Kovaltry Европска Унија - Чешки - EMA (European Medicines Agency)

kovaltry

bayer ag - octocog alfa - hemofilie a - antihemoragika - léčba a profylaxe krvácení u pacientů s hemofilií a (vrozený nedostatek faktoru viii). kovaltry lze použít pro všechny věkové skupiny.

Comirnaty Европска Унија - Чешки - 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.

Qdenga Европска Унија - Чешки - EMA (European Medicines Agency)

qdenga

takeda gmbh - dengue virus, serotype 2, expressing dengue virus, serotype 1, surface proteins, live, attenuated, dengue virus, serotype 2, expressing dengue virus, serotype 3, surface proteins, live, attenuated, dengue virus, serotype 2, expressing dengue virus, serotype 4, surface proteins, live, attenuated, dengue virus, serotype 2, live, attenuated - dengue - vakcíny - qdenga is indicated for the prevention of dengue disease in individuals from 4 years of age. the use of qdenga should be in accordance with official recommendations.

ACTAIR 100IR Sublingvální tableta Чешка - Чешки - SUKL (Státní ústav pro kontrolu léčiv)

actair 100ir sublingvální tableta

stallergenes, antony array - 2217 alergenovÝ extrakt z dermatophagoides pteronyssinus; 20601 alergenovÝ extrakt z dermatophagoides farinae - sublingvální tableta - 100ir - domÁcÍ prach, roztoČi

ACTAIR 100IR+300IR Sublingvální tableta Чешка - Чешки - SUKL (Státní ústav pro kontrolu léčiv)

actair 100ir+300ir sublingvální tableta

stallergenes, antony array - 2217 alergenovÝ extrakt z dermatophagoides pteronyssinus; 20601 alergenovÝ extrakt z dermatophagoides farinae; 2217 alergenovÝ extrakt z dermatophagoides pteronyssinus; 20601 alergenovÝ extrakt z dermatophagoides farinae - sublingvální tableta - 100ir+300ir - domÁcÍ prach, roztoČi

ACTAIR 300IR Sublingvální tableta Чешка - Чешки - SUKL (Státní ústav pro kontrolu léčiv)

actair 300ir sublingvální tableta

stallergenes, antony array - 2217 alergenovÝ extrakt z dermatophagoides pteronyssinus; 20601 alergenovÝ extrakt z dermatophagoides farinae - sublingvální tableta - 300ir - domÁcÍ prach, roztoČi

BERIATE 1000IU Prášek a rozpouštědlo pro injekční/infuzní roztok Чешка - Чешки - SUKL (Státní ústav pro kontrolu léčiv)

beriate 1000iu prášek a rozpouštědlo pro injekční/infuzní roztok

csl behring gmbh, marburg array - 3531 lidskÝ koagulaČnÍ faktor viii - prášek a rozpouštědlo pro injekční/infuzní roztok - 1000iu - koagulaČnÍ faktor viii

BERIATE 2000IU Prášek a rozpouštědlo pro injekční/infuzní roztok Чешка - Чешки - SUKL (Státní ústav pro kontrolu léčiv)

beriate 2000iu prášek a rozpouštědlo pro injekční/infuzní roztok

csl behring gmbh, marburg array - 3531 lidskÝ koagulaČnÍ faktor viii - prášek a rozpouštědlo pro injekční/infuzní roztok - 2000iu - koagulaČnÍ faktor viii

OCTAPLAS LG 45-70MG/ML Prášek a rozpouštědlo pro infuzní roztok Чешка - Чешки - SUKL (Státní ústav pro kontrolu léčiv)

octaplas lg 45-70mg/ml prášek a rozpouštědlo pro infuzní roztok

octapharma (ip) sprl, brusel array - 16576 lidskÝ plazmatickÝ protein - prášek a rozpouštědlo pro infuzní roztok - 45-70mg/ml - krevnÍ derivÁty, frakce plazmatickÝch bÍlkovin, nÁhrady plazmy

OCTAPLAS LG 45-70MG/ML Infuzní roztok Чешка - Чешки - SUKL (Státní ústav pro kontrolu léčiv)

octaplas lg 45-70mg/ml infuzní roztok

octapharma (ip) sprl, brusel array - 16576 lidskÝ plazmatickÝ protein - infuzní roztok - 45-70mg/ml - jinÉ frakce plazmatickÝch bÍlkovin