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

nuvaxovid

novavax cz, a.s. - sars cov-2 (original) recombinant spike protein, sars-cov-2 (omicron xbb.1.5) recombinant spike protein - covid-19 virus infection - covid-19 vaccines - nuvaxovid is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 12 years of age and older. het gebruik van dit vaccin moet gebeuren in overeenstemming met officiële aanbevelingen. nuvaxovid xbb. 5 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 12 years of age and older. het gebruik van dit vaccin moet gebeuren in overeenstemming met officiële aanbevelingen.

Coliprotec F4/F18 Europese Unie - Nederlands - EMA (European Medicines Agency)

coliprotec f4/f18

elanco gmbh - levende niet-pathogene escherichia coli o141: k94 (f18ac) en o8: k87 (f4ac) - immunologicals for suidae, live bacterial vaccines - varkens - voor actieve immunisatie van varkens vanaf 18 dagen tegen enterotoxigene f4-positieve en f18-positieve escherichia coli om de incidentie van matige tot ernstige post-spenen e te verminderen. coli diarree (pwd) bij geïnfecteerde varkens en om de fecale uitscheiding van enterotoxigene f4-positieve en f18-positieve e te verminderen. coli van geïnfecteerde varkens.

Bluevac BTV (previously known as Bluevac BTV8) Europese Unie - Nederlands - EMA (European Medicines Agency)

bluevac btv (previously known as bluevac btv8)

cz veterinaria s.a. - bluetongue virus vaccine serotypes 1 or 4 or 8 [inactivated] - immunologische - sheep; cattle - sheepactive vaccinatie tegen blauwtong virus serotype 8 om te voorkomen dat viraemia en het verminderen van klinische symptomen. begin immuniteit: 20 dagen na tweede dosis. duur van de immuniteit: 1 jaar na de tweede dosis. cattleactive vaccinatie tegen blauwtong virus serotype 8 om te voorkomen dat viraemia. begin immuniteit: 31 dagen na tweede dosis. duur van de immuniteit: 1 jaar na de tweede dosis.

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

bimervax

hipra human health s.l. - sars-cov-2 virus recombinant spike (s) protein receptor binding domain (rbd) fusion heterodimer – b.1.351-b.1.1.7 strains - covid-19 virus infection - vaccins - bimervax is indicated as a booster for active immunisation to prevent covid-19 in individuals 16 years of age and older who have previously received a mrna covid-19 vaccine.

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

coxevac

ceva santé animale - geïnactiveerd coxiella burnetii-vaccin, stam 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.

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

neocolipor

boehringer ingelheim vetmedica gmbh - e. coli adhesin f4 (f4ab, f4ac, f4ad), e. coli adhesin f5, e. coli adhesin f6, e. coli adhesin f41 - immunologicals for suidae, inactivated bacterial vaccines (including mycoplasma, toxoid and chlamydia) - sows; sows (nullipar) - vermindering van neonatale enterotoxicose bij biggen, veroorzaakt door e. coli-stammen, die de adhesinen f4ab, f4ac, f4ad, f5, f6 en f41 tot expressie brengen, gedurende de eerste levensdagen.

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

porcilis pcv id

intervet international b.v. - varkenscircovirus type 2 orf2 subeenheid antigeen - immunologicals for suidae, inactivated viral vaccines - varkens - for the active immunisation of pigs to reduce viraemia, virus load in lungs and lymphoid tissues and virus shedding caused by pcv2 infection.  to reduce loss of daily weight gain and mortality associated with pcv2 infection.

ProteqFlu-Te Europese Unie - Nederlands - EMA (European Medicines Agency)

proteqflu-te

boehringer ingelheim vetmedica gmbh - clostridium tetani toxoid / vcp 2242 virus / vcp1529 virus / vcp1533 virus / virus vcp3011 - immunologicals for equidae, live viral and inactivated bacterial vaccines, equine influenza virus + clostridium - paarden - actieve immunisatie van paarden van vier maanden of ouder tegen paardeninfluenza om klinische verschijnselen en virusexcretie na infectie te verminderen, en tegen tetanus om mortaliteit te voorkomen.

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.

Zulvac 1+8 Ovis Europese Unie - Nederlands - EMA (European Medicines Agency)

zulvac 1+8 ovis

zoetis belgium sa - inactivated bluetongue virus, serotype 1, strain btv-1/alg2006/01, inactivated bluetongue virus, serotype 8, strain btv-8/bel2006/02 - bluetongue virus, sheep, inactivated viral vaccines - schapen - actieve immunisatie van schapen van 1. 5 maanden oud om viremie veroorzaakt door bluetonguevirus, serotypen 1 en 8 te voorkomen. begin immuniteit: 21 dagen na voltooiing van het primaire vaccinatieschema. duur van de immuniteit: 12 maanden.