Avrupa Birliği - Norveççe - EMA (European Medicines Agency)

pfizer europe ma eeig - tafamidis - amyloidosis - andre nervesystemet narkotika - vyndaqel er indisert for behandling av transthyretinamyloidose hos voksne pasienter med fase 1-symptomatisk polyneuropati for å forsinke perifer neurologisk nedsatt funksjonsevne.

Avrupa Birliği - Norveççe - EMA (European Medicines Agency)

sanofi winthrop industrie - sarilumab - leddgikt, reumatoid - immunsuppressive - kevzara i kombinasjon med methotrexate (mtx) er indisert for behandling av moderat til alvorlig aktive revmatoid artritt (ra) hos voksne pasienter som har svart mangelfullt på, eller som er intolerante for én eller flere sykdom endre anti revmatiske narkotika (dmards). kevzara kan gis som monoterapi ved intoleranse mot mtx eller når behandling med mtx er upassende.

Avrupa Birliği - Norveççe - EMA (European Medicines Agency)

sanofi winthrop industrie - dupilumab - dermatitis, atopic; prurigo; esophageal diseases; asthma; sinusitis - agenter for dermatitt, unntatt kortikosteroider - atopic dermatitisadults and adolescentsdupixent 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. children 6 months to 11 years of agedupixent is indicated for the treatment of severe atopic dermatitis in children 6 months to 11 years old who are candidates for systemic therapy. asthmaadults and adolescentsdupixent is indicated in adults and adolescents 12 years and older as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (feno), see section 5. 1, who are inadequately controlled with high dose inhaled corticosteroids (ics) plus another medicinal product for maintenance treatment. children 6 to 11 years of agedupixent is indicated in children 6 to 11 years old as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (feno), who are inadequately controlled with medium to high dose inhaled corticosteroids (ics) plus another medicinal product for maintenance treatment. chronic rhinosinusitis with nasal polyposis (crswnp)dupixent is indicated as an add-on therapy with intranasal corticosteroids for the treatment of adults with severe crswnp for whom therapy with systemic corticosteroids and/or surgery do not provide adequate disease control. prurigo nodularis (pn)dupixent is indicated for the treatment of adults with moderate-to-severe prurigo nodularis (pn) who are candidates for systemic therapy. eosinophilic esophagitis (eoe)dupixent is indicated for the treatment of eosinophilic esophagitis in adults and adolescents 12 years and older, weighing at least 40 kg, who are inadequately controlled by, are intolerant to, or who are not candidates for conventional medicinal therapy.

Norveç - Norveççe - Statens legemiddelverk

orion corporation orion pharma - medetomidinhydroklorid - injeksjonsvæske, oppløsning - 1 mg/ ml

Norveç - Norveççe - Statens legemiddelverk

bracco imaging spa - gadobenatdimeglumin - injeksjonsvæske, oppløsning - 334 mg/ ml

Norveç - Norveççe - Statens legemiddelverk

bracco imaging spa - gadobenatdimeglumin - injeksjonsvæske, oppløsning - 334 mg/ ml

Avrupa Birliği - Norveççe - EMA (European Medicines Agency)

teva gmbh - fremanezumab - migrene lidelser - calcitonin gene-related peptide (cgrp) antagonists - ajovy er indisert for profylakse av migrene hos voksne som har minst 4 migrene dager per måned.

Norveç - Norveççe - Statens legemiddelverk

csl behring gmbh (2) - c1-esteraseinhibitor, human - pulver og væske til injeksjonsvæske, oppløsning - 3000 iu

Norveç - Norveççe - Statens legemiddelverk

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

Avrupa Birliği - Norveççe - EMA (European Medicines Agency)

novartis europharm limited - crizanlizumab - anemi, sickle cell - other hematological agents - adakveo is indicated for the prevention of recurrent vaso occlusive crises (vocs) in sickle cell disease patients aged 16 years and older. it can be given as an add on therapy to hydroxyurea/hydroxycarbamide (hu/hc) or as monotherapy in patients for whom hu/hc is inappropriate or inadequate.