Kesimpta 欧盟 - 拉脱维亚文 - EMA (European Medicines Agency)

kesimpta

novartis ireland ltd - ofatumumabs - multiplā skleroze, recidivējoši-pārskaitot - immunosuppressant - kesimpta is indicated for the treatment of adult patients with relapsing forms of multiple sclerosis (rms) with active disease defined by clinical or imaging features (see section 5.

Sunlenca 欧盟 - 拉脱维亚文 - EMA (European Medicines Agency)

sunlenca

gilead sciences ireland unlimited company - lenacapavir sodium - hiv infekcijas - pretvīrusu līdzekļi sistēmiskai lietošanai - sunlenca injection, in combination with other antiretroviral(s), is indicated for the treatment of adults with multidrug resistant hiv 1 infection for whom it is otherwise not possible to construct a suppressive anti viral regimen (see sections 4. 2 un 5. sunlenca tablet, in combination with other antiretroviral(s), is indicated for the treatment of adults with multidrug resistant hiv 1 infection for whom it is otherwise not possible to construct a suppressive anti viral regimen, for oral loading prior to administration of long-acting lenacapavir injection (see sections 4. 2 un 5.

Esmocard Lyo 2500 mg pulveris infūziju šķīduma koncentrāta pagatavošanai 拉脱维亚 - 拉脱维亚文 - Zāļu valsts aģentūra

esmocard lyo 2500 mg pulveris infūziju šķīduma koncentrāta pagatavošanai

orpha-devel handels und vertriebs gmbh, austria - esmolola hidrohlorīds - pulveris infūziju šķīduma koncentrāta pagatavošanai - 2500 mg

Sinora 1 mg/ml koncentrāts infūziju šķīduma pagatavošanai 拉脱维亚 - 拉脱维亚文 - Zāļu valsts aģentūra

sinora 1 mg/ml koncentrāts infūziju šķīduma pagatavošanai

sintetica gmbh, germany - norepinefrīns - koncentrāts infūziju šķīduma pagatavošanai - 1 mg/ml

Comirnaty 欧盟 - 拉脱维亚文 - 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.

Paliperidone Teva 75 mg ilgstošās darbības suspensija injekcijām 拉脱维亚 - 拉脱维亚文 - Zāļu valsts aģentūra

paliperidone teva 75 mg ilgstošās darbības suspensija injekcijām

teva gmbh, germany - paliperidons - ilgstošās darbības suspensija injekcijām - 75 mg

Paliperidone Teva 100 mg ilgstošās darbības suspensija injekcijām 拉脱维亚 - 拉脱维亚文 - Zāļu valsts aģentūra

paliperidone teva 100 mg ilgstošās darbības suspensija injekcijām

teva gmbh, germany - paliperidons - ilgstošās darbības suspensija injekcijām - 100 mg

Paliperidone Teva 150 mg ilgstošās darbības suspensija injekcijām 拉脱维亚 - 拉脱维亚文 - Zāļu valsts aģentūra

paliperidone teva 150 mg ilgstošās darbības suspensija injekcijām

teva gmbh, germany - paliperidons - ilgstošās darbības suspensija injekcijām - 150 mg

Wakix 欧盟 - 拉脱维亚文 - EMA (European Medicines Agency)

wakix

bioprojet pharma - pitolisant - narkolepsija - other nervous system drugs - wakix is indicated in adults, adolescents and children from the age of 6 years for the treatment of narcolepsy with or without cataplexy (see also section 5.

Geloplasma šķīdums infūzijām 拉脱维亚 - 拉脱维亚文 - Zāļu valsts aģentūra

geloplasma šķīdums infūzijām

fresenius kabi polska sp.z o.o., poland - Želatīns, natrii chloridum, magnija chloridum hexahydricum, kalii chloridum, natrii lactatis risinājums - Šķīdums infūzijām