यूरोपीय संघ - माल्टीज़ - EMA (European Medicines Agency)

intervet international b.v. - Ċirovirus tal-porċini tat-tip 2 ta 'l-antiġen tat-tip subunit orf2 - immunologicals for suidae, inactivated viral vaccines - majjali - 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.

यूरोपीय संघ - माल्टीज़ - EMA (European Medicines Agency)

intervet international b.v. - Ċirkovirus tal-ħnieżer tat-tip 2 (pcv2) orf2 subunit tal-antiġen, mycoplasma hyopneumoniae j razza inattivat - immunologicals for suidae, inactivated viral and inactivated bacterial vaccines - Ħnieżer (għall-tismin) - għal-immunizzazzjoni attiva tal-ħnieżer biex jitnaqqas viremija, viral load fil-pulmuni u fit-tessuti limfodje, virus jixħtu kkawżata mill-virus porcine circovirus tip 2 (pcv2) l-infezzjoni, u s-severità tal-pulmun tal-leżjonijiet ikkawżati minn mycoplasma hyopneumoniae infezzjoni. biex tnaqqas it-telf ta 'żieda fil-piż ta' kuljum matul il-perjodu ta 'tlestija f'każ ta' infezzjonijiet b'mycoplasma hyopneumoniae u / jew pcv2 (kif osservat fi studji fuq il-post).

यूरोपीय संघ - माल्टीज़ - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains) - immunoloġiċi għall-felini, - qtates - 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.

यूरोपीय संघ - माल्टीज़ - 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) - immunoloġiċi għall-felini, - qtates - 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. Ġew murija onsets ta 'immunità 1 ġimgħa wara l-kors ta' tilqim primarju għal rinotrakeite, kaliċivirus u komponenti ta 'chlamydophila felis. it-tul ta 'l-immunità huwa ta' sena wara l-aħħar vaċċinazzjoni (mill-ġdid).

यूरोपीय संघ - माल्टीज़ - 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) - immunoloġiċi għall-felini, - qtates - 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.

यूरोपीय संघ - माल्टीज़ - EMA (European Medicines Agency)

glaxosmithkline biologicals s.a. - diphtheria toxoid, hepatitis b surface antigen, bordetella pertussis (inactivated), tetanus toxoid - hepatitis b; tetanus; immunization; whooping cough; diphtheria - vaċċini - tritanrix hepb huwa indikat għal immunizzazzjoni attiva kontra d-difterite, it-tetnu, it-pertussis u l-epatite b (hbv) fit-trabi minn sitt ġimgħat 'il quddiem (ara sezzjoni 4.

यूरोपीय संघ - माल्टीज़ - EMA (European Medicines Agency)

zoetis belgium sa - ċirkovirus tal-ħnieżer-vaċċin (inattivat, rikombinanti) - immunologicals for suidae, inactivated viral vaccines - Ħnieżer (għall-tismin) - għall-immunizzazzjoni attiva tal-ħnieżer mill-età ta ' 3 ġimgħat kontra l-virus porcine circovirus tip 2 (pcv2) biex titnaqqas it-tagħbija virali fid-demm u fit-tessuti linfojde u l-ippurgar jixħtu kkawżati mill-infezzjoni bil-pcv2.

यूरोपीय संघ - माल्टीज़ - EMA (European Medicines Agency)

ceva santé animale - clostridium perfringens type c, beta1 toxoid / clostridium perfringens, type a, alpha toxoid / clostridium perfringens, type a, beta2 toxoid / escherichia coli, fimbrial adhesin f4ab / escherichia coli, fimbrial adhesin f4ac / escherichia coli, fimbrial adhesin f5 / escherichia coli, fimbrial adhesin f6 - immunologicals for suidae, inactivated bacterial vaccines (including mycoplasma, toxoid and chlamydia) escherichia + clostridium - majjali - for the passive immunisation of progeny by active immunisation of pregnant sows and gilts to reduce:-           clinical signs (severe diarrhoea) and mortality caused by escherichia coli strains expressing the fimbrial adhesins f4ab, f4ac, f5 and f6-           clinical signs (diarrhoea during the first days of life) associated with clostridium perfringens type a expressing alpha and beta 2 toxins-           clinical signs and mortality associated with haemorrhagic and necrotising enteritis caused by clostridium perfringens type c expressing beta1 toxin.

यूरोपीय संघ - माल्टीज़ - EMA (European Medicines Agency)

laboratorios hipra, s.a. - clostridioides difficile toxoid a, clostridioides difficile toxoid b, clostridium perfringens, type a, alpha toxoid - immunologicals for suidae, inactivated bacterial vaccines for pigs, clostridium - majjali - for the passive immunisation of neonatal piglets by means of the active immunisation of breeding sows and gilts:- to prevent mortality and reduce clinical signs and macroscopic lesions caused by clostridioides difficile toxins a and b. - to reduce clinical signs and macroscopic lesions caused by clostridium perfringens type a, alpha toxin.

यूरोपीय संघ - माल्टीज़ - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - massimu ta'tliet minn dawn li ġejjin purifikat, inattivat tal-marda tal-ilsien u d-dwiefer-virus tal-marda razez: o1 manisa ≥ 6 pd50*; o1 bfs ≥ 6 pd50*; o t-tajwan 3/97 ≥ 6 pd50*; a22-iraq ≥ 6 pd50*; a24 cruzeiro ≥ 6 pd50*; turkija 14/98 ≥ 6 pd50*; l-asja 1 shamir ≥ 6 pd50*; sat2 l-għarabja sawdita ≥ 6 pd50*; * pd50 – 50% protettiv-doża fl-ifrat kif deskritt fil-ph. eur. monografija 0063. - immunoloġiċi - pigs; cattle; sheep - immunizzazzjoni attiva ta 'baqar, nagħaġ u majjali minn età ta' 2 ġimgħat kontra l-marda ta 'l-ilsien u d-dwiefer biex jitnaqqsu s-sinjali kliniċi.