Equilis StrepE Evropska unija - malteščina - EMA (European Medicines Agency)

equilis strepe

intervet international bv - streptococcus equi strain mutant tat-tħassir ħaj tw928 - immunoloġiċi għall-equidae - Żwiemel - għall-immunizzazzjoni taż-żwiemel kontra streptococcus equi biex tnaqqas is-sinjali kliniċi u l-okkorrenza tal-limfa-axxesi. il-bidu tal-immunità: il-bidu tal-immunità huwa stabbilit ġimagħtejn wara t-tilqima bażika. tul ta 'żmien tal-immunità: it-tul tal-immunità huwa ta' tliet xhur. il-vaċċin huwa maħsub għall-użu fiż-żwiemel li għalihom ġie identifikat b'mod ċar riskju ta 'infezzjoni streptococcus equi, minħabba kuntatt ma' żwiemel minn żoni fejn dan il-patoġenu hu magħruf li hu preżenti, e. stalel ma 'żwiemel li jivvjaġġaw għal wirjiet jew kompetizzjonijiet f'dawn iż-żoni, jew stalel li jakkwistaw jew ikollhom żwiemel tal-livery minn dawk iż-żoni.

Zabdeno Evropska unija - malteščina - EMA (European Medicines Agency)

zabdeno

janssen-cilag international n.v.    - recombinant adenovirus type 26 (ad26) encoding the glycoprotein (gp) of the ebola virus zaire (zebov) mayinga strain - emorraġiku-deni, l-ebola - vaċċini - active immunization for prevention of disease caused by ebola virus (zaire ebolavirus species) in individuals ≥ 1 year of age.

Spikevax (previously COVID-19 Vaccine Moderna) Evropska unija - malteščina - EMA (European Medicines Agency)

spikevax (previously covid-19 vaccine moderna)

moderna biotech spain, s.l. - single-stranded, 5’-capped messenger rna (mrna) produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - vaċċini - spikevax is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older. spikevax bivalent original/omicron ba. 1 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 years of age and older who have previously received at least a primary vaccination course against covid-19. spikevax bivalent original/omicron ba. 4-5 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older.  spikevax xbb. 5 is indicated for active immunisation to prevent covid 19 caused by sars-cov-2 in individuals 6 months of age and older. the use of this vaccine should be in accordance with official recommendations.

Prevexxion RN Evropska unija - malteščina - EMA (European Medicines Agency)

prevexxion rn

boehringer ingelheim vetmedica gmbh - live recombinant marek’s disease (md) virus, serotype 1, strain rn1250 - immunoloġiċi għall-għasafar - chicken - for active immunisation of one-day-old chicks to prevent mortality and clinical signs and reduce lesions caused by marek’s disease (md) virus (including very virulent md virus).

CircoMax Myco Evropska unija - malteščina - EMA (European Medicines Agency)

circomax myco

zoetis belgium - inactivated mycoplasma hyopneumoniae, strain p-5722-3, inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2a open reading frame 2 (orf2) protein, inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2b orf2 protein - immunoloġiċi għal suidae - Ħnieżer (għall-tismin) - active immunisation of pigs against porcine circovirus type 2 to reduce viral load in blood and lymphoid tissues, fecal shedding and the lesions in lymphoid tissues associated with pcv2 infection. protection was demonstrated against porcine circovirus types 2a, 2b and 2d. active immunisation of pigs against mycoplasma hyopneumoniae to reduce the lung lesions associated with mycoplasma hyopneumoniae infection.  onset of immunity (both vaccination schedules): 3 weeks after (the last) vaccination.  duration of immunity (both vaccination schedules): 23 weeks after (the last) vaccination.  in addition, vaccination has been shown to reduce body weight gain losses under field conditions.

Humenza Evropska unija - malteščina - 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.

Purevax RC Evropska unija - malteščina - EMA (European Medicines Agency)

purevax rc

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.

Purevax RCP FeLV Evropska unija - malteščina - 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) - 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.

Celvapan Evropska unija - malteščina - 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.

Innovax-ILT Evropska unija - malteščina - EMA (European Medicines Agency)

innovax-ilt

intervet international b.v. - herpesvirus tad-dundjan rikombinanti ħajjin assoċjat miegħu (strain hvt / ilt-138), li jesprimi l-glycoproteins gd u gi tal-virus tal-laryngotracheitis infettiva - immunoloġiċi għall-aves, vaċċini virali Ħajjin - chicken - għall-immunizzazzjoni attiva ta ' wieħed mill-flieles biex tnaqqas l-imwiet, sinjali kliniċi u leżjonijiet tal-minħabba li infezzjoni bl-infettiva tat-tjur laryngotracheitis (ilt) u l-virus tal-marda ta'marek (md) tal-virus.