Eiropas Savienība - latviešu - EMA (European Medicines Agency)

paion deutschland gmbh - angiotensīna ii acetāts - hypotension; shock - agents, kas iedarbojas uz renīna-angiotenzīna sistēmu - giapreza ir indicēts, lai ārstētu ugunsizturīgo hipotensija pieaugušajiem ar septisko vai citu sadales šoks, kas paliek hypotensive neskatoties uz atbilstoša apjoma atgūšanas un piemērošanu, kateholamīnu, un citus pieejamus vasopressor terapiju.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

roche registration gmbh - baloxavir marboxil - gripas, cilvēka - pretvīrusu līdzekļi sistēmiskai lietošanai - treatment of influenzaxofluza is indicated for the treatment of uncomplicated influenza in patients aged 1 year and above. post exposure prophylaxis of influenzaxofluza is indicated for post-exposure prophylaxis of influenza in individuals aged 1 year and above. xofluza should be used in accordance with official recommendations.

Latvija - latviešu - Zāļu valsts aģentūra

fresenius kabi polska sp.z o.o., poland - bendamustīna hidrohlorīds - pulveris infūziju šķīduma koncentrāta pagatavošanai - 2,5 mg/ml

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

roche registration gmbh  - risdiplam - muskuļu atrofija, mugurkaula - other drugs for disorders of the musculo-skeletal system - evrysdi is indicated for the treatment of 5q spinal muscular atrophy (sma) in patients with a clinical diagnosis of sma type 1, type 2 or type 3 or with one to four smn2 copies.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

baxalta innovations gmbh - nonakogs, gamma - hemophilia b - antihemorāģija - Ārstēšanas un profilakses asiņošanas pacientiem ar hemofilijas b (iedzimtas ix faktora deficīts).

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

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.

Latvija - latviešu - Zāļu valsts aģentūra

baxalta innovations gmbh, austria - factor viii inhibitor bypassing activity - pulveris un šķīdinātājs infūziju šķīduma pagatavošanai - 25 v/ml

Latvija - latviešu - Zāļu valsts aģentūra

baxalta innovations gmbh, austria - factor viii inhibitor bypassing activity - pulveris un šķīdinātājs infūziju šķīduma pagatavošanai - 50 v/ml

Latvija - latviešu - Zāļu valsts aģentūra

baxalta innovations gmbh, austria - factor viii inhibitor bypassing activity - pulveris un šķīdinātājs infūziju šķīduma pagatavošanai - 100 v/ml

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

roche registration gmbh - cobimetinib hemifumarāts - melanoma - antineoplastiski līdzekļi - cotellic ir indicēts lietošanai kombinācijā ar vemurafenibu pieaugušiem pacientiem ar nerezecējamu vai metastātisku melanomu ar braf v600 mutāciju.