Unión Europea - español - EMA (European Medicines Agency)

intervet international bv - clostridium perfringens tipo c / escherichia coli f4ab / e. coli f4ac / e. coli f5 / e. coli f6 / lt de e. coli - inmunológicos - cerdos - para la inmunización pasiva de la progenie por activos de vacunación de las cerdas y cerdas jóvenes para reducir la mortalidad y los signos clínicos durante los primeros días de vida, causados por estas cepas de escherichia coli que expresan las adhesinas f4ab (k88ab), f4ac (k88ac), f5 (k99) o f6 (987p) y producida por el clostridium perfringens tipo c.

España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

cz vaccines s.a.u. - clostridium perfringens tipo c, toxoide beta - emulsiÓn inyectable - clostridium perfringens tipo c, toxoide beta 10ui - escherichia + clostridium - lechones; cerdas

Unión Europea - español - EMA (European Medicines Agency)

ceva santé animale - clostridium perfringens type c, beta1 toxoid / clostridium perfringens, type a, alpha toxoid / clostridium perfringens, type a, beta2 toxoid / escherichia coli, fimbrial adhesin f4ab / escherichia coli, fimbrial adhesin f4ac / escherichia coli, fimbrial adhesin f5 / escherichia coli, fimbrial adhesin f6 - immunologicals for suidae, inactivated bacterial vaccines (including mycoplasma, toxoid and chlamydia) escherichia + clostridium - cerdos - for the passive immunisation of progeny by active immunisation of pregnant sows and gilts to reduce:-           clinical signs (severe diarrhoea) and mortality caused by escherichia coli strains expressing the fimbrial adhesins f4ab, f4ac, f5 and f6-           clinical signs (diarrhoea during the first days of life) associated with clostridium perfringens type a expressing alpha and beta 2 toxins-           clinical signs and mortality associated with haemorrhagic and necrotising enteritis caused by clostridium perfringens type c expressing beta1 toxin.

Unión Europea - español - EMA (European Medicines Agency)

janssen-cilag international nv - adenovirus type 26 encoding the sars-cov-2 spike glycoprotein (ad26.cov2-s) - covid-19 virus infection - vacunas - jcovden is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 18 years of age and older. el uso de esta vacuna debe estar en conformidad con las recomendaciones oficiales.

Unión Europea - español - EMA (European Medicines Agency)

ceva santé animale - inactivated fimbrial adhesins of escherichia coli f4ab, inactivated fimbrial adhesins of escherichia coli f4ac, inactivated fimbrial adhesins of escherichia coli f5, inactivated fimbrial adhesins of escherichia coli f6 - inmunológicos para suidos - cerdos - for the passive immunisation of progeny by active immunisation of pregnant sows and gilts to reduce clinical signs (severe diarrhoea) and mortality caused by escherichia coli strains expressing the fimbrial adhesins f4ab, f4ac, f5 and f6.

Unión Europea - español - EMA (European Medicines Agency)

novartis vaccines and diagnostics s.r.l. - antígenos de superficie del virus de la gripe (hemaglutinina y neuraminidasa) de la cepa a / viet nam / 1194/2004 (h5n1) - influenza, human; immunization; disease outbreaks - vacunas - inmunización activa contra el subtipo h5n1 del virus influenza a. , , this indication is based on immunogenicity data from healthy subjects from the age of 18 years onwards following administration of two doses of the vaccine containing a/vietnam/1194/2004 (h5n1)-like strain. , , prepandemic influenza vaccine (h5n1) novartis vaccines and diagnostic should be used in accordance with official recommendations.

Unión Europea - español - 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 - vacunas - 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.

Unión Europea - español - 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 - vacunas - active immunisation against h5 subtype of influenza a virus.

Unión Europea - español - EMA (European Medicines Agency)

valneva austria gmbh - covid-19 vaccine (inactivated, adjuvanted, adsorbed) - covid-19 virus infection - vacunas - covid-19 vaccine (inactivated, adjuvanted) valneva is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 18 to 50 years of age.  the use of this vaccine should be in accordance with official recommendations.

Unión Europea - español - EMA (European Medicines Agency)

intervet international bv - clostridium-perfringens-type-a alfa toxoide - inmunológicos para aves - pollo - para la inmunización activa de pollos para proporcionar inmunización pasiva contra la enteritis necrótica a su progenie, durante el período de postura. para reducir la mortalidad y la incidencia y la gravedad de las lesiones causadas por la enteritis necrótica inducida por clostridium-perfringens-tipo-a. la eficacia se demostró mediante el desafío de los pollitos aproximadamente tres semanas después de la eclosión. el inicio de la transferencia pasiva de inmunidad: 6 semanas después de la finalización del procedimiento de vacunación. la duración de la transferencia pasiva de inmunidad: 51 semanas después de la finalización del procedimiento de vacunación.