Oxaliplatin Actavis 5 mg/ml koncentrāts infūziju šķīduma pagatavošanai Latvija - latviešu - Zāļu valsts aģentūra

oxaliplatin actavis 5 mg/ml koncentrāts infūziju šķīduma pagatavošanai

actavis group ptc ehf., iceland - oksaliplatīns - koncentrāts infūziju šķīduma pagatavošanai - 5 mg/ml

Atipam Latvija - latviešu - Pārtikas un veterinārais dienests, Zemkopības ministrija

atipam

eurovet animal health b.v., nīderlande - atipamezols hidrohlorīds - šķīdums injekcijām - 5 mg/ml - kaķi; suņi

Nobivac Puppy DP liofilizāts un šķīdinātājs šķīduma injekcijām pagatavošanai Latvija - latviešu - Pārtikas un veterinārais dienests, Zemkopības ministrija

nobivac puppy dp liofilizāts un šķīdinātājs šķīduma injekcijām pagatavošanai

intervet international b.v., nīderlande - dzīvo suņu distemper vīrusu (cdv) celmu onderstepoort, dzīvot suņu parvovīrusa (cpv), celmu 154 - liofilizāts un šķīdinātājs šķīduma injekcijām pagatavošanai - suņi

Ubroseal Dry Cow Latvija - latviešu - Pārtikas un veterinārais dienests, Zemkopības ministrija

ubroseal dry cow

univet ltd., Īrija - bismuta bāziskais nitrāts - suspensija ievadīšanai tesmenī - 2,6 g - liellopi

Oxaliplatin-Teva 5 mg/ml koncentrāts infūziju šķīduma pagatavošanai Latvija - latviešu - Zāļu valsts aģentūra

oxaliplatin-teva 5 mg/ml koncentrāts infūziju šķīduma pagatavošanai

teva b.v., netherlands - oksaliplatīns - koncentrāts infūziju šķīduma pagatavošanai - 5 mg/ml

Vinorelbine Actavis 10 mg/ml koncentrāts infūziju šķīduma pagatavošanai Latvija - latviešu - Zāļu valsts aģentūra

vinorelbine actavis 10 mg/ml koncentrāts infūziju šķīduma pagatavošanai

actavis group ptc ehf., iceland - vinorelbīns - koncentrāts infūziju šķīduma pagatavošanai - 10 mg/ml

Oxaliplatin Hospira 5 mg/ml koncentrāts infūziju šķīduma pagatavošanai Latvija - latviešu - Zāļu valsts aģentūra

oxaliplatin hospira 5 mg/ml koncentrāts infūziju šķīduma pagatavošanai

hospira uk limited, united kingdom - oksaliplatīns - koncentrāts infūziju šķīduma pagatavošanai - 5 mg/ml

Voriconazole Sciecure 200 mg pulveris infūziju šķīduma pagatavošanai Latvija - latviešu - Zāļu valsts aģentūra

voriconazole sciecure 200 mg pulveris infūziju šķīduma pagatavošanai

sciecure pharma ltd, united kingdom - vorikonazols - pulveris infūziju šķīduma pagatavošanai - 200 mg

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

comirnaty

biontech manufacturing gmbh - single-stranded, 5’-capped messenger rna 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 - comirnaty 30 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty original/omicron ba. 1 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older who have previously received at least a primary vaccination course against covid-19. comirnaty original/omicron ba. 4-5 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty original/omicron ba. 4-5 (1. 5/1. 5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty omicron xbb. 5 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty omicron xbb. 5 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 10 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years. izmantojot šo vakcīnu, kas būtu saskaņā ar oficiālās rekomendācijas.

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

jemperli

glaxosmithkline (ireland) limited - dostarlimab - endometrial neoplasms - antineoplastic agents and antibody drug conjugates - jemparli is indicated as monotherapy for the treatment of adult patients with mismatch repair deficient (dmmr)/microsatellite instability-high (msi h) recurrent or advanced endometrial cancer (ec) that has progressed on or following prior treatment with a platinum-containing regimen.