União Europeia - português - EMA (European Medicines Agency)

janssen-cilag international n.v.    - recombinant adenovirus type 26 (ad26) encoding the glycoprotein (gp) of the ebola virus zaire (zebov) mayinga strain - febre hemorrágica Ébola - vacinas - active immunization for prevention of disease caused by ebola virus (zaire ebolavirus species) in individuals ≥ 1 year of age.

União Europeia - português - EMA (European Medicines Agency)

janssen-cilag international n.v.    - recombinant modified vaccinia ankara bavarian nordic virus encoding the: ebola virus zaire (zebov) mayinga strain glycoprotein (gp); ebola virus sudan gulu strain gp; ebola virus taï forest strain nucleoprotein and the marburg virus musoke strain gp - febre hemorrágica Ébola - vacinas - active immunization for prevention of disease caused by ebola virus (zaire ebolavirus species) in individuals ≥ 1 year of age.

União Europeia - português - EMA (European Medicines Agency)

zoetis belgium - inactivated mycoplasma hyopneumoniae, strain p-5722-3, inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2a open reading frame 2 (orf2) protein, inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2b orf2 protein - imunológicos para suidae - suínos (para engorda) - active immunisation of pigs against porcine circovirus type 2 to reduce viral load in blood and lymphoid tissues, fecal shedding and the lesions in lymphoid tissues associated with pcv2 infection. protection was demonstrated against porcine circovirus types 2a, 2b and 2d. active immunisation of pigs against mycoplasma hyopneumoniae to reduce the lung lesions associated with mycoplasma hyopneumoniae infection.  onset of immunity (both vaccination schedules): 3 weeks after (the last) vaccination.  duration of immunity (both vaccination schedules): 23 weeks after (the last) vaccination.  in addition, vaccination has been shown to reduce body weight gain losses under field conditions.

União Europeia - português - EMA (European Medicines Agency)

pfizer europe ma eeig - pneumococcal polysaccharide serotype 1, pneumococcal polysaccharide serotype 3, pneumococcal polysaccharide serotype 4, pneumococcal polysaccharide serotype 5, pneumococcal polysaccharide serotype 6a, pneumococcal polysaccharide serotype 6b, pneumococcal polysaccharide serotype 7f, pneumococcal polysaccharide serotype 8, pneumococcal polysaccharide serotype 9v, pneumococcal polysaccharide serotype 10a, pneumococcal polysaccharide serotype 11a, pneumococcal polysaccharide serotype 12f, pneumococcal polysaccharide serotype 14, pneumococcal polysaccharide serotype 15b, pneumococcal polysaccharide serotype 18c, pneumococcal polysaccharide serotype 19a, pneumococcal polysaccharide serotype 19f, pneumococcal polysaccharide serotype 22f, pneumococcal polysaccharide serotype 23f, pneumococcal polysaccharide serotype 33f - infecções pneumocócicas - vacinas - 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. apexxnar should be used in accordance with official recommendations. .

União Europeia - português - EMA (European Medicines Agency)

seqirus s.r.l.  - zoonotic influenza vaccine (h5n1) (surface antigen, inactivated, adjuvanted), influenza virus surface antigens (haemagglutinin and neuraminidase) of strain: a/turkey/turkey/1/05 (h5n1)-like strain (nibrg-23) - influenza a virus, h5n1 subtype - vacinas - active immunisation against h5 subtype of influenza a virus.

Portugal - português - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

medochemie iberia, s.a. - ambroxol - solução oral - 6 mg/ml - ambroxol, cloridrato 6 mg/ml - ambroxol - genérico - duração do tratamento: curta ou média duração

Portugal - português - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

laboratórios basi - indústria farmacêutica, s.a - paracetamol - suspensão oral - 40 mg/ml - paracetamol 40 mg/ml - paracetamol - genérico - duração do tratamento: curta ou média duração

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

wyeth indÚstria farmacÊutica ltda - vacinas

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

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

Portugal - português - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

laboratório edol - produtos farmacêuticos, s.a. - ofloxacina - colírio, solução - 3 mg/ml - ofloxacina 3 mg/ml - ofloxacin - n/a - duração do tratamento: curta ou média duração