Supemtek União Europeia - português - EMA (European Medicines Agency)

supemtek

sanofi pasteur - influenza a virus subtype h1n1 haemagglutinin, recombinant, influenza a virus subtype h3n2 haemagglutinin, recombinant, influenza b virus victoria lineage haemagglutinin, recombinant, influenza b virus yamagata lineage haemagglutinin, recombinant - influenza humana - vacinas - supemtek is indicated for active immunization for the prevention of influenza disease in adults. supemtek should be used in accordance with official recommendations.

Arexvy União Europeia - português - EMA (European Medicines Agency)

arexvy

glaxosmithkline biologicals s.a.  - respiratory syncytial virus recombinant glycoprotein f stabilised in the pre-fusion conformation (rsvpref3) produced in chinese hamster ovary (cho) cells by recombinant dna technology - infecções respiratórias do vírus sincitial - vacinas - arexvy is indicated for active immunisation for the prevention of lower respiratory tract disease (lrtd) caused by respiratory syncytial virus in adults 60 years of age and older. o uso desta vacina deve ser de acordo com as recomendações oficiais.

Vaxneuvance União Europeia - português - EMA (European Medicines Agency)

vaxneuvance

merck sharp & dohme b.v.  - pneumococcal polysaccharide conjugate vaccine (adsorbed) - infecções pneumocócicas - pneumococcus, purified polysaccharides antigen conjugated - vaxneuvance is indicated for active immunisation for the prevention of invasive disease, pneumonia and acute otitis media caused by streptococcus pneumoniae in infants, children and adolescents from 6 weeks to less than 18 years of age. vaxneuvance is indicated for active immunisation for the prevention of invasive disease and pneumonia caused by streptococcus pneumoniae in individuals 18 years of age and older. veja as seções 4. 4 e 5. 1 para informações sobre proteção contra serotipos pneumocócicos específicos. the use of vaxneuvance should be in accordance with official recommendations.

MenQuadfi União Europeia - português - EMA (European Medicines Agency)

menquadfi

sanofi pasteur - neisseria meningitidis group c polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group a polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group y polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group w-135 polysaccharide conjugated to tetanus toxoid - meningite, meningococo - vacinas - menquadfi is indicated for active immunisation of individuals from the age of 12 months and older against invasive meningococcal disease caused by neisseria meningitidis serogroups a, c, w, and y. the use of this vaccine should be in accordance with available official recommendations.

Abrysvo União Europeia - português - EMA (European Medicines Agency)

abrysvo

pfizer europe ma eeig - respiratory syncytial virus, subgroup a, stabilized prefusion f protein / respiratory syncytial virus, subgroup b, stabilized prefusion f protein - infecções respiratórias do vírus sincitial - vacinas - abrysvo is indicated for:passive protection against lower respiratory tract disease caused by respiratory syncytial virus (rsv) in infants from birth through 6 months of age following maternal immunisation during pregnancy. veja as seções 4. 2 e 5. active immunisation of individuals 60 years of age and older for the prevention of lower respiratory tract disease caused by rsv. o uso desta vacina deve ser de acordo com as recomendações oficiais.

Pandemrix União Europeia - português - EMA (European Medicines Agency)

pandemrix

glaxosmithkline biologicals s.a. - vírus inchavel da gripe inativado, contendo antigénio equivalente a a / california / 07/2009 (h1n1) - cepa usada usada nymc x-179a - influenza, human; immunization; disease outbreaks - vacinas contra a gripe - profilaxia da gripe causada pelo vírus a (h1n1) v 2009. a pandemrix só deve ser utilizada se as vacinas vacinais estacionais trivalentes / quadrivalentes recomendadas não estiverem disponíveis e se a imunização contra (h1n1) v for considerada necessária (ver seções 4. 4 e 4. pandemrix deve ser usado de acordo com orientação oficial.

PREVENAR 13 Brasil - português - ANVISA (Agência Nacional de Vigilância Sanitária)

prevenar 13

pfizer brasil ltda - polissacarÍdeo capsular de streptococcus pneumoniae sorotipo 1, polissacarÍdeo capsular de streptococcus pneumoniae sorotipo 6b, polissacarÍdeo capsular de streptococcus pneumoniae sorotipo 3 , polissacarÍdeo capsular de streptococcus pneumoniae sorotipo 4 , polissacarÍdeo capsular de streptococcus pneumoniae sorotipo 5, polissacarÍdeo capsular de streptococcus pneumoniae sorotipo 6a , polissacarÍdeo capsular de streptococcus pneumoniae sorotipo 7f , polissacarÍdeo capsular de streptococcus pneumoniae sorot - vacinas

Dengvaxia União Europeia - português - EMA (European Medicines Agency)

dengvaxia

sanofi pasteur - chimeric yellow fever dengue virus serotype 1 (live, attenuated), chimeric yellow fever dengue virus serotype 2 (live, attenuated), chimeric yellow fever dengue virus serotype 3 (live, attenuated), chimeric yellow fever dengue virus serotype 4 (live, attenuated) - a dengue - vacinas - dengvaxia is indicated for the prevention of dengue disease caused by dengue virus serotypes 1, 2, 3 and 4 in individuals 6 to 45 years of age with test-confirmed previous dengue infection (see sections 4. 2, 4. 4 e 4. o uso de dengvaxia deve estar em conformidade com as recomendações oficiais.

Flublok Quadrivalente Brasil - português - ANVISA (Agência Nacional de Vigilância Sanitária)

flublok quadrivalente

biolab sanus farmacÊutica ltda - cepa influenza tipo b, cepa influenza tipo a (h1n1), cepa influenza tipo a (h3n2) - vacinas

Flublok Quadrivalente Brasil - português - ANVISA (Agência Nacional de Vigilância Sanitária)

flublok quadrivalente

sanofi medley farmacÊutica ltda. - cepa influenza tipo a (h1n1), cepa influenza tipo a (h3n2), cepa influenza tipo b - vacinas