Belkyra 10 mg/ ml Norge - norsk - Statens legemiddelverk

belkyra 10 mg/ ml

abbvie as - deoksykolsyre - injeksjonsvæske, oppløsning - 10 mg/ ml

Procren Depot 11.25 mg Norge - norsk - Statens legemiddelverk

procren depot 11.25 mg

abbvie as - leuprorelinacetat - pulver og væske til injeksjonsvæske, suspensjon i tokammersprøyte - 11.25 mg

Procren Depot 3.75 mg Norge - norsk - Statens legemiddelverk

procren depot 3.75 mg

abbvie as - leuprorelinacetat - pulver og væske til injeksjonsvæske, suspensjon i tokammersprøyte - 3.75 mg

Procren Depot 30 mg Norge - norsk - Statens legemiddelverk

procren depot 30 mg

abbvie as - leuprorelinacetat - pulver og væske til injeksjonsvæske, suspensjon i tokammersprøyte - 30 mg

Vistabel - Norge - norsk - Statens legemiddelverk

vistabel -

abbvie as - botulinumtoksin type a - pulver til injeksjonsvæske, oppløsning

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

rinvoq

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.

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

aquipta

abbvie deutschland gmbh & co. kg - atogepant - migrene lidelser - aquipta is indicated for prophylaxis of migraine in adults who have at least 4 migraine days per month.

Produodopa 240 mg/ ml / 12 mg/ ml Norge - norsk - Statens legemiddelverk

produodopa 240 mg/ ml / 12 mg/ ml

abbvie as - foslevodopa / foskarbidopa - infusjonsvæske, oppløsning - 240 mg/ ml / 12 mg/ ml

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

nexobrid

mediwound germany gmbh - proteolytic enzymes enriched in bromelain - debridement - preparater for behandling av sår og sår - nexobrid er indikert for fjerning av eschar hos voksne med dype partielle og fullverdige termiske forbrenninger.

Onivyde pegylated liposomal (previously known as Onivyde) Den europeiske union - norsk - EMA (European Medicines Agency)

onivyde pegylated liposomal (previously known as onivyde)

les laboratoires servier - irinotecan anhydrous free-base - bukspyttkjertelblodsykdommer - antineoplastiske midler - behandling av metastatisk adenocarcinoma av bukspyttkjertelen, sammen med 5 fluorouracil (5 fu) og leucovorin (lv), i voksen pasienter som har kommet etter gemcitabine basert terapi.