Norge - norsk - Statens legemiddelverk

2care4 aps - gentamicinsulfat - infusjonsvæske, oppløsning - 3 mg/ ml

Norge - norsk - Statens legemiddelverk

2care4 aps - gentamicinsulfat - infusjonsvæske, oppløsning - 3 mg/ ml

Norge - norsk - Statens legemiddelverk

eurocept international b.v - tobramycinsulfat - injeksjonsvæske, oppløsning - 40 mg/ ml

Norge - norsk - Statens legemiddelverk

xellia pharmaceuticals a. p. s - vankomycinhydroklorid - pulver til infusjonsvæske, oppløsning - 500 mg

Norge - norsk - Statens legemiddelverk

ethypharm (1) - suksametoniumkloriddihydrat - injeksjons-/infusjonsvæske, oppløsning - 50 mg/ ml

Den europeiske union - norsk - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - upadacitinib - leddgikt, reumatoid - immunsuppressive - 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.

Den europeiske union - norsk - EMA (European Medicines Agency)

shionogi b.v. - cefiderocol sulfat tosilate - gram-negative bakterielle infeksjoner - antibakterielle midler for systemisk bruk, - fetcroja er angitt for behandling av infeksjoner forårsaket av aerobe, gram-negative organismer i voksne med begrenset behandlingstilbud (se kapittel 4. 2, 4. 4 og 5. det bør vurderes å offisielle retningslinjer for riktig bruk av antibakterielle midler.

Den europeiske union - norsk - EMA (European Medicines Agency)

gilead sciences ireland uc, galapagos nv - filgotinib maleate - leddgikt, reumatoid - immunsuppressive - rheumatoid arthritisjyseleca 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). jyseleca may be used as monotherapy or in combination with methotrexate (mtx). ulcerative colitisjyseleca is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a biologic agent.

Norge - norsk - Statens legemiddelverk

laboratoire aguettant - suksametoniumkloriddihydrat - injeksjonsvæske, oppløsning i ferdigfylt sprøyte - 10 mg/ ml

Norge - norsk - Statens legemiddelverk

chanelle pharmaceuticals manufacturing ltd - mikonazolnitrat / prednisolonacetat / polymyksin b sulfat - Øredråper, suspensjon - 23 mg/ ml / 5 mg/ ml / 5500 ie/ ml