Vardenafil Goibela 10 mg Munsönderfallande tablett Ruotsi - ruotsi - Läkemedelsverket (Medical Products Agency)

vardenafil goibela 10 mg munsönderfallande tablett

laboratorios cinfa s.a. - vardenafilhydrokloridtrihydrat - munsönderfallande tablett - 10 mg - vardenafilhydrokloridtrihydrat 11,85 mg aktiv substans; laktosmonohydrat hjälpämne; aspartam hjälpämne

Dupixent Euroopan unioni - ruotsi - EMA (European Medicines Agency)

dupixent

sanofi winthrop industrie - dupilumab - dermatitis, atopic; prurigo; esophageal diseases; asthma; sinusitis - agenter för dermatit, med undantag av 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.

Bosentan Actavis 125 mg Filmdragerad tablett Ruotsi - ruotsi - Läkemedelsverket (Medical Products Agency)

bosentan actavis 125 mg filmdragerad tablett

actavis group ptc ehf. - bosentanmonohydrat - filmdragerad tablett - 125 mg - bosentanmonohydrat 129,082 mg aktiv substans

Bosentan Actavis 62,5 mg Filmdragerad tablett Ruotsi - ruotsi - Läkemedelsverket (Medical Products Agency)

bosentan actavis 62,5 mg filmdragerad tablett

actavis group ptc ehf. - bosentanmonohydrat - filmdragerad tablett - 62,5 mg - bosentanmonohydrat 64,54 mg aktiv substans

Diozi 2,5 mg Filmdragerad tablett Ruotsi - ruotsi - Läkemedelsverket (Medical Products Agency)

diozi 2,5 mg filmdragerad tablett

medical pharmaquality s.a. - tadalafil - filmdragerad tablett - 2,5 mg - laktosmonohydrat hjälpämne; natriumlaurilsulfat hjälpämne; tadalafil 2,5 mg aktiv substans

Diozi 5 mg Filmdragerad tablett Ruotsi - ruotsi - Läkemedelsverket (Medical Products Agency)

diozi 5 mg filmdragerad tablett

medical pharmaquality s.a. - tadalafil - filmdragerad tablett - 5 mg - natriumlaurilsulfat hjälpämne; tadalafil 5 mg aktiv substans; laktosmonohydrat hjälpämne

Diozi 10 mg Filmdragerad tablett Ruotsi - ruotsi - Läkemedelsverket (Medical Products Agency)

diozi 10 mg filmdragerad tablett

medical pharmaquality s.a. - tadalafil - filmdragerad tablett - 10 mg - tadalafil 10 mg aktiv substans; natriumlaurilsulfat hjälpämne; laktosmonohydrat hjälpämne

Diozi 20 mg Filmdragerad tablett Ruotsi - ruotsi - Läkemedelsverket (Medical Products Agency)

diozi 20 mg filmdragerad tablett

medical pharmaquality s.a. - tadalafil - filmdragerad tablett - 20 mg - natriumlaurilsulfat hjälpämne; laktosmonohydrat hjälpämne; tadalafil 20 mg aktiv substans

Dymavig 5 mg Filmdragerad tablett Ruotsi - ruotsi - Läkemedelsverket (Medical Products Agency)

dymavig 5 mg filmdragerad tablett

sigillata ltd - tadalafil - filmdragerad tablett - 5 mg - laktosmonohydrat hjälpämne; tadalafil 5 mg aktiv substans; natriumlaurilsulfat hjälpämne

Dymavig 10 mg Filmdragerad tablett Ruotsi - ruotsi - Läkemedelsverket (Medical Products Agency)

dymavig 10 mg filmdragerad tablett

sigillata ltd - tadalafil - filmdragerad tablett - 10 mg - tadalafil 10 mg aktiv substans; natriumlaurilsulfat hjälpämne; laktosmonohydrat hjälpämne