Vancomycin CNP 500 mg pulveris infūziju šķīduma pagatavošanai Latvija - latviešu - Zāļu valsts aģentūra

vancomycin cnp 500 mg pulveris infūziju šķīduma pagatavošanai

cnp pharma gmbh, germany - vankomicīns - pulveris infūziju šķīduma pagatavošanai - 500 mg

Vancomycin CNP 1000 mg pulveris infūziju šķīduma pagatavošanai Latvija - latviešu - Zāļu valsts aģentūra

vancomycin cnp 1000 mg pulveris infūziju šķīduma pagatavošanai

cnp pharma gmbh, germany - vankomicīns - pulveris infūziju šķīduma pagatavošanai - 1000 mg

Voxzogo Eiropas Savienība - latviešu - EMA (European Medicines Agency)

voxzogo

biomarin international limited - vosoritide - achondroplasia - zāles kaulu slimību ārstēšanai - 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 Eiropas Savienība - latviešu - EMA (European Medicines Agency)

dupixent

sanofi winthrop industrie - dupilumabs - dermatitis, atopic; prurigo; esophageal diseases; asthma; sinusitis - agents for dermatitis, excluding corticosteroids - 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.

Imipenem/Cilastatin Venus Pharma 500 mg/500 mg pulveris infūziju šķīduma pagatavošanai Latvija - latviešu - Zāļu valsts aģentūra

imipenem/cilastatin venus pharma 500 mg/500 mg pulveris infūziju šķīduma pagatavošanai

venus pharma gmbh, germany - imipenemum, cilastatinum - pulveris infūziju šķīduma pagatavošanai - 500 mg/500 mg

Imipenem + Cilastatina Venus Pharma 500 mg + 500 mg pulveris infūziju šķīduma pagatavošanai Latvija - latviešu - Zāļu valsts aģentūra

imipenem + cilastatina venus pharma 500 mg + 500 mg pulveris infūziju šķīduma pagatavošanai

venus pharma gmbh, germany - imipenemum, cilastatinum - pulveris infūziju šķīduma pagatavošanai - 500 mg/500 mg

Colpermin 187 mg zarnās šķīstošās cietās kapsulas Latvija - latviešu - Zāļu valsts aģentūra

colpermin 187 mg zarnās šķīstošās cietās kapsulas

tillotts pharma gmbh, germany - menthae piperitae aetheroleum - zarnās šķīstošā kapsula, cietā - 187 mg

Methadone G.L.Pharma 10 mg/ml koncentrāts iekšķīgi lietojama šķīduma pagatavošanai Latvija - latviešu - Zāļu valsts aģentūra

methadone g.l.pharma 10 mg/ml koncentrāts iekšķīgi lietojama šķīduma pagatavošanai

g.l. pharma gmbh, austria - metadona hidrohlorīds - koncentrāts iekšķīgi lietojama šķīduma pagatavošanai - 10 mg/ml

Levomethadone G.L.Pharma 5 mg/ml koncentrāts iekšķīgi lietojama šķīduma pagatavošanai Latvija - latviešu - Zāļu valsts aģentūra

levomethadone g.l.pharma 5 mg/ml koncentrāts iekšķīgi lietojama šķīduma pagatavošanai

g.l. pharma gmbh, austria - levometadona hidrohlorīds - koncentrāts iekšķīgi lietojama šķīduma pagatavošanai - 5 mg/ml