Suomi -
suomi -
Fimea (Suomen lääkevirasto)
pulmonox awo 0.1 % lääkkeellinen kaasu, puristettu
woikoski oy - nitric oxide - lääkkeellinen kaasu, puristettu - 0.1 % - typpioksidi
Euroopan unioni -
suomi -
EMA (European Medicines Agency)
inomax
linde healthcare ab - typpioksidi - hypertension, pulmonary; respiratory insufficiency - muut hengitysteiden tuotteet - inomax, yhdessä potilaan hengityksen tukeminen ventilaation avulla ja muita asianmukaisia aktiivisia aineita, on ilmoitettu:hoitoon vastasyntyneiden ≥34 raskausviikolla kanssa hypoksinen hengityksen vajaatoiminta ja siihen liittyviä kliinisiä tai kaikukardiografisia todisteita pulmonaalihypertensiosta, jotta voidaan parantaa hapetusta ja vähentää tarvetta ecmo;osana hoito peri - ja postoperatiivisen pulmonaalihypertension hoidossa aikuisilla ja vastasyntyneet, imeväisikäiset ja pikkulapset, lapset ja nuoret, iältään 0-17 vuotta yhdessä sydänkirurgia, jotta valikoivasti vähentää keuhkovaltimon painetta ja parantamaan oikean kammion toimintaa ja hapetusta.
Euroopan unioni -
suomi -
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.
Euroopan unioni -
suomi -
EMA (European Medicines Agency)
tezspire
astrazeneca ab - tezepelumab - astma - obstruktiivisten hengitystiesairauksien lääkkeet, - tezspire is indicated as an add-on maintenance treatment in adults and adolescents 12 years and older with severe asthma who are inadequately controlled despite high dose inhaled corticosteroids plus another medicinal product for maintenance treatment.