Cancidas (previously Caspofungin MSD) Evropska unija - slovenščina - EMA (European Medicines Agency)

cancidas (previously caspofungin msd)

merck sharp & dohme b.v. - caspofungin (as acetate) - candidiasis; aspergillosis - antimikotiki za sistemsko uporabo - treatment of invasive candidiasis in adult or paediatric patients;treatment of invasive aspergillosis in adult or paediatric patients who are refractory to or intolerant of amphotericin b, lipid formulations of amphotericin b and / or itraconazole. refractoriness is defined as progression of infection or failure to improve after a minimum of seven days of prior therapeutic doses of effective antifungal therapy;empirical therapy for presumed fungal infections (such as candida or aspergillus) in febrile, neutropaenic adult or paediatric patients.

Rinvoq Evropska unija - slovenščina - EMA (European Medicines Agency)

rinvoq

abbvie deutschland gmbh & co. kg - upadacitinib - artritis, revmatoidni - imunosupresivi - rheumatoid arthritisrinvoq is indicated for the treatment of moderate to severe active rheumatoid arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more disease-modifying anti-rheumatic drugs (dmards). rinvoq may be used as monotherapy or in combination with methotrexate. psoriatic arthritisrinvoq is indicated for the treatment of active psoriatic arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more dmards. rinvoq may be used as monotherapy or in combination with methotrexate. axial spondyloarthritisnon-radiographic axial spondyloarthritis (nr-axspa)rinvoq is indicated for the treatment of active non-radiographic axial spondyloarthritis in adult patients with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or magnetic resonance imaging (mri), who have responded inadequately to nonsteroidal anti-inflammatory drugs (nsaids). ankylosing spondylitis (as, radiographic axial spondyloarthritis)rinvoq is indicated for the treatment of active ankylosing spondylitis in adult patients who have responded inadequately to conventional therapy. atopic dermatitisrinvoq is indicated for the treatment of moderate to severe atopic dermatitis in adults and adolescents 12 years and older who are candidates for systemic therapy. ulcerative colitisrinvoq is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response, lost response or were intolerant to either conventional therapy or a biologic agent.  crohn’s diseaserinvoq is indicated for the treatment of adult patients with moderately to severely active crohn’s disease who have had an inadequate response, lost response or were intolerant to either conventional therapy or a biologic agent.

Reyataz Evropska unija - slovenščina - EMA (European Medicines Agency)

reyataz

bristol-myers squibb pharma eeig - atazanavir (as sulfate) - okužbe z virusom hiv - antivirusi za sistemsko uporabo - reyataz kapsule, skupaj upravlja z majhnim odmerkom ritonavirja, so navedene za zdravljenje hiv-1 okuženih odraslih in pediatričnih bolnikov 6 let in starejših v kombinaciji z drugimi protiretrovirusna zdravila, (glej oddelek 4. na podlagi razpoložljivih virological in kliničnih podatkov odraslih bolnikih, nobene koristi ni pričakovati pri bolnikih s sevi, odporni na več protease inhibitorji (≥ 4 pi mutacije). izbira reyataz v zdravljenje izkušenih odraslih in pediatričnih bolnikih mora temeljiti na posameznih virusnih odpornost testiranje in bolnika v zdravljenje zgodovine (glej točki 4. 4 in 5. reyataz ustno v prahu, co-daje z nizkim odmerkom ritonavir, je navedeno v kombinaciji z drugimi protiretrovirusnimi zdravili za zdravljenje okužbe z virusom hiv-1 okuženih pediatrični bolniki vsaj 3 mesece starosti, ki tehta vsaj 5 kg (glejte poglavje 4. na podlagi razpoložljivih virological in kliničnih podatkov odraslih bolnikih, nobene koristi ni pričakovati pri bolnikih s sevi, odporni na več protease inhibitorji ( 4 pi mutacije). izbira reyataz v zdravljenje izkušenih odraslih in pediatričnih bolnikih mora temeljiti na posameznih virusnih odpornost testiranje in bolnika v zdravljenje zgodovine (glej točki 4. 4 in 5.

Triumeq Evropska unija - slovenščina - EMA (European Medicines Agency)

triumeq

viiv healthcare b.v. - dolutegravir sodium, lamivudine, abacavir (as sulfate) - okužbe z virusom hiv - antivirusi za sistemsko uporabo - triumeq is indicated for the treatment of human immunodeficiency virus (hiv) infected adults,  adolescents and children  weighing at least 25 kg who are antiretroviral treatment-naïve or are infected with hiv without documented or clinically suspected resistance to any of the three antiretroviral agents in triumeq.

Chenodeoxycholic acid Leadiant (previously known as Chenodeoxycholic acid sigma-tau) Evropska unija - slovenščina - EMA (European Medicines Agency)

chenodeoxycholic acid leadiant (previously known as chenodeoxycholic acid sigma-tau)

leadiant gmbh - chenodeoxycholic kisline - xanthomatosis, cerebrotendinous; metabolism, inborn errors - terapija z jetri in jeter - chenodeoxycholic kislina je indiciran za zdravljenje prirojenih napak primarni žolčnih kislin sinteze zaradi sterola 27 hidroksilaza pomanjkljivosti (predstavlja kot cerebrotendinous xanthomatosis (ctx)) pri dojenčkih, otrocih in mladostnikih, starih od 1 mesec do 18 let in odrasli.