MOMETASONE STADA 50 mikrog/annos nenäsumute, suspensio Finlandia - fiński - Fimea (Suomen lääkevirasto)

mometasone stada 50 mikrog/annos nenäsumute, suspensio

stada arzneimittel ag - mometasoni furoas monohydricus - nenäsumute, suspensio - 50 mikrog/annos - mometasoni

Dupixent Unia Europejska - fiński - EMA (European Medicines Agency)

dupixent

sanofi winthrop industrie - dupilumab - dermatitis, atopic; prurigo; esophageal diseases; asthma; sinusitis - dermatiittiautia lukuun ottamatta kortikosteroideja - 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.

Sendolor 1 mg/ml infuusioneste, liuos Finlandia - fiński - Fimea (Suomen lääkevirasto)

sendolor 1 mg/ml infuusioneste, liuos

eurocept international bv - morphine hydrochloride trihydrate - infuusioneste, liuos - 1 mg/ml - morfiini

Sendolor 10 mg/ml infuusioneste, liuos Finlandia - fiński - Fimea (Suomen lääkevirasto)

sendolor 10 mg/ml infuusioneste, liuos

eurocept international bv - morphine hydrochloride trihydrate - infuusioneste, liuos - 10 mg/ml - morfiini

Sendolor 20 mg/ml infuusioneste, liuos Finlandia - fiński - Fimea (Suomen lääkevirasto)

sendolor 20 mg/ml infuusioneste, liuos

eurocept international bv - morphine hydrochloride trihydrate - infuusioneste, liuos - 20 mg/ml - morfiini

Sendolor 1 mg/ml injektioneste, liuos Finlandia - fiński - Fimea (Suomen lääkevirasto)

sendolor 1 mg/ml injektioneste, liuos

eurocept international bv - morphine hydrochloride trihydrate - injektioneste, liuos - 1 mg/ml - morfiini

Sendolor 10 mg/ml injektioneste, liuos Finlandia - fiński - Fimea (Suomen lääkevirasto)

sendolor 10 mg/ml injektioneste, liuos

eurocept international bv - morphine hydrochloride trihydrate - injektioneste, liuos - 10 mg/ml - morfiini

Sendolor 20 mg/ml injektioneste, liuos Finlandia - fiński - Fimea (Suomen lääkevirasto)

sendolor 20 mg/ml injektioneste, liuos

eurocept international bv - morphine hydrochloride trihydrate - injektioneste, liuos - 20 mg/ml - morfiini

Bimzelx Unia Europejska - fiński - EMA (European Medicines Agency)

bimzelx

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