Comirnaty Euroopa Liit - eesti - 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 - vaktsiinid - 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. kasutamist see vaktsiin peaks olema kooskõlas ametlike soovitustega.

POTASSIUM CHLORIDE/GLUCOSE FRESENIUS 1,5 MG/50 MG/ML infusioonilahus Eesti - eesti - Ravimiamet

potassium chloride/glucose fresenius 1,5 mg/50 mg/ml infusioonilahus

fresenius kabi deutschland gmbh - kaaliumkloriid+glükoos - infusioonilahus - 1,5mg+50mg 1ml 1000ml 10tk

POTASSIUM CHLORIDE/GLUCOSE FRESENIUS 3 MG/50 MG/ML infusioonilahus Eesti - eesti - Ravimiamet

potassium chloride/glucose fresenius 3 mg/50 mg/ml infusioonilahus

fresenius kabi deutschland gmbh - kaaliumkloriid+glükoos - infusioonilahus - 3mg+50mg 1ml 500ml 10tk; 3mg+50mg 1ml 1000ml 10tk

Prevenar Euroopa Liit - eesti - EMA (European Medicines Agency)

prevenar

pfizer limited - pneumococcal oligosaccharide serotype 18c, pneumococcal polysaccharide serotype 19f, pneumococcal polysaccharide serotype 23f, pneumococcal polysaccharide serotype 4, pneumococcal polysaccharide serotype 6b, pneumococcal polysaccharide serotype 9v, pneumococcal polysaccharide serotype 14 - pneumococcal infections; immunization - vaktsiinid - haiguste põhjustatud streptococcus pneumoniaeserotüüpide 4, 6b, 9v, 14, 18 c, 19f ja 23f (sealhulgas sepsis, meningiit, pneumoonia, baktereemia ja äge keskkõrvapõletik) imikutel ja lastel kaks kuud kuni viieaastase. kasutada prevenar tuleks kindlaks määrata, lähtudes ametlikest soovitustest, võttes arvesse mõju invasiivse haiguse erinevates vanuserühmades samuti muutlikkust ja serotüübi epidemioloogiat erinevates geograafilistes piirkondades.

BOSENTAN ACCORD õhukese polümeerikattega tablett Eesti - eesti - Ravimiamet

bosentan accord õhukese polümeerikattega tablett

accord healthcare b.v. - bosentaan - õhukese polümeerikattega tablett - 125mg 120tk; 125mg 112tk; 125mg 56tk

BETAHISTINE ACCORD tablett Eesti - eesti - Ravimiamet

betahistine accord tablett

accord healthcare b.v. - beetahistiin - tablett - 24mg 90tk; 24mg 20tk; 24mg 60tk; 24mg 84tk; 24mg 50tk; 24mg 100tk

BOSENTAN ACCORD õhukese polümeerikattega tablett Eesti - eesti - Ravimiamet

bosentan accord õhukese polümeerikattega tablett

accord healthcare b.v. - bosentaan - õhukese polümeerikattega tablett - 62,5mg 56tk; 62,5mg 14tk; 62,5mg 112tk

FULVESTRANT ACCORD süstelahus süstlis Eesti - eesti - Ravimiamet

fulvestrant accord süstelahus süstlis

accord healthcare b.v. - fulvestrant - süstelahus süstlis - 250mg 5ml 5ml 2tk

LORATADINE ACCORD tablett Eesti - eesti - Ravimiamet

loratadine accord tablett

accord healthcare b.v. - loratadiin - tablett - 10mg 28tk; 10mg 7tk; 10mg 100tk; 10mg 60tk; 10mg 10tk; 10mg 50tk; 10mg 14tk; 10mg 30tk