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

zoetis spain, s.l. - mycoplasma gallisepticum inactivado cepa r-980 - emulsiÓn inyectable - excipientes: parafina liquida ligera, sorbitan sesquioleato, polisorbato 80 - micoplasma - gallinas ponedoras, pavas, pollos reproductores

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

pfizer, s.l. - mycoplasma gallisepticum inactivado cepa r-980 - emulsiÓn inyectable - excipientes: formalina, aceite mineral blanco, sorbitan sesquioleato, tween 80 - micoplasma - gallinas ponedoras, pavos, pollos reproductores

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

cz vaccines s.a.u. - mycoplasma agalactiae, inactivado, cepa n-262 - emulsiÓn inyectable - mycoplasma agalactiae, inactivado, cepa n-262 137 - vacunas bacterianas inactivadas (incluyendo micoplasma, clamidia y toxoide) - ovino; caprino

Unión Europea - español - EMA (European Medicines Agency)

zoetis belgium sa - inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2 orf2 protein, inactivated mycoplasma hyopneumoniae, strain p-5722-3 - inactivado virales y bacterianas inactivadas vacunas - cerdos - para la inmunización activa de cerdos desde las 3 semanas de edad contra el circovirus porcino tipo 2 (pcv2) para reducir la carga viral en sangre y tejidos linfoides y la excreción fecal causada por la infección con pcv2. para la inmunización activa de cerdos mayores de 3 semanas contra mycoplasma hyopneumoniae para reducir las lesiones pulmonares causadas por la infección con m. hyopneumoniae.

Unión Europea - español - EMA (European Medicines Agency)

laboratorios hipra, s.a. - mycoplasma hyopneumoniae, strain 7304 (nexhyon), expressing the capsid protein of porcine circovirus type 2a, inactivated - immunologicals for suidae, inactivated viral and inactivated bacterial vaccines - cerdos - for the active immunisation of pigs:to reduce lung lesions associated with porcine enzootic pneumonia caused by mycoplasma hyopneumoniae. also, to reduce the incidence of these lesions (as observed in field studies). to reduce viraemia, virus load in lungs and lymphoid tissues and the duration of the viraemic period associated with diseases caused by porcine circovirus type 2 (pcv2). efficacy against pcv2 genotypes a, b and d has been demonstrated in field studies. to reduce culling rate and the loss of daily weight gain caused by mycoplasma hyopneumoniae and/or pcv2 related diseases (as observed at 6 months of age in field studies). mycoplasma hyopneumoniae: onset of immunity: 3 weeks after vaccinationduration of immunity: 23 weeks after vaccinationporcine circovirus type 2:onset of immunity: 2 weeks after vaccinationduration of immunity: 22 weeks after vaccinationin addition, a reduction in nasal and faecal shedding and the duration of nasal excretion of pcv2 was demonstrated in animals challenged at 4 weeks and at 22 weeks after vaccination.

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 b.v. - circovirus porcino tipo 2 (pcv2) orf2 de la subunidad de antígeno, mycoplasma hyopneumoniae j cepa inactivada - immunologicals for suidae, inactivated viral and inactivated bacterial vaccines - los cerdos (de engorde) - para la inmunización activa de cerdos para reducir viraemia, la carga del virus en los pulmones y los tejidos linfoides, de la eliminación del virus causado por circovirus porcino tipo 2 (pcv2), la infección y la gravedad de las lesiones pulmonares causadas por la infección por mycoplasma hyopneumoniae. para reducir la pérdida de ganancia diaria de peso durante el período de finalización frente a infecciones con mycoplasma hyopneumoniae y / o pcv2 (como se observó en estudios de campo).

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)

ceva santé animale - vacuna inactivada de coxiella burnetii, cepa nine mile - immunologicals for bovidae, inactivated bacterial vaccines (including mycoplasma, toxoid and chlamydia) - goats; cattle - cattle: , for the active immunisation of cattle to lower the risk for non-infected animals vaccinated when non-pregnant to become shedder (5 times lower probability in comparison with animals receiving a placebo), and to reduce shedding of coxiella burnetii in these animals via milk and vaginal mucus. , onset of immunity: not established. , duration of immunity: 280 days after completion of the primary vaccination course. , goats: , for the active immunisation of goats to reduce abortion caused by coxiella burnetii and to reduce shedding of the organism via milk, vaginal mucus, faeces and placenta. , onset of immunity: not established. , duration of immunity: one year after completion of the primary vaccination course.

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.