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

celvapan

nanotherapeutics bohumil, s.r.o. - whole virion influenza vaccine, inactivated containing antigen of strain a/california/07/2009 (h1n1)v - disease outbreaks; influenza, human; immunization - vaċċini - profilassi tal-influwenza kkawżata mill-virus a (h1n1) v 2009. celvapan ma għandu jintuża skont il-gwida uffiċjali.

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

procomvax

sanofi pasteur msd, snc - polyribosylribitol phosphate mill-haemophilus influenzae tat-tip b bħala prp-ompc, il-membrana ta 'barra kumpless tal-proteina tal neisseria meningitidis (il-membrana ta' barra kumpless tal-proteina tar-razza b11 ta 'neisseria meningitidis sottogrupp b), adsorbit ta' l-epatite b-antiġen tal-wiċċ prodott f'ċelloli tal-ħmira rikombinanti (saccharomyces cerevisiae) - hepatitis b; meningitis, haemophilus; immunization - vaċċini - procomvax huwa indikat għall-vaċċinazzjoni kontra l-marda invażivi ikkawżat minn influwenza Ħemofillika tip b u kontra l-infezzjoni kkawżat mill-sottotipi magħrufa kollha tal-virus tal-hepatitis b fit-trabi 6 ġimgħat sa 15-il xahar.

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

menquadfi

sanofi pasteur - neisseria meningitidis group c polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group a polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group y polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group w-135 polysaccharide conjugated to tetanus toxoid - meninġite, meningokokkali - vaċċini - menquadfi is indicated for active immunisation of individuals from the age of 12 months and older against invasive meningococcal disease caused by neisseria meningitidis serogroups a, c, w, and y. the use of this vaccine should be in accordance with available official recommendations.

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.