Dania - duński - Lægemiddelstyrelsen (Danish Medicines Agency)

europharma.dk aps - risperidon - depotinjektionsvæske, pulver og solvens til suspension - 37,5 mg

Dania - duński - Lægemiddelstyrelsen (Danish Medicines Agency)

abacus medicine a/s - risperidon - depotinjektionsvæske, pulver og solvens til suspension - 50 mg

Dania - duński - Lægemiddelstyrelsen (Danish Medicines Agency)

orifarm a/s - risperidon - depotinjektionsvæske, pulver og solvens til suspension - 50 mg

Dania - duński - Lægemiddelstyrelsen (Danish Medicines Agency)

2care4 aps - risperidon - depotinjektionsvæske, pulver og solvens til suspension - 50 mg

Dania - duński - Lægemiddelstyrelsen (Danish Medicines Agency)

europharma.dk aps - risperidon - depotinjektionsvæske, pulver og solvens til suspension - 50 mg

Unia Europejska - duński - EMA (European Medicines Agency)

sanofi winthrop industrie - dupilumab - dermatitis, atopic; prurigo; esophageal diseases; asthma; sinusitis - midler til dermatitis, undtagen 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.

Dania - duński - Lægemiddelstyrelsen (Danish Medicines Agency)

2care4 aps - clarithromycin - granulat til oral suspension - 50 mg/ml

Dania - duński - Lægemiddelstyrelsen (Danish Medicines Agency)

2care4 generics aps - amoxicillintrihydrat - pulver til oral suspension - 50 mg/ml

Unia Europejska - duński - EMA (European Medicines Agency)

sanofi belgium - alemtuzumab - multipel sclerose - selektive immunosuppressiva - lemtrada er indiceret til voksne patienter med recidiverende remitterende multipel sklerose (rrms) med aktiv sygdom defineret ved kliniske eller billeddannende egenskaber.

Dania - duński - Lægemiddelstyrelsen (Danish Medicines Agency)

2care4 aps - amoxicillintrihydrat, kaliumclavulanat - pulver til oral suspension - 50 mg/ml+12,5 mg/ml