RotaTeq Unjoni Ewropea - Malti - EMA (European Medicines Agency)

rotateq

merck sharp & dohme b.v. - rotavirus serotip g1, serotip g2, serotip g3, serotip g4, serotip p1 - immunization; rotavirus infections - vaccines, viral vaccines - rotateq huwa indikat għall-immunizzazzjoni attiva tat-trabi mill-età ta 'sitt ġimgħat sa 32 ġimgħa għall-prevenzjoni ta' gastroenterite minħabba infezzjoni ta 'rotavirus. rotateq għandu jintuża fuq il-bażi ta ' rakkomandazzjonijiet uffiċjali.

Trumenba Unjoni Ewropea - Malti - EMA (European Medicines Agency)

trumenba

pfizer europe ma eeig - neisseria meningitidis serogroup b fhbp (fhbp lipidat rikombinanti (proteina li jgħaqqad il-fattur h)) subfamilja a; neisseria meningitidis serogroup b fhbp (fhbp lipidat rikombinanti (proteina li jgħaqqad il-fattur h)) subfamilja b - meninġite, meningokokkali - bacterial vaccines, meningococcal vaccines - trumenba huwa indikat għall-immunizzazzjoni attiva ta 'individwi ta' 10 snin jew aktar biex jipprevjenu mard meningokokkali invażiv ikkawżat minn neisseria meningitidis serogroup b. l-użu ta ' dan il-vaċċin għandha tkun skond ir-rakkomandazzjonijiet uffiċjali.

Humenza Unjoni Ewropea - Malti - EMA (European Medicines Agency)

humenza

sanofi pasteur s.a. - qasma-virus tal-influwenza, inattivat, li fih antiġen*:/california/7/2009 (h1n1)v like strain (x-179a)*propagati fil-bajd. - influenza, human; immunization; disease outbreaks - vaċċini - profilassi tal-influwenza f'sitwazzjoni pandemika ddikjarata uffiċjalment. vaċċin għal influwenza pandemika għandu jintuża skont il-gwida uffiċjali.

Coliprotec F4/F18 Unjoni Ewropea - Malti - EMA (European Medicines Agency)

coliprotec f4/f18

elanco gmbh - escherichia coli ħajjin mhux patoġeniċi o141: k94 (f18ac) u o8: k87 (f4ac) - immunologicals for suidae, live bacterial vaccines - majjali - għall-immunizzazzjoni attiva tal-majjali minn 18-il jum ta'l-età kontra l-enterotoxigenic f4-pożittivi u f18-pożittivi escherichia coli sabiex titnaqqas l-inċidenza ta moderat għal sever ta ' wara l-ftim e. coli diarrhea (pwd) fil-ħnieżer infettati u biex jitnaqqas it-tixrid tal-feċi ta 'e-enterotoxigenic f4 pożittiv u e pożittiv f18. coli minn ħnieżer infettati.

Coxevac Unjoni Ewropea - Malti - EMA (European Medicines Agency)

coxevac

ceva santé animale - vaċċin inattivat ta 'coxiella burnetii, strain 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 Unjoni Ewropea - Malti - 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) - tnaqqis ta 'enterotossikożi tat-twelid tal-ħnienes, ikkawżat minn e. coli strains, li jesprimu l-adesini f4ab, f4ac, f4ad, f5, f6 u f41, matul l-ewwel jiem tal-ħajja.

Porcilis AR-T DF Unjoni Ewropea - Malti - EMA (European Medicines Agency)

porcilis ar-t df

intervet international bv - protein do (mhux tossiku t-tħassir tad-derivattivi ta ' pasteurella multocida dermonecrotic-tossina), inattivati tal-bordetella bronchiseptica-ċelluli - immunoloġiċi għal suidae - majjali (ħnieżer nisa u majjali nisa) - għat-tnaqqis ta 'sinjali kliniċi ta' rinite atrofika progressiva fil-qżieqeż permezz ta 'immunizzazzjoni passiva orali bil-kolostru minn digi immjunizzati b'mod attiv bil-vaċċin.

Porcilis PCV ID Unjoni Ewropea - Malti - EMA (European Medicines Agency)

porcilis pcv id

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.

ProteqFlu-Te Unjoni Ewropea - Malti - EMA (European Medicines Agency)

proteqflu-te

boehringer ingelheim vetmedica gmbh - clostridium tetani toxoid / kvp 2242 virus / vcp1529 virus / għal vcp1533 għal virus / vcp3011 virus - immunologicals for equidae, live viral and inactivated bacterial vaccines, equine influenza virus + clostridium - Żwiemel - immunizzazzjoni attiva ta 'żwiemel ta' erba 'xhur jew akbar kontra l-influwenza taż-żwiemel biex jitnaqqsu s-sinjali kliniċi u l-eskrezzjoni tal-virus wara infezzjoni, u kontra t-tetnu biex tiġi evitata l-mortalità.

Suvaxyn CSF Marker Unjoni Ewropea - Malti - 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 - majjali - għal immunizzazzjoni attiva ta 'majjali minn 7 ġimgħat' il quddiem biex tevita l-mortalità u tnaqqas l-infezzjoni u l-mard ikkawżat mill-virus tad-deni klassiku tal-ħnieżer (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.