Evropska unija - slovenščina - EMA (European Medicines Agency)

instituto grifols s.a. - Človekove normalno imunoglobulina - mucocutaneous lymph node syndrome; guillain-barre syndrome; bone marrow transplantation; purpura, thrombocytopenic, idiopathic; immunologic deficiency syndromes - imunski sera in imunoglobulini, - 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.

Evropska unija - slovenščina - EMA (European Medicines Agency)

glaxo group ltd. - amprenavir - okužbe z virusom hiv - antivirusi za sistemsko uporabo - zdravilo agenerase, v kombinaciji z drugimi protiretrovirusnimi zdravili, je indicirano za zdravljenje zaviralcev proteaze (pi), ki so se doživeli odrasli in otroci, okuženi s hiv-1, in njihovi otroci, starejši od 4 let. kapsule agenerase je običajno treba dajati z majhnim odmerkom ritonavirja kot farmakokinetičnega povečevalnika amprenavirja (glejte poglavja 4. 2 in 4. izbira amprenavirja mora temeljiti na testiranju odpornosti na posamezne virusne odmerke in zgodovini zdravljenja bolnikov (glejte poglavje 5). koristi agenerase razširila z ritonavir ni bila dokazana v pi ladjo bolnikih (glejte poglavje 5.

Evropska unija - slovenščina - EMA (European Medicines Agency)

kyowa kirin holdings b.v. - burosumab - hypophosphatemia, familial; hypophosphatemic rickets, x-linked dominant; osteomalacia - zdravila za zdravljenje bolezni kosti - crysvita is indicated for the treatment of x-linked hypophosphataemia, in children and adolescents aged 1 to 17 years with radiographic evidence of bone disease, and in adults. crysvita is indicated for the treatment of fgf23-related hypophosphataemia in tumour-induced osteomalacia associated with phosphaturic mesenchymal tumours that cannot be curatively resected or localised in children and adolescents aged 1 to 17 years and in adults.

Evropska unija - slovenščina - EMA (European Medicines Agency)

vifor fresenius medical care renal pharma france - prostate sorbiteksa kalcij - hiperkalemija - zdravila za zdravljenje hyperkalemia in hyperphosphatemia - zdravilo veltassa je indicirano za zdravljenje hiperkaliemije pri odraslih.

Evropska unija - slovenščina - EMA (European Medicines Agency)

zoetis belgium sa - frunevetmab - analgetiki - mačke - for the alleviation of pain associated with osteoarthritis in cats.

Evropska unija - slovenščina - EMA (European Medicines Agency)

amgen technology (ireland) uc - eculizumab - hemoglobinurija, paroksizmal - imunosupresivi - bekemv is indicated in adults and children for the treatment of paroxysmal nocturnal haemoglobinuria (pnh). dokazila o kliničnih koristi je dokazana pri bolnikih z haemolysis z klinični simptom(i) okvirni visoke aktivnosti bolezni, ne glede na to, transfuzijo zgodovine (glej poglavje 5.

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

actavis group ptc ehf. - risedronska kislina - šumeča zrnca + filmsko obložena tableta - risedronska kislina 32,5 mg / 1 tableta - risedronska kislina, kalcij in holekalciferol, zaporedni

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

bayer d.o.o. - loratadin - sirup - loratadin 1 mg / 1 ml - loratadin

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

alkaloid - int d.o.o. - železo(iii) - peroralna raztopina - železo(iii) 40 mg / 15 ml - železov(iii) proteinsukcinilat

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

alkaloid - int d.o.o. - metadon - peroralna raztopina - metadon 8,95 mg / 1 ml - metadon