Purevax RCP FeLV Umoja wa Ulaya - Kiholanzi - EMA (European Medicines Agency)

purevax rcp felv

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 voor felidae, - cats - 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.

Purevax RCPCh Umoja wa Ulaya - Kiholanzi - EMA (European Medicines Agency)

purevax rcpch

boehringer ingelheim vetmedica gmbh - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains), attenuated chlamydophila felis (905 strain), attenuated feline panleucopenia virus (pli iv) - immunologicals voor felidae, - cats - active immunisation of cats aged eight 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. onsets van immuniteit zijn aangetoond een week na de primaire vaccinatiekuur voor rhinotracheitis, calicivirus, chlamydophila felis en panleucopenie componenten. the duration of immunity is one year after the last re-vaccination for the chlamydiosis component, and oneyear after primary vaccination and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.

Purevax RCPCh FeLV Umoja wa Ulaya - Kiholanzi - EMA (European Medicines Agency)

purevax rcpch felv

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 voor felidae, - cats - 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.

Fixr APP 2,9,11 emulsie voor injectie voor varkens Uholanzi - Kiholanzi - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

fixr app 2,9,11 emulsie voor injectie voor varkens

kernfarm b.v. - !!zie spc; geÏnactiveerd actinobacillus pleuropneumoniae, serotype 2; geÏnactiveerd actinobacillus pleuropneumoniae, serotype 2 stam sz ii; geÏnactiveerd actinobacillus pleuropneumoniae, serotype 9 - emulsie voor injectie - actinobacillus/haemophilus vaccine - varkens

PreHevbri Umoja wa Ulaya - Kiholanzi - EMA (European Medicines Agency)

prehevbri

vbi vaccines b.v. - hepatitis b-oppervlakte-antigeen - hepatitis b - vaccins - prehevbri is indicated for active immunisation against infection caused by all known subtypes of the hepatitis b virus in adults. it can be expected that hepatitis d will also be prevented by immunisation with prehevbri as hepatitis d (caused by the delta agent) does not occur in the absence of hepatitis b infection. the use of prehevbri should be in accordance with official recommendations.

Acticarp cattle 50 mg/ml Oplossing voor injectie voor runderen Uholanzi - Kiholanzi - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

acticarp cattle 50 mg/ml oplossing voor injectie voor runderen

accord healthcare b.v. - carprofen - oplossing voor injectie - carprofen 50 mg/ml, - carprofen - runderen

Amoxy Active CTD 697 mg/g, poeder voor gebruik in drinkwater voor kippen, kalkoenen en eenden Uholanzi - Kiholanzi - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

amoxy active ctd 697 mg/g, poeder voor gebruik in drinkwater voor kippen, kalkoenen en eenden

dopharma research b.v. - amoxicilline 0-water - poeder voor gebruik in drinkwater - amoxicilline 0-water 697 mg/g, - amoxicillin - eenden; kalkoenen; kippen

Bovilis IBR Marker Live nas. susp. (lyof. + oplosm.)/inj. susp. (lyof. + oplosm.) i.m. flac. Ubelgiji - Kiholanzi - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

bovilis ibr marker live nas. susp. (lyof. + oplosm.)/inj. susp. (lyof. + oplosm.) i.m. flac.

intervet international - levend boviene herpesvirus type 1 (bhv1) 5,7 log10 tcid50/dose - lyofilisaat en oplosmiddel voor suspensie voor nasaal gebruik; lyofilisaat en oplosmiddel voor suspensie voor injectie - levend boviene herpesvirus type 1 (bhv1) - bovine viral diarrhea (bvd) - rund

Bovilis IBR Marker Live inj. susp. (lyof. + oplosm.)/nas. susp. (lyof. + oplosm.) i.m. flac. Ubelgiji - Kiholanzi - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

bovilis ibr marker live inj. susp. (lyof. + oplosm.)/nas. susp. (lyof. + oplosm.) i.m. flac.

intervet international - levend boviene herpesvirus type 1 (bhv1) 5,7 log10 tcid50/dose - lyofilisaat en oplosmiddel voor suspensie voor nasaal gebruik; lyofilisaat en oplosmiddel voor suspensie voor injectie - levend boviene herpesvirus type 1 (bhv1) - bovine viral diarrhea (bvd) - rund

Bovilis INtranasal RSP Live neusspray susp. (lyof. + oplosm.) flac. Ubelgiji - Kiholanzi - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

bovilis intranasal rsp live neusspray susp. (lyof. + oplosm.) flac.

intervet international b.v. - levend, geattenueerd, boviene parainfluenza-3-virus ; levend, geattenueerd, boviene respiratory syncytial-virus (brsv) - neusspray, lyofilisaat en oplosmiddel voor suspensie - gemodificeerd levend boviene parainfluenza-3-virus; boviene respiratory syncytial-virus (brsv) - bovine respiratory syncytial virus + bovine parainfluenza virus - rund