Rosix Duo 20 mg/100 mg tvrde kapsule Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

rosix duo 20 mg/100 mg tvrde kapsule

belupo lijekovi i kozmetika d.d., ulica danica 5, koprivnica, hrvatska - rosuvastatinkalcij acetilsalicilatna kiselina - kapsula, tvrda - 20 mg + 100 mg - urbroj: jedna tvrda kapsula sadrži 20 mg rosuvastatina (u obliku rosuvastatin kalcija) i 100 mg acetilsalicilatne kiseline

Rosix Duo 5 mg/100 mg tvrde kapsule Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

rosix duo 5 mg/100 mg tvrde kapsule

belupo lijekovi i kozmetika d.d., ulica danica 5, koprivnica, hrvatska - rosuvastatinkalcij acetilsalicilatna kiselina - kapsula, tvrda - 5 mg + 100 mg - urbroj: jedna tvrda kapsula sadrži 5 mg rosuvastatina (u obliku rosuvastatin kalcija) i 100 mg acetilsalicilatne kiseline

Jayempi Europska Unija - hrvatski - EMA (European Medicines Agency)

jayempi

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.

Krystexxa Europska Unija - hrvatski - EMA (European Medicines Agency)

krystexxa

crealta pharmaceuticals ireland limited - pegloticase - giht - antigadni pripravci - krystexxa je indiciran za liječenje teškog oslabiti kronične tophaceous gihta u odraslih bolesnika koji može imati erozivni zajednički angažman i koji nisu uspjeli normalizirati serumske mokraćne kiseline s ksantin oksidaza inhibitori maksimalno medicinski odgovarajuće doze ili kojima ovi lijekovi su kontraindicirani.

Duzallo Europska Unija - hrvatski - EMA (European Medicines Agency)

duzallo

grunenthal gmbh - allopurinol, lesinurad - giht - antigadni pripravci - duzallo prikazan kod odraslih za liječenje hiperurikemijom u bolesnika s giht, koji još nije ostvarila ciljane razine mokraćne kiseline u serumu uz odgovarajuću dozu Аллопуринола sami.

Descovy Europska Unija - hrvatski - EMA (European Medicines Agency)

descovy

gilead sciences ireland uc - эмтрицитабин, Тенофовир alafenamide - hiv infekcije - antivirusni lijekovi za sustavnu uporabu - descovy is indicated in combination with other antiretroviral agents for the treatment of adults and adolescents (aged 12 years and older with body weight at least 35 kg) infected with human immunodeficiency virus type 1 (hiv-1).

Genvoya Europska Unija - hrvatski - EMA (European Medicines Agency)

genvoya

gilead sciences ireland uc - элвитегравир, кобицистат, эмтрицитабин, Тенофовир alafenamide - hiv infekcije - antivirusni lijekovi za sustavnu uporabu - genvoya je indiciran za liječenje odraslih i adolescenata (u dobi od 12 godina i stariji sa tjelesne težine najmanje 35 kg) zaraženih virusom humane imunodeficijencije (hiv-a 1) 1 bez bilo koje poznate mutacija povezanih s rezistencijom na inhibitora integraze, emtricitabin ili tenofovir.