Cardace Comp 2,5 mg / 12,5 mg tabletti Finlandia - Suomi - Fimea (Suomen lääkevirasto)

cardace comp 2,5 mg / 12,5 mg tabletti

sanofi oy - hydrochlorothiazide, ramipril - tabletti - 2,5 mg / 12,5 mg - ramipriili ja diureetit

Amaryl 1 mg tabletti Finlandia - Suomi - Fimea (Suomen lääkevirasto)

amaryl 1 mg tabletti

sanofi oy - glimepiride - tabletti - 1 mg - glimepiridi

Amaryl 2 mg tabletti Finlandia - Suomi - Fimea (Suomen lääkevirasto)

amaryl 2 mg tabletti

sanofi oy - glimepiride - tabletti - 2 mg - glimepiridi

Klexane Cum Conservans 100 mg/ml injektioneste, liuos Finlandia - Suomi - Fimea (Suomen lääkevirasto)

klexane cum conservans 100 mg/ml injektioneste, liuos

sanofi oy - enoxaparin sodium - injektioneste, liuos - 100 mg/ml - enoksapariini

Cardace 10 mg tabletti Finlandia - Suomi - Fimea (Suomen lääkevirasto)

cardace 10 mg tabletti

sanofi oy - ramipril - tabletti - 10 mg - ramipriili

Dupixent Uni Eropa - 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.

Sarclisa Uni Eropa - Suomi - EMA (European Medicines Agency)

sarclisa

sanofi winthrop industrie - isatuximab - multiple myeloma - antineoplastiset aineet - sarclisa is indicated: in combination with pomalidomide and dexamethasone, for the treatment of adult patients with relapsed and refractory multiple myeloma (mm) who have received at least two prior therapies including lenalidomide and a proteasome inhibitor (pi) and have demonstrated disease progression on the last therapy. in combination with carfilzomib and dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least one prior therapy (see section 5.

Truvelog Mix 30 Uni Eropa - Suomi - EMA (European Medicines Agency)

truvelog mix 30

sanofi winthrop industrie - insuliini aspart - diabetes mellitus - diabeetilla käytettävät lääkkeet - truvelog mix 30 is indicated for treatment of diabetes mellitus in adults, adolescents and children aged 10 years and above.

Enjaymo Uni Eropa - Suomi - EMA (European Medicines Agency)

enjaymo

sanofi b.v. - sutimlimab - hemolysis; anemia, hemolytic, autoimmune - immunosuppressantit - enjaymo is indicated for the treatment of haemolytic anaemia in adult patients with cold agglutinin disease (cad).

Xenpozyme Uni Eropa - Suomi - EMA (European Medicines Agency)

xenpozyme

sanofi b.v. - olipudase alfa - acid sphingomyelinase deficiency (asmd) type a/b or type b - muut ruuansulatuselimistön sairauksien ja aineenvaihduntasairauksien lääkkeet, - xenpozyme is indicated as an enzyme replacement therapy for the treatment of non-central nervous system (cns) manifestations of acid sphingomyelinase deficiency (asmd) in paediatric and adult patients with type a/b or type b.