Unia Europejska - słowacki - EMA (European Medicines Agency)

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 - imunologická liečba - 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).

Unia Europejska - słowacki - 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 - ošípané - 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.

Unia Europejska - słowacki - EMA (European Medicines Agency)

intervet international b.v. - live myxoma vectored rhd vírus kmeň 009, live myxoma vectored rhd vírus kmeň mk1899 - immunologicals pre leporidae - králiky - pre aktívnej imunizácie králikov z 5 týždňov veku a ďalej na zníženie úmrtnosti a klinické príznaky myxomatosis a králik hemoragickú ochorenia (rhd) spôsobené klasická rhd vírus (rhdv1) a rhd typ 2 vírus (rhdv2).

Unia Europejska - słowacki - EMA (European Medicines Agency)

intervet international bv - live myxoma-vectored králik-hemoragickú-ochorenia vírus kmeň 009 - imunologické - králiky - na aktívnu imunizáciu králikov od veku piatich týždňov na zníženie úmrtnosti a klinických príznakov myxomatózy a na prevenciu úmrtnosti v dôsledku hemoragickej choroby králikov. nástup imunity: 3 týždne. trvanie imunity: 1 rok.

Unia Europejska - słowacki - EMA (European Medicines Agency)

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 - ošípané - pre aktívnej imunizácie ošípaných od 7 týždňov veku a ďalej, aby sa zabránilo úmrtnosti a zníženie infekcie a ochorenia spôsobené classical swine fever virus (csfv). 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.

Unia Europejska - słowacki - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains), attenuated feline panleucopenia virus (pli iv), felv recombinant canarypox virus (vcp97) - immunologicals pre felidae, - mačky - active immunisation of cats aged 8 weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs ;against feline panleucopenia to prevent mortality and clinical signs;against leukaemia to prevent persistent viraemia and clinical signs of the related disease. onsets of immunity are 1 week after primary vaccination course for rhinotracheitis, calicivirus and panleucopenia components, and 2 weeks after primary vaccination course for feline leukaemia component. the duration of immunity is one year after the last re-vaccination for the feline leukaemia component, and one year after primary vaccination course and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.

Unia Europejska - słowacki - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains), attenuated feline panleucopenia virus (pli iv), felv recombinant canarypox virus (vcp97), attenuated chlamydophila felis (905 strain) - immunologicals pre felidae, - mačky - active immunisation of cats aged 8 weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs;against chlamydophila felis infection to reduce clinical signs;against feline panleucopenia to prevent mortality and clinical signs;against leukaemia to prevent persistent viraemia and clinical signs of the related disease. onsets of immunity are 1 week after primary vaccination course for rhinotracheitis, calicivirus, chlamydophila felis and panleucopenia components, and 2 weeks after primary vaccination course for feline leukaemia component. the duration of immunity is one year after the last re-vaccination for the chlamydiosis and feline leukaemia components, and one year after primary vaccination course and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.

Unia Europejska - słowacki - EMA (European Medicines Agency)

ceva-phylaxia co. ltd. - live recombinant fowlpox virus expressing the membrane fusion protein and the encapsidation protein of avian infectious laryngotracheitis virus (rfp-lt) and avian encephalomyelitis virus, strain calnek 1143 (ae) - immunologicals for aves, live viral vaccines, domestic fowl - kura - for active immunisation of chickens of 8 to 13 weeks of age in order to reduce the skin lesions due to fowlpox, to reduce the clinical signs and tracheal lesions due to avian infectious laryngotracheitis and to prevent egg production losses due to avian encephalomyelitis.

Unia Europejska - słowacki - EMA (European Medicines Agency)

virbac s.a. - purified p45 feline leukaemia virus envelope antigen, live feline calicivirus (strain f9), live feline viral rhinotracheitis virus (strain f2), live feline panleucopenia virus - live mačací panleucopenia virus / parvovirus + live mačací dobytka vírus + live mačací calicivirus + inaktivované mačací vírus leukémie - mačky - na aktívnu imunizáciu mačiek od veku ôsmich týždňov proti: kaliciviróze mačiek na zníženie klinických príznakov. mačacej vírusovej rinotracheitídy na zníženie klinických príznakov a vírusovej exkrécie. mačacej panleukopénie na prevenciu leukopénie a na zníženie klinických príznakov. mačacej leukémie, aby sa zabránilo pretrvávajúcej virémii a klinickým príznakom súvisiacej choroby. nástup imunity: 3 týždňov po základnej očkovania pre panleucopenia a leukémia komponentov a 4 týždne po základnej očkovania pre calicivirus a dobytka vírus komponentov. trvanie imunity: jeden rok po primárnej vakcinácii pre všetky zložky.

Unia Europejska - słowacki - EMA (European Medicines Agency)

merck sharp & dohme b.v.  - osýpky vírus enders' edmonston kmeň (live, oslabenej), mumps vírus jeryl lynn (úroveň b) kmeň (live, oslabenej), rubeola vírus wistar ra 27/3 kmeň (live, oslabenej) - rubella; mumps; immunization; measles - vakcíny - m-m-rvaxpro je určený pre súčasné očkovanie proti osýpky, mumps a rubeola v jednotlivci 12 mesiacov alebo viac,. pre použitie v osýpky ohniska, alebo po skončení expozície očkovania, alebo pre použitie v minulosti nevakcinované detí starších ako 12 mesiacov, ktorí sú v kontakte s náchylné tehotné ženy a osoby, ktoré pravdepodobne citlivé na mumps a rubeola.