Levofloxacin Claris 5 mg/ml šķīdums infūzijām Latvija - latviešu - Zāļu valsts aģentūra

levofloxacin claris 5 mg/ml šķīdums infūzijām

claris lifesciences (uk) limited, united kingdom - levofloksacīns - Šķīdums infūzijām - 5 mg/ml

Clariscan 0,5 mmol/ml šķīdums injekcijām Latvija - latviešu - Zāļu valsts aģentūra

clariscan 0,5 mmol/ml šķīdums injekcijām

ge healthcare as, norway - gadoterskābe - Šķīdums injekcijām - 0,5 mmol/ml

Clariscan 0,5 mmol/ml šķīdums injekcijām pilnšļircē Latvija - latviešu - Zāļu valsts aģentūra

clariscan 0,5 mmol/ml šķīdums injekcijām pilnšļircē

ge healthcare as, norway - gadoterskābe - Šķīdums injekcijām pilnšļircē - 0,5 mmol/ml

Seclaris DC Latvija - latviešu - Pārtikas un veterinārais dienests, Zemkopības ministrija

seclaris dc

ceva sante animale,, francija - cefalonijs - suspensija ievadīšanai tesmenī - 250 mg - cietstāvošas govis

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.

Sapropterin Dipharma Eiropas Savienība - latviešu - EMA (European Medicines Agency)

sapropterin dipharma

dipharma arzneimittel gmbh - sapropterīna dihidrohlorīds - fenilketonūrias - citas gremošanas trakta un metabolisma produkti, - sapropterin dipharma is indicated for the treatment of hyperphenylalaninaemia (hpa) in adults and paediatric patients of all ages with phenylketonuria (pku) who have been shown to be responsive to such treatment. sapropterin dipharma is also indicated for the treatment of hyperphenylalaninaemia (hpa) in adults and paediatric patients of all ages with tetrahydrobiopterin (bh4) deficiency who have been shown to be responsive to such treatment.

OLIMEL N9E emulsija infūzijām Latvija - latviešu - Zāļu valsts aģentūra

olimel n9e emulsija infūzijām

baxter s.a., belgium - olīveļļa raffinatum, soiae naftas raffinatum, alaninum, argininum, skābes asparticum, skābes glutamicum, glycinum, histidinum, isoleucinum, leucinum, lysinum, methioninum, phenylalaninum, prolinum, serinum, threoninum, tryptophanum, tyrosinum, valinum, natrii acetas trihydricus, natrii glycerophosphas, kalii chloridum, magnija chloridum hexahydricum, kalcija chloridum dihydricum, glikozes monohydricum - emulsija infūzijām

OLIMEL N7E emulsija infūzijām Latvija - latviešu - Zāļu valsts aģentūra

olimel n7e emulsija infūzijām

baxter s.a., belgium - olīveļļa raffinatum, soiae naftas raffinatum, alaninum, argininum, skābes asparticum, skābes glutamicum, glycinum, histidinum, isoleucinum, leucinum, lysinum, methioninum, phenylalaninum, prolinum, serinum, threoninum, tryptophanum, tyrosinum, valinum, natrii acetas trihydricus, natrii glycerophosphas, kalii chloridum, magnija chloridum hexahydricum, kalcija chloridum dihydricum, glikozes monohydricum - emulsija infūzijām