Unjoni Ewropea - Svediż - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains) - immunologicals för kattdjur, - katter - active immunisation of cats aged eight weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs. onsets of immunity isone week after primary vaccination course. the duration of immunity is one year after primary vaccination course and three years after the last re-vaccination.

Unjoni Ewropea - Svediż - EMA (European Medicines Agency)

merial - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains), attenuated chlamydophila felis (905 strain) - immunologicals för kattdjur, - katter - active immunisation of cats aged 8 weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs and excretion;against chlamydophila felis infection to reduce clinical signs. immunitetens intrång har visats 1 vecka efter primärvaccinationskurs för rinotrakeit, kalicivirus och chlamydophila felis-komponenter. varaktigheten av immunitet är 1 år efter den sista (re) vaccinationen.

Unjoni Ewropea - Svediż - 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 för kattdjur, - katter - 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.

Unjoni Ewropea - Svediż - 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 chlamydophila felis (905 strain), attenuated feline panleucopenia virus (pli iv) - immunologicals för kattdjur, - katter - 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. immunitetens intrång har visats en vecka efter primärvaccinationskurs för rinotrakeit, kalicivirus, chlamydophila felis och panleukopeni-komponenter. 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.

Unjoni Ewropea - Svediż - 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 för kattdjur, - katter - 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.

Żvezja - Svediż - Läkemedelsverket (Medical Products Agency)

intervet international b.v. - rabiesvirus, stam pasteur riv, inaktiverat - injektionsvätska, suspension - 2 ie - tiomersal hjälpämne; aluminiumfosfat 3 mg adjuvans; rabiesvirus, stam pasteur riv, inaktiverat 2 ie aktiv substans - rabiesvirus - får, get, hund, häst, iller, katt, nöt, räv

Żvezja - Svediż - Läkemedelsverket (Medical Products Agency)

europharmadk aps - rabiesvirus, stam pasteur riv, inaktiverat - injektionsvätska, suspension - 2 ie - tiomersal hjälpämne; glukos (vattenfri) hjälpämne; rabiesvirus, stam pasteur riv, inaktiverat 2 ie aktiv substans; aluminiumfosfat 3 mg adjuvans - rabiesvirus - får, get, hund, häst, iller, katt, nöt, räv

Żvezja - Svediż - Läkemedelsverket (Medical Products Agency)

boehringer ingelheim animal health denmark a/s - newcastlesjukevirus, stam ulster 2c, inaktiverat; egg drop syndrome virus (eds-76), stam v127, inaktiverat; infektiöst fågelbronkitvirus, typ massachusetts, stam m41, inaktiverat - injektionsvätska, emulsion - paraffin, flytande 170 - 186 mg adjuvans; newcastlesjukevirus, stam ulster 2c, inaktiverat 50 pd50 aktiv substans; infektiöst fågelbronkitvirus, typ massachusetts, stam m41, inaktiverat 18 hie aktiv substans; egg drop syndrome virus (eds-76), stam v127, inaktiverat 180 hie aktiv substans; tiomersal hjälpämne - newcastlesjukevirus / paramyxovirus + aviärt infektiöst bronkitvirus + aviärt adenovirus - fjäderfä

Żvezja - Svediż - Läkemedelsverket (Medical Products Agency)

boehringer ingelheim animal health denmark a/s - newcastlesjukevirus, stam ulster 2c, inaktiverat; egg drop syndrome virus (eds-76), stam v127, inaktiverat; fågelrhinotrakeitvirus, stam vc03, inaktiverat; infektiöst fågelbronkitvirus, typ massachusetts, stam m41, inaktiverat - injektionsvätska, emulsion - fågelrhinotrakeitvirus, stam vc03, inaktiverat 60 ip aktiv substans; egg drop syndrome virus (eds-76), stam v127, inaktiverat 162 hie aktiv substans; infektiöst fågelbronkitvirus, typ massachusetts, stam m41, inaktiverat 18 hie aktiv substans; newcastlesjukevirus, stam ulster 2c, inaktiverat 50 pd50 aktiv substans; tiomersal hjälpämne - aviärt infektiöst bronkitvirus + newcastlesjukevirus/paramyxovirus + aviärt adenovirus + aviärt rhinotrakeitvirus - fjäderfä

Unjoni Ewropea - Svediż - EMA (European Medicines Agency)

glaxosmithkline biologicals s.a. - delad influensavirus inaktiverad, innehållande antigen som motsvarar a / california / 07/2009 (h1n1) -derad stam som användes nymc x-179a - influenza, human; immunization; disease outbreaks - influensavacciner - profylax av influensa orsakad av a (h1n1) v 2009 virus. pandemrix bör endast användas om de rekommenderade årliga trivalenta / kvadrivalenta säsongsinfluensa vaccinerna inte är tillgängligt och om immunisering mot (h1n1) v anses nödvändig (se avsnitt 4. 4 och 4. pandemrix ska användas i enlighet med officiella riktlinjer.