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

teysuno

nordic group b.v. - тегафур, gimeracil, oteracil - neoplazme želuca - antineoplastična sredstva - teysuno is indicated in adults:- for the treatment of advanced gastric cancer when given in combination with cisplatin (see section 5. - as monotherapy or in combination with oxaliplatin or irinotecan, with or without bevacizumab, for the treatment of patients with metastatic colorectal cancer for whom it is not possible to continue treatment with another fluoropyrimidine due to hand-foot syndrome or cardiovascular toxicity that developed in the adjuvant or metastatic setting.

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

mvabea

janssen-cilag international n.v.    - recombinant modified vaccinia ankara bavarian nordic virus encoding the: ebola virus zaire (zebov) mayinga strain glycoprotein (gp); ebola virus sudan gulu strain gp; ebola virus taï forest strain nucleoprotein and the marburg virus musoke strain gp - Геморрагическая groznice ebole - cjepiva - active immunization for prevention of disease caused by ebola virus (zaire ebolavirus species) in individuals ≥ 1 year of age.

Veregen 100 mg/g mast Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

veregen 100 mg/g mast

nordic pharma s.r.o., k rybniku 475, jesenice, Češka - ekstrakt lista zelenog čaja - mast - 100 mg/g - urbroj: 1 g masti sadrži 100 mg ekstrakta (u obliku suhog ekstrakta, rafiniranog) camellia sinensis (l.) o. kuntze, folium (list zelenog čaja) (24-56:1), što odgovara: 55-72 mg (-)-epigalokatehingalata: otapalo kod prve ekstracije: voda

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

nordimet

nordic group b.v. - metotreksat - arthritis, psoriatic; psoriasis; arthritis, juvenile rheumatoid; arthritis, rheumatoid - antineoplastična sredstva - nordimet is indicated for the treatment of:active rheumatoid arthritis in adult patients,polyarthritic forms of severe, active juvenile idiopathic arthritis (jia), when the response to nonsteroidal anti-inflammatory drugs (nsaids) has been inadequate,moderate to severe plaque psoriasis in adults who are candidates for systemic therapy, and severe psoriatic arthritis in adult patients, induction of remission in moderate steroid-dependent crohn's disease in adult patients, in combination with corticosteroids and for maintenance of remission, as monotherapy, in patients who have responded to methotrexate.

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

imvanex

bavarian nordic a/s - modificirana vakcina ankara - bavarska nordijska (mva-bn) virus - smallpox vaccine; monkeypox virus - drugih virusnih cjepiva, - active immunisation against smallpox, monkeypox and disease caused by vaccinia virus in adults (see sections 4. 4 i 5. korištenje ovog cjepiva mora se provoditi u skladu sa službenim preporukama.

Rabipur prašak i otapalo za otopinu za injekciju u napunjenoj štrcaljki, cjepivo protiv bjesnoće, inaktivirano Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

rabipur prašak i otapalo za otopinu za injekciju u napunjenoj štrcaljki, cjepivo protiv bjesnoće, inaktivirano

bavarian nordic a/s, philip heymans allé 3, hellerup, danska - virus bjesnoće, soj flury lep (inaktiviran) - prašak i otapalo za otopinu za injekciju u napunjenoj štrcaljki - 1 doza = 1 ml - urbroj: 1 bočica (1,0 ml) nakon rekonstitucije sadrži: virus bjesnoće (inaktivirani, soj flury lep) ≥ 2,5 internacionalne jedinice (iu), proizveden na pročišćenim stanicama pilećih embrija (pcec)

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

bimzelx

ucb pharma s.a.   - bimekizumab - psorijaza - imunosupresivi - plaque psoriasisbimzelx is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritisbimzelx, alone or in combination with methotrexate, is indicated for the treatment of active psoriatic arthritis in adults who have had an inadequate response or who have been intolerant to one or more disease-modifying antirheumatic drugs (dmards). axial spondyloarthritisnon-radiographic axial spondyloarthritis (nr-axspa)bimzelx is indicated for the treatment of adults with active non-radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or magnetic resonance imaging (mri) who have responded inadequately or are intolerant to non-steroidal anti-inflammatory drugs (nsaids). ankylosing spondylitis (as, radiographic axial spondyloarthritis)bimzelx is indicated for the treatment of adults with active ankylosing spondylitis who have responded inadequately or are intolerant to conventional therapy.

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

nuwiq

octapharma ab - simoktookog alfa - hemofilija a - Čimbenici zgrušavanja krvi - liječenje i profilaksu krvarenja u bolesnika s hemofilijom a (nedostatak kongenitalnog faktora viii). nuwiq može se koristiti za sve dobne skupine.

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

vaxchora

bavarian nordic a/s - холерный вибрион, soj i cvd 103-hgr na, živjeti - kolera - cjepiva - vaxchora is indicated for active immunisation against disease caused by vibrio cholerae serogroup o1 in adults and children aged 2 years and older. cjepivo bi trebao biti korišten u skladu sa službenim preporukama.

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

zebinix

bial - portela & ca, s.a. - eslikarbazepin acetat - epilepsija - antiepileptici sredstva, - zebinix je indiciran kao pomoćna terapija kod odraslih, adolescenata i djece iznad 6 godina, s parcijalnim napadajima sa ili bez sekundarne generalizacije.