الاتحاد الأوروبي - اللاتفية - EMA (European Medicines Agency)

moderna biotech spain, s.l. - single-stranded, 5’-capped messenger rna (mrna) produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - vakcīnas - spikevax is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older. spikevax bivalent original/omicron ba. 1 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 years of age and older who have previously received at least a primary vaccination course against covid-19. spikevax bivalent original/omicron ba. 4-5 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older.  spikevax xbb. 5 is indicated for active immunisation to prevent covid 19 caused by sars-cov-2 in individuals 6 months of age and older. the use of this vaccine should be in accordance with official recommendations.

لاتفيا - اللاتفية - Pārtikas un veterinārais dienests, Zemkopības ministrija

kapsula

لاتفيا - اللاتفية - Pārtikas un veterinārais dienests, Zemkopības ministrija

kapsula

الاتحاد الأوروبي - اللاتفية - EMA (European Medicines Agency)

pfizer ireland pharmaceuticals - avibactam sodium, ceftazidime pentahydrate - pneumonia, bacterial; soft tissue infections; pneumonia; urinary tract infections; gram-negative bacterial infections - antibakteriālas līdzekļi sistēmiskai lietošanai, - zavicefta is indicated in adults and paediatric patients aged 3 months and older for the treatment of the following infections:complicated intra-abdominal infection (ciai)complicated urinary tract infection (cuti), including pyelonephritishospital-acquired pneumonia (hap), including ventilator associated pneumonia (vap)treatment of patients with bacteraemia that occurs in association with, or is suspected to be associated with, any of the infections listed above. zavicefta is also indicated for the treatment of infections due to aerobic gram-negative organisms in adults and paediatric patients aged 3 months and older with limited treatment options. jāņem vērā oficiālās vadlīnijas par piemērotu izmantot antibakteriālas vielas.

الاتحاد الأوروبي - اللاتفية - 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.

لاتفيا - اللاتفية - Zāļu valsts aģentūra

angelini pharma osterreich gmbh, austria - leiprorelīna acetāts - pulveris un šķīdinātājs ilgstošas darbības injekciju suspensijas pagatavošanai - 22,5 mg

لاتفيا - اللاتفية - Zāļu valsts aģentūra

angelini pharma osterreich gmbh, austria - leiprorelīna acetāts - pulveris un šķīdinātājs ilgstošas darbības injekciju suspensijas pagatavošanai - 3,75 mg

لاتفيا - اللاتفية - Pārtikas un veterinārais dienests, Zemkopības ministrija

veyx-pharma gmbh, vācija - carbetocin - šķīdums injekcijām - 70 µg/ml - cūkas; liellopi

لاتفيا - اللاتفية - Pārtikas un veterinārais dienests, Zemkopības ministrija

"l.Ē.v." (ekstraktu rŪpnĪca), sia - šķidrums

لاتفيا - اللاتفية - Pārtikas un veterinārais dienests, Zemkopības ministrija

"l.Ē.v." (ekstraktu rŪpnĪca), sia - šķidrums