatoid arthritis (chronic polyarthritis) that cannot be kept under control by less toxic agents (disease-modifying anti-rheumatic -medicinal products – dmards)auto-immune hepatitis systemic lupus erythematosusdermatomyositispolyarteritis nodosapemphigus vulgaris and bullous pemphigoidbehçet’s diseaserefractory auto-immune haemolytic anaemia, caused by warm igg antibodieschronic refractory idiopathic thrombocytopenic purpurajayempi is used for the treatment of moderately severe to severe forms of chronic inflammatory bowel disease (ibd) (crohn’s disease or ulcerative colitis) in patients in whom glucocorticosteroid therapy is necessary, but where glucocorticosteroids are not tolerated, or in whom the disease is untreatable with other common means of first choice. it is also indicated in adult patients in relapsing multiple sclerosis, if an immunomodulatory therapy is indicated but beta interferon therapy is not possible, or a stable course has been achieved with previous treatment with azathioprine. 3jayempi is indicated for the treatment of generalised myasthenia gravis. depending on the severity of the disease, jayempi should be given in combination with glucocorticosteroids because of slow onset of action at the beginning of treatment and the glucocorticosteroid dose should be gradually reduced after several months of treatment.

Եվրոպական Միություն - խորվաթերեն - EMA (European Medicines Agency)

amgen technology (ireland) uc - Экулизумаб - hemoglobinuria, paroxysmal - imunosupresivi - bekemv is indicated in adults and children for the treatment of paroxysmal nocturnal haemoglobinuria (pnh). dokaza klinički učinak očituje se u bolesnika s гемолизом s klinički simptom(ova), ukazuje na visoke aktivnosti bolesti, bez obzira na priče transfuziju (vidi odjeljak 5.

Խորվաթիա - խորվաթերեն - HALMED (Agencija za lijekove i medicinske proizvode)

biotest pharma gmbh, landsteinerstr. 5, dreieich, njemačka - imunoglobulin protiv citomegalovirusa, людски - otopina za infuziju - 100 u/ml - urbroj: jedan ml otopine za infuziju sadrži: protein ljudske plazme 50 mg (od toga najmanje 96% imunoglobulin g), sa sadržajem antitijela protiv citomegalovirusa (cmv) od 100 u

Խորվաթիա - խորվաթերեն - HALMED (Agencija za lijekove i medicinske proizvode)

biotest pharma gmbh, landsteinerstr. 5, dreieich, njemačka - imunoglobulin protiv hepatitisa b, ljudski, intravenski - otopina za infuziju - 50 iu/ml - urbroj: 1 ml otopine sadrži 50 mg proteina ljudske plazme, od čega je najmanje 96% imunoglobulina g, koji sadrži 50 iu/ml protutijela protiv površinskog antigena virusa hepatitisa b (hbs)

Բոսնիա և Հերցեգովինա - խորվաթերեն - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

inpharm co. d.o.o. banja luka - daratumumab - koncentrat za rastvor za infuziju - 100 mg/5 ml - 1 bočica od 5 ml koncentrata za rastvor za infuziju sadrži: 100 mg daratumumaba

Բոսնիա և Հերցեգովինա - խորվաթերեն - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

inpharm co. d.o.o. banja luka - daratumumab - koncentrat za rastvor za infuziju - 400 mg/20 ml - 1staklena bočica od 20 ml koncentrata za rastvor za infuziju sadrži: 400 mg daratumumaba

Եվրոպական Միություն - խորվաթերեն - EMA (European Medicines Agency)

instituto grifols s.a. - imunoglobulina osoba normalan - mucocutaneous lymph node syndrome; guillain-barre syndrome; bone marrow transplantation; purpura, thrombocytopenic, idiopathic; immunologic deficiency syndromes - imuni serumi i homologna, - replacement therapy in adults, children and adolescents (0-18 years) in: , primary immunodeficiency syndromes with impaired antibody production;, hypogammaglobulinaemia and recurrent bacterial infections in patients with chronic lymphocytic luekaemia, in whom prophylactic antibiotics have failed;, hypogammaglobulinaemia and recurrent bacterial infections in plateau-phase-multiple-myeloma patients who failed to respond to pneumococcal immunisation;, hypogammaglobulinaemia in patients after allogenic haematopoietic-stem-cell transplantation (hsct);, congenital aids with recurrent bacterial infections. , immunomodulation in adults, children and adolescents (0-18 years) in: , primary immune thrombocytopenia (itp), in patients at high risk of bleeding or prior to surgery to correct the platelet count;, guillain barré syndrome;, kawasaki disease.

Բոսնիա և Հերցեգովինա - խորվաթերեն - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

unifarm d.o.o. lukavac - benzilpenicilinkalijum, benzilpenicilinprokain - prašak i rastvarač za rastvor za injekciju - 200000 i.j./1 bočica+ 600000 i.j./1 bočica - 1 bočica praška za rastvor za injekcijusadrži: 125 mg kalijum penicilina g što je ekvivalentno 200 000 i.j./bočici 600 mg prokain penicilina g što je ekvivalentno 600 000 i.j./bočici

Խորվաթիա - խորվաթերեն - HALMED (Agencija za lijekove i medicinske proizvode)

dr. falk pharma gmbh, leinenweberstraße 5, freiburg, njemačka - budezonid - čepić - urbroj: jedan čepić sadrži 4 mg budezonida

Եվրոպական Միություն - խորվաթերեն - EMA (European Medicines Agency)

merck sharp & dohme b.v.  - hepatitis b, rekombinantni površinski antigen - hepatitis b; immunization - cjepiva - 5 micrograms hbvaxpro is indicated for active immunisation against hepatitis-b-virus infection caused by all known subtypes in individuals from birth through 15 years of age considered at risk of exposure to hepatitis-b virus. određene grupe rizika će biti cijepljeni moraju biti definirani na temelju službenih preporuka. može se očekivati da hepatitis d se također može spriječiti putem cijepljenja s hbvaxpro kao što su hepatitis d (uzrokovana agent delta) ne nalazi u nedostatku virusa hepatitis b infekcije. 10 micrograms hbvaxpro is indicated for active immunisation against hepatitis-b-virus infection caused by all known subtypes in individuals 16 years of age or more considered at risk of exposure to hepatitis-b virus. određene grupe rizika će biti cijepljeni moraju biti definirani na temelju službenih preporuka. može se očekivati da hepatitis d se također može spriječiti putem cijepljenja s hbvaxpro kao što su hepatitis d (uzrokovana agent delta) ne nalazi u nedostatku virusa hepatitis b infekcije. 40 micrograms hbvaxpro is indicated for the active immunisation against hepatitis-b-virus infection caused by all known subtypes in predialysis and dialysis adult patients. može se očekivati da hepatitis d također će spriječiti stvaranje imunizacije s hbvaxpro kao što su hepatitis d (uzrokovana agent delta) ne nalazi u nedostatku virusa hepatitisa b .