Hiprabovis IBR Marker Live Europese Unie - Nederlands - EMA (European Medicines Agency)

hiprabovis ibr marker live

laboratorios hipra s.a - levend ge-tk- dubbel-gen-verwijderd runder herpes-virus type 1, stam ceddel: 106,3-107,3 ​​ccid50 - immunologische - vee - voor de actieve immunisatie van runderen vanaf drie maanden tegen runderherpesvirus type 1 (bohv-1) om de klinische symptomen van infectieuze boviene rhinotracheïtis (ibr) en veldvirusuitscheiding te verminderen. begin immuniteit: 21 dagen na voltooiing van het basisvaccinatieschema. duur van de immuniteit: 6 maanden na voltooiing van het basisvaccinatieschema.

Innovax-ND-ILT Europese Unie - Nederlands - EMA (European Medicines Agency)

innovax-nd-ilt

intervet international b.v. - cell-associated live recombinant turkey herpesvirus (strain hvt/ndv/ilt) expressing the fusion protein of newcastle disease virus and the glycoproteins gd and gi of infectious laryngotracheitis virus - immunologicals voor aves - embryonated chicken eggs; chicken - for active immunisation of one-day-old chicks or embryonated chicken eggs:to reduce mortality and clinical signs caused by newcastle disease (nd) virus,to reduce mortality, clinical signs and lesions caused by avian infectious laryngotracheitis (ilt) virus and marek’s disease (md) virus.

Dengvaxia Europese Unie - Nederlands - 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) - dengue - vaccins - 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 en 4. het gebruik van dengvaxia moet gebeuren in overeenstemming met officiële aanbevelingen.

Qdenga Europese Unie - Nederlands - EMA (European Medicines Agency)

qdenga

takeda gmbh - dengue virus, serotype 2, expressing dengue virus, serotype 1, surface proteins, live, attenuated, dengue virus, serotype 2, expressing dengue virus, serotype 3, surface proteins, live, attenuated, dengue virus, serotype 2, expressing dengue virus, serotype 4, surface proteins, live, attenuated, dengue virus, serotype 2, live, attenuated - dengue - vaccins - qdenga is indicated for the prevention of dengue disease in individuals from 4 years of age. the use of qdenga should be in accordance with official recommendations.

Innovax-ILT Europese Unie - Nederlands - EMA (European Medicines Agency)

innovax-ilt

intervet international b.v. - celgebonden levend recombinant kalkoenherpesvirus (stam hvt / ilt-138), dat de glycoproteïnen gd en gi van infectieus laryngotracheïtisvirus tot expressie brengt - immunologicals voor aves, levende virale vaccins - kip - voor actieve immunisatie van kuikens van één dag om mortaliteit, klinische symptomen en laesies als gevolg van infectie met aviaire infectieuze laryngotracheïtis (ilt) -virus en het marek-virus (md) -virus te verminderen.

Ultifend ND IBD Europese Unie - Nederlands - EMA (European Medicines Agency)

ultifend nd ibd

ceva-phylaxia veterinary biologicals co. ltd - turkey herpes virus, strain rhvt/nd/ibd, expressing the fusion protein of newcastle disease virus and the vp2 protein of infectious bursal disease virus, live recombinant - immunologicals voor aves - embryonated chicken eggs; chicken - for the active immunisation of one-day-old chicks or 18-day-old chicken embryonated eggs to reduce mortality, clinical signs and lesions caused by newcastle disease virus (ndv) and to reduce virus shedding; to reduce mortality, clinical signs and bursa lesions caused by very virulent infectious bursal disease virus (ibdv); to reduce mortality, clinical signs and lesions caused by classical marek’s disease virus (mdv).

Vectormune ND Europese Unie - Nederlands - EMA (European Medicines Agency)

vectormune nd

ceva-phylaxia co. ltd. - met cellen geassocieerd levend recombinant kalkoenherpesvirus (rhvt / nd) dat het fusie-eiwit van de d-26-lentogene stam van newcastle-diseases-virus tot expressie brengt - immunologicals voor aves, levende virale vaccins - chicken; embryonated eggs - voor de actieve immunisatie van 18 dagen oude embryonale kip eieren of de eendagskuikens aan het verminderen van de mortaliteit en de klinische symptomen veroorzaakt door de ziekte van newcastle-virus en het verminderen van de sterfte, klinische symptomen en letsels veroorzaakt door marek ' s disease virus met een fenotype "virulente".

Poulvac Marek H.V.T inj. susp. (lyof.) i.m./s.c. flac. België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

poulvac marek h.v.t inj. susp. (lyof.) i.m./s.c. flac.

zoetis belgium - levend kalkoenherpesvirus, stam fc126 =10exp3,0 pfu/do - lyofilisaat voor suspensie voor injectie - levend kalkoenherpesvirus, stam fc126 - avian herpes virus (marek's disease) - pluimvee

Mhyosphere PCV ID Europese Unie - Nederlands - EMA (European Medicines Agency)

mhyosphere pcv id

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 - varkens - 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.

Suvaxyn CSF Marker Europese Unie - Nederlands - EMA (European Medicines Agency)

suvaxyn csf marker

zoetis belgium sa - live recombinant e2 gene-deleted bovine viral diarrhoea virus containing classical swine fever virus e2 gene (cp7_e2alf) - live viral vaccines, immunologicals for suidae - varkens - voor actieve immunisatie van varkens vanaf de leeftijd van 7 weken om sterfte te voorkomen en infectie en ziekten veroorzaakt door het klassieke varkenspestvirus (csfv) te verminderen. onset of immunity: 14 days after vaccinationduration of immunity: at least 6 months after vaccinationfor active immunisation of breeding females to reduce transplacental infection caused by csfv. onset of immunity: 21 days after vaccinationduration of immunity has not been demonstrated.