Unione Europea - italiano - EMA (European Medicines Agency)

moderna biotech spain, s.l. - single-stranded, 5’-capped messenger rna (mrna) 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 - vaccini - spikevax is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older. spikevax bivalent original/omicron ba. 1 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 years of age and older who have previously received at least a primary vaccination course against covid-19. spikevax bivalent original/omicron ba. 4-5 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older.  spikevax xbb. 5 is indicated for active immunisation to prevent covid 19 caused by sars-cov-2 in individuals 6 months of age and older. the use of this vaccine should be in accordance with official recommendations.

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

pfizer ag - tozinameranum, riltozinameranum - comirnaty® original/omicron ba.1 15/15 µg pro dosis gebrauchsfertige injektionsdispersion für personen ab 18 jahren - suspension: tozinameranum 15 µg pro dosi, riltozinameranum 15 µg pro dosi, ((4-hydroxybutyl)azanediyl)bis(hexane-6,1-diylis)bis(2-hexyldecanoas), 2-(polyethylenglycoli 2000)-n,n-ditetradecylacetamidum, 1,2-distearoyl-sn-glycero-3-phosphocholinum, cholesterolum, saccharum, trometamolum, trometamoli hydrochloridum, aqua ad iniectabile, pro dosi. - comirnaty original/omicron ba.1 15/15 µg pro dosis gebrauchsfertige injektionsdispersion ist indiziert für die aktive immunisierung zur vorbeugung der durch das sars-cov-2-virus hervorgerufenen covid-19-erkrankung bei personen ab 18 jahren - vaccini

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

glaxosmithkline vaccines s.r.l. - vaccino tetanico adsorbito - vaccino tetanico adsorbito

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

glaxosmithkline vaccines s.r.l. - vaccino poliomielitico orale, trivalente, vivo attenuato - vaccino poliomielitico orale, trivalente, vivo attenuato

Unione Europea - italiano - EMA (European Medicines Agency)

ceva santé animale - virus vaccino vivo attenuato della rabbia, ceppo spbn gasgas - prodotti immunologici per canidae, live virali vaccini - red foxes (vulpes vulpes); raccoon dogs (nyctereutes procyonoides) - per l'immunizzazione attiva di volpi e cani procione contro la rabbia per prevenire infezioni e mortalità.

Unione Europea - italiano - EMA (European Medicines Agency)

sanofi pasteur s.a. - split virus dell'influenza, inattivato, contenente l'antigene*: a/california/7/2009 (h1n1)v ceppo (x-179a)*propagato in uova. - influenza, human; immunization; disease outbreaks - vaccini - profilassi dell'influenza in una situazione pandemica ufficialmente dichiarata. vaccino contro l'influenza pandemica dovrebbe essere usato in conformità con le linee guida ufficiali.

Unione Europea - italiano - EMA (European Medicines Agency)

intervet international bv - vaccino contro il virus della febbre catarrale, sierotipo 8 (inattivato) - inattivato virali vaccini, virus della febbre catarrale degli ovini, pecore - sheep; cattle - cattle to stimulate active immunity in sheep from 6 weeks of age against bluetongue virus serotype 8 to reduce viraemia sheep to stimulate active immunity in sheep from 1 month of age against bluetongue virus serotype 8 to prevent viraemia,.

Unione Europea - italiano - EMA (European Medicines Agency)

ology bioservices ireland ltd - virus dell'influenza (intero virione, inattivato), contenente antigene di: a / vietnam / 1203/2004 (h5n1) - influenza, human; immunization; disease outbreaks - vaccini contro l'influenza - immunizzazione attiva contro il sottotipo h5n1 del virus dell'influenza a.. questa indicazione si basa sui dati di immunogenicità da soggetti dall'età di 6 mesi in poi, a seguito di somministrazione di due dosi di vaccino preparato con sottotipo h5n1 ceppi. vepacel dovrebbe essere usato in conformità con le linee guida ufficiali.

Unione Europea - italiano - EMA (European Medicines Agency)

glaxosmithkline biologicals s.a. - a / indonesia / 05/2005 (h5n1) come ceppo utilizzato (pr8-ibcdc-rg2) - influenza, human; immunization; disease outbreaks - vaccini - immunizzazione attiva contro il sottotipo h5n1 del virus dell'influenza-a. questa indicazione si basa sui dati di immunogenicità di soggetti sani a partire dall'età di 18 anni in poi, a seguito di somministrazione di due dosi di vaccino preparato con sottotipo h5n1 ceppi. prepandrix dovrebbe essere usato in conformità con le linee guida ufficiali.

Unione Europea - italiano - 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 - vaccini - 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. l'uso di questo vaccino dovrebbe essere in conformità con le raccomandazioni ufficiali.