Berinert 2000 IU Nórsko - nórčina - Statens legemiddelverk

berinert 2000 iu

csl behring gmbh (2) - c1-esteraseinhibitor, human - pulver og væske til injeksjonsvæske, oppløsning - 2000 iu

Imcivree Európska únia - nórčina - EMA (European Medicines Agency)

imcivree

rhythm pharmaceuticals netherlands b.v. - setmelanotide - fedme - antiobesity preparater, ekskl. diettprodukter - imcivree is indicated for the treatment of obesity and the control of hunger associated with genetically confirmed bardet biedl syndrome (bbs), loss-of-function biallelic pro-opiomelanocortin (pomc), including pcsk1, deficiency or biallelic leptin receptor (lepr) deficiency in adults and children 6 years of age and above.

Drovelis Európska únia - nórčina - EMA (European Medicines Agency)

drovelis

gedeon richter plc. - drospirenone, estetrol monohydrate - contraceptives, oral - sex hormoner og modulatorer av genital systemet, - oral contraceptive.

Lydisilka Európska únia - nórčina - EMA (European Medicines Agency)

lydisilka

estetra sprl - estetrol monohydrate, drospirenone - contraceptives, oral - sex hormoner og modulatorer av genital systemet, - oral prevensjon. the decision to prescribe lydisilka should take into consideration the individual woman’s current risk factors, particularly those for venous thromboembolism (vte), and how the risk of vte with lydisilka compares with other combined hormonal contraceptives (chcs) (see sections 4. 3 and 4.

Voxzogo Európska únia - nórčina - EMA (European Medicines Agency)

voxzogo

biomarin international limited - vosoritide - achondroplasia - legemidler til behandling av bein sykdommer - voxzogo is indicated for the treatment of achondroplasia in patients 4 months of age and older whose epiphyses are not closed. the diagnosis of achondroplasia should be confirmed by appropriate genetic testing.

Bimzelx Európska únia - nórčina - EMA (European Medicines Agency)

bimzelx

ucb pharma s.a.   - bimekizumab - psoriasis - immunsuppressive - 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.

Vaxneuvance Európska únia - nórčina - EMA (European Medicines Agency)

vaxneuvance

merck sharp & dohme b.v.  - pneumococcal polysaccharide conjugate vaccine (adsorbed) - pneumokokkerinfeksjoner - pneumococcus, purified polysaccharides antigen conjugated - vaxneuvance is indicated for active immunisation for the prevention of invasive disease, pneumonia and acute otitis media caused by streptococcus pneumoniae in infants, children and adolescents from 6 weeks to less than 18 years of age. vaxneuvance is indicated for active immunisation for the prevention of invasive disease and pneumonia caused by streptococcus pneumoniae in individuals 18 years of age and older. se avsnitt 4. 4 og 5. 1 for informasjon om beskyttelse mot spesifikke pneumokokserotyper. the use of vaxneuvance should be in accordance with official recommendations.

Ablavar (previously Vasovist) Európska únia - nórčina - EMA (European Medicines Agency)

ablavar (previously vasovist)

tmc pharma services ltd. - gadofosvesetriatrium - magnetic resonance angiography - kontrastmedier - dette legemidlet er kun til diagnostisk bruk. ablavar er indikert for kontrast-forsterket magnetisk resonans angiografi (ce-mra) for visualisering av abdominal eller lem fartøy i kun for voksne, med mistenkt eller kjent for vaskulær sykdom.

Actraphane Európska únia - nórčina - EMA (European Medicines Agency)

actraphane

novo nordisk a/s - insulin human - sukkersyke - legemidler som brukes i diabetes - behandling av diabetes mellitus.

Actrapid Európska únia - nórčina - EMA (European Medicines Agency)

actrapid

novo nordisk a/s - humant insulin - sukkersyke - legemidler som brukes i diabetes - behandling av diabetes mellitus.