Europska Unija - hrvatski - 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.

Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

b. braun adria d.o.o. za proizvodnju, trgovinu i usluge hondlova 2/9 10000 zagreb -

Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

medical intertrade d.o.o., sveta nedelja - in vitro dijagnostika, reagensi za dijagnostiku proteina

Europska Unija - hrvatski - EMA (European Medicines Agency)

amneal pharma europe ltd - l-dopa, карбидопа - parkinsonova bolest - antiparkinsonski lijekovi - simptomatsko liječenje bolesnika s parkinsonovom bolešću.

Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

pharmamed-mado d.o.o. zatišje 8/g 10000 zagreb -

Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

a&b d.o.o., zagreb - in vitro dijagnostika, gotova stakalca za analizu sjemena

Europska Unija - hrvatski - EMA (European Medicines Agency)

abbvie deutschland gmbh co. kg - ritonavir - hiv infekcije - antivirusni lijekovi za sustavnu uporabu - ritonavir je indiciran u kombinaciji s drugim antiretrovirusnim sredstvima za liječenje pacijenata s hiv-1 (odrasli i djeca od dvije godine i stariji).

Europska Unija - hrvatski - EMA (European Medicines Agency)

vifor fresenius medical care renal pharma france - kalcijevu otopinu - hiperkalijemija - lijekovi za liječenje hiperkalemiju i гиперфосфатемии - veltassa je indicirana za liječenje hiperkalemije kod odraslih osoba.

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

intrade pharm d.o.o - željezo (iii) hidroksid saharoza kompleks - rastvor za injekciju/ infuziju - 100 mg/5 ml - 1 ml rastvora sadrži: 20 mg željeza (u obliku kompleksa željezo (iii) hidroksida sa saharozom)

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

licentis doo sarajevo - atrakurijum бесилат - rastvor za injekciju/ infuziju - 25 mg/2.5 ml - 2,5 ml rastvora za injekciju/infuziju sadrži: 25 mg atrakurijum besilata