Latvija - latviešu - Zāļu valsts aģentūra

perrigo romania srl, romania - paracetamolum, codeini phosphas hemihydricus, kofeīns - tablete - 500 mg/8 mg/30 mg

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

laboratoire hra pharma - ulipristal - kontracepcija, postcoital - dzimumhormoni un dzimumsistēmas modulatori dzimumorgānu sistēmas, , avārijas kontracepcijas līdzekļi - Ārkārtas kontracepcija 120 stundu laikā (piecās dienās) no neaizsargāta dzimumakta vai kontracepcijas līdzekļa mazspējas.

Latvija - latviešu - Pārtikas un veterinārais dienests, Zemkopības ministrija

perrigo holland - tablete

Latvija - latviešu - Zāļu valsts aģentūra

ranbaxy (poland) sp.z.o.o., poland - ksilometazolīna hidrohlorīds - deguna aerosols, šķīdums - 0,5 mg/ml

Latvija - latviešu - Zāļu valsts aģentūra

ranbaxy (poland) sp.z.o.o., poland - ksilometazolīna hidrohlorīds - deguna aerosols, šķīdums - 1 mg/ml

Latvija - latviešu - Zāļu valsts aģentūra

biologische heilmittel heel gmbh, germany - conium plankumainas, ambra grisea, un naftas rectificatum, anamirta cocculus - tablete

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

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.

Latvija - latviešu - Zāļu valsts aģentūra

teva pharma b.v., netherlands - kandesartāna cileksetils - tablete - 16 mg

Latvija - latviešu - Zāļu valsts aģentūra

teva pharma b.v., netherlands - candesartanum cilexetilum, hydrochlorothiazidum - tablete - 16 mg/12,5 mg

Latvija - latviešu - Zāļu valsts aģentūra

us pharmacia sp. z o.o., poland - paracetamols - suspensija iekšķīgai lietošanai - 40 mg/ml