Česká republika -
čeština -
SUKL (Státní ústav pro kontrolu léčiv)
braltus 10mcg/dáv prášek k inhalaci v tvrdé tobolce
teva pharmaceuticals cr, s.r.o., praha array - 12392 tiotropium-bromid - prášek k inhalaci v tvrdé tobolce - 10mcg/dÁv - tiotropium-bromid
Česká republika -
čeština -
SUKL (Státní ústav pro kontrolu léčiv)
tamsulosin hcl sandoz 0,4mg tvrdá tobolka s řízeným uvolňováním
sandoz gmbh, kundl array - 14672 tamsulosin-hydrochlorid - tvrdá tobolka s řízeným uvolňováním - 0,4mg - tamsulosin
Česká republika -
čeština -
SUKL (Státní ústav pro kontrolu léčiv)
methoxsalen maco pharma 20mcg/ml roztok pro úpravu krevní frakce
maco pharma, mouvaux array - 1787 methoxsalen - roztok pro úpravu krevní frakce - 20mcg/ml - jinÁ imunostimulancia
Česká republika -
čeština -
SUKL (Státní ústav pro kontrolu léčiv)
symbicort turbuhaler 320mcg/9mcg prášek k inhalaci
astrazeneca ab, södertälje array - 5362 budesonid; 14188 dihydrÁt formoterol-fumarÁtu - prášek k inhalaci - 320mcg/9mcg - formoterol a budesonid
Evropská unie -
čeština -
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 - vakcíny - 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. použití této vakcíny musí být v souladu s oficiálními doporučeními.
Česká republika -
čeština -
SUKL (Státní ústav pro kontrolu léčiv)
selenase injekČní roztok 500 mcg 50mcg/ml injekční roztok
biosyn arzneimittel gmbh, fellbach array - 5637 pentahydrÁt seleniČitanu sodnÉho - injekční roztok - 50mcg/ml - seleniČitan sodnÝ
Česká republika -
čeština -
SUKL (Státní ústav pro kontrolu léčiv)
soprobec 100mcg/dáv roztok k inhalaci v tlakovém obalu
glenmark pharmaceuticals s.r.o., praha array - 2055 beklometason-dipropionÁt - roztok k inhalaci v tlakovém obalu - 100mcg/dÁv - beklometason