Evropska unija - slovenščina - EMA (European Medicines Agency)

takeda pharma a/s - vedolizumab - colitis, ulcerative; crohn disease - selektivni imunosupresivi - ulcerozni colitisentyvio je indiciran za zdravljenje odraslih bolnikov z zmerno do močno aktivnim ulceroznim kolitisom, ki so imeli neustreznega odziva, izgubil odgovor da, ali so bili nestrpni, da bodisi konvencionalne terapije ali tumor nekroze faktor alfa (tnfa) antagonist. crohnova diseaseentyvio je indiciran za zdravljenje odraslih bolnikov z zmerno do hudo aktivno crohnovo boleznijo, ki so imeli neustreznega odziva, izgubil odgovor da, ali so bili nestrpni, da bodisi konvencionalne terapije ali tumor nekroze faktor alfa (tnfa) antagonist. pouchitisentyvio is indicated for the treatment of adult patients with moderately to severely active chronic pouchitis, who have undergone proctocolectomy and ileal pouch anal anastomosis for ulcerative colitis, and have had an inadequate response with or lost response to antibiotic therapy.

Evropska unija - slovenščina - EMA (European Medicines Agency)

hansa biopharma ab - imlifidase - desensitization, immunologic; kidney transplantation - imunosupresivi - idefirix is indicated for desensitisation treatment of highly sensitised adult kidney transplant patients with positive crossmatch against an available deceased donor. the use of idefirix should be reserved for patients unlikely to be transplanted under the available kidney allocation system including prioritisation programmes for highly sensitised patients.

Evropska unija - slovenščina - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - deucravacitinib - psoriaza - imunosupresivi - treatment of moderate-to-severe plaque psoriasis in adults.

Evropska unija - slovenščina - EMA (European Medicines Agency)

amgen europe bv - apremilast - arthritis, psoriatic; psoriasis - imunosupresivi - psoriatični arthritisotezla, samostojno ali v kombinaciji z boleznijo spreminjanje antirheumatic drugs (dmards), je primerna za zdravljenje aktivnega psoriatičnega artritisa (psa) pri odraslih bolnikih, ki so imeli ustreznega odgovora, ali ki so bili nestrpni, da pred terapijo dmard. psoriasisotezla je primerna za zdravljenje zmerno do hudo kronično psoriazo v plakih pri odraslih bolnikih, ki odzvali na ali ki so kontraindikacija za, ali so nestrpni do drugih sistemsko terapijo, vključno z ciklosporin, metotreksat ali psoralen in uv-svetlobe (puva).

Evropska unija - slovenščina - EMA (European Medicines Agency)

sanofi b.v. - sutimlimab - hemolysis; anemia, hemolytic, autoimmune - imunosupresivi - enjaymo is indicated for the treatment of haemolytic anaemia in adult patients with cold agglutinin disease (cad).

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

clinigen group plc - koncentrat za raztopino za infundiranje - alemtuzumab

Evropska unija - slovenščina - EMA (European Medicines Agency)

sanofi winthrop industrie - teriflunomide - multiple skleroza - selektivni imunosupresivi - aubagio is indicated for the treatment of adult patients and paediatric patients aged 10 years and older with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 for important information on the population for which efficacy has been established).

Evropska unija - slovenščina - EMA (European Medicines Agency)

sanofi belgium - alemtuzumab - multiple skleroza - selektivni imunosupresivi - lemtrada je indicirano za odraslih bolnikov z recidivno-remitentno multiple skleroze (rrms) z aktivno boleznijo določi kliničnih ali slikanje funkcije.

Evropska unija - slovenščina - EMA (European Medicines Agency)

eli lilly nederland b.v. - baricitinib - artritis, revmatoidni - imunosupresivi - rheumatoid arthritisbaricitinib 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). zdravilo olumiant se lahko uporablja kot monoterapija ali v kombinaciji z metotreksatom. atopic dermatitisolumiant is indicated for the treatment of moderate to severe atopic dermatitis in adult and paediatric patients 2 years of age and older who are candidates for systemic therapy. alopecia areatabaricitinib is indicated for the treatment of severe alopecia areata in adult patients (see section 5. juvenile idiopathic arthritisbaricitinib is indicated for the treatment of active juvenile idiopathic arthritis in patients 2 years of age and older who have had an inadequate response or intolerance to one or more prior conventional synthetic or biologic dmards:- polyarticular juvenile idiopathic arthritis (polyarticular rheumatoid factor positive [rf+] or negative [rf-], extended oligoarticular),- enthesitis related arthritis, and- juvenile psoriatic arthritis. baricitinib may be used as monotherapy or in combination with methotrexate.

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

eli lilly nederland bv - filmsko obložena tableta - baricitinib