Vancomycin "CNP" 1000 mg pulver til infusionsvæske, opløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

vancomycin "cnp" 1000 mg pulver til infusionsvæske, opløsning

cnp pharma gmbh - vancomycinhydrochlorid - pulver til infusionsvæske, opløsning - 1000 mg

Vancomycin "CNP" 500 mg pulver til infusionsvæske, opløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

vancomycin "cnp" 500 mg pulver til infusionsvæske, opløsning

cnp pharma gmbh - vancomycinhydrochlorid - pulver til infusionsvæske, opløsning - 500 mg

Voxzogo Den Europæiske Union - dansk - EMA (European Medicines Agency)

voxzogo

biomarin international limited - vosoritide - achondroplasia - narkotika til behandling af knoglesygdomme - voxzogo is indicated for the treatment of achondroplasia in patients 4 months of age and older whose epiphyses are not closed. the diagnosis of achondroplasia should be confirmed by appropriate genetic testing.

Dupixent Den Europæiske Union - dansk - EMA (European Medicines Agency)

dupixent

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.

Capex Suspensionskoncentrat Danmark - dansk - SEGES Landbrug & Fødevarer

capex suspensionskoncentrat

andermatt biocontrol ag - adoxophyes - suspensionskoncentrat - 10 g/l adoxophyes orana granulose virus

Madex Top Suspensionskoncentrat Danmark - dansk - SEGES Landbrug & Fødevarer

madex top suspensionskoncentrat

borregaard bioplant - cydia - suspensionskoncentrat - 10 g/l cydia pomonella granulosis virus (cpgv)

Buprenorphin/Naloxon "G.L. Pharma" 8+2 mg resoribletter, sublinguale Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

buprenorphin/naloxon "g.l. pharma" 8+2 mg resoribletter, sublinguale

g.l. pharma gmbh - buprenorphinhydrochlorid, naloxonhydrochloriddihydrat - resoribletter, sublinguale - 8+2 mg

Buprenorphin/Naloxon "G.L. Pharma" 2+0,5 mg resoribletter, sublinguale Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

buprenorphin/naloxon "g.l. pharma" 2+0,5 mg resoribletter, sublinguale

g.l. pharma gmbh - buprenorphinhydrochlorid, naloxonhydrochloriddihydrat - resoribletter, sublinguale - 2+0,5 mg

Pregabalin Sandoz GmbH Den Europæiske Union - dansk - EMA (European Medicines Agency)

pregabalin sandoz gmbh

sandoz gmbh - pregabalin - anxiety disorders; epilepsy - antiepileptika, - epilepsypregabalin sandoz gmbh er indiceret som adjuverende behandling til voksne med partielle anfald med eller uden sekundær generalisering. generaliseret angst disorderpregabalin sandoz gmbh er indiceret til behandling af generaliseret angst (gad) hos voksne.