BOVALTO RESPI 3 SUSPENSION FOR INJECTION FOR CATTLE Irlandia - angielski - HPRA (Health Products Regulatory Authority)

bovalto respi 3 suspension for injection for cattle

merial animal health limited - inactivated bovine respiratory syncytial virus, strain bio-24, inactivated bovine parainfluenza 3 virus, strain bio-23, inactivated mannheimia (pasteurella) haemolyica, a1 strain dsm 5283 - suspension for injection - unknown - inactivated viral and inactivated bacterial vaccines - bovine - immunological - inactivated vaccine

BOVALTO RESPI 4 SUSPENSION FOR INJECTION FOR CATTLE Irlandia - angielski - HPRA (Health Products Regulatory Authority)

bovalto respi 4 suspension for injection for cattle

merial animal health limited - inactivated bovine respiratory syncytial virus, strain bio-24, inactivated bovine parainfluenza 3 virus, strain bio-23, inactivated mannheimia haemolytica serotype a1 strain dsm 5283, inactivated bovine viral diarrhoea virus, strain bio-25 - suspension for injection - unknown - inactivated viral and inactivated bacterial vaccines - bovine - immunological - inactivated vaccine

Zulvac BTV Unia Europejska - angielski - EMA (European Medicines Agency)

zulvac btv

zoetis belgium sa - one of the following inactivated bluetongue virus strains:inactivated bluetongue virus, serotype 1, strain btv-1/alg2006/01 e1inactivated bluetongue virus, serotype 8, strain btv-8/bel2006/02inactivated bluetongue virus, serotype 4, strain spa-1/2004 - immunologicals, immunologicals for bovidae, inactivated viral vaccines, bluetongue virus, sheep - sheep; cattle - active immunisation of sheep from 6 weeks of age for the prevention of viraemia caused by bluetongue virus, serotypes 1 and 8, and for the reduction of viraemia caused by bluetongue virus, serotype 4 and active immunisation of cattle from 12 weeks of age for the prevention of viraemia caused by bluetongue virus, serotypes 1 and 8.

BOVALTO Respi 3 suspension for injection Irlandia - angielski - HPRA (Health Products Regulatory Authority)

bovalto respi 3 suspension for injection

merial animal health limited - inactivated bovine respiratory syncytial virus, strain bio-24, inactivated bovine parainfluenza 3 virus, strain bio-23, inactivated mannheimia (pasteurella) haemolyica, a1 strain dsm 5283 - suspension for injection - . - inactivated viral and inactivated bacterial vaccines - cattle - immunological - inactivated vaccine

BOVALTO Respi 4 suspension for injection Irlandia - angielski - HPRA (Health Products Regulatory Authority)

bovalto respi 4 suspension for injection

merial animal health limited - inactivated bovine respiratory syncytial virus, strain bio-24, inactivated bovine parainfluenza 3 virus, strain bio-23, inactivated mannheimia haemolytica serotype a1 strain dsm 5283, inactivated bovine viral diarrhoea virus, strain bio-25 - suspension for injection - . - inactivated viral and inactivated bacterial vaccines - cattle - immunological - inactivated vaccine

IMOCOLIBOV Irlandia - angielski - HPRA (Health Products Regulatory Authority)

imocolibov

merial animal health limited - inactivated e.coli (antigen k99), inactivated e.coli (antigen y), inactivated e.coli (antigen 31a), inactivated e.coli serotype 09, inactivated e.coli serotype 08, inactivated e.coli serotype 015, inactivated e.coli serotype 078, inactivated e.coli serotype 0101, inactivated e.coli serotype 00117 - suspension for injection - percent - inactivated bacterial vaccines and antisera qi04ac inactivated bacterial vaccines and antisera - cattle, sheep - immunological - inactivated vaccine

PENTACEL (diphtheria and tetanus toxoids and acellular pertussis adsorbed, inactivated poliovirus and haemophilus b conjugate- t Stany Zjednoczone - angielski - NLM (National Library of Medicine)

pentacel (diphtheria and tetanus toxoids and acellular pertussis adsorbed, inactivated poliovirus and haemophilus b conjugate- t

sanofi pasteur inc. - corynebacterium diphtheriae toxoid antigen (formaldehyde inactivated) (unii: irh51qn26h) (corynebacterium diphtheriae toxoid antigen (formaldehyde inactivated) - unii:irh51qn26h), clostridium tetani toxoid antigen (formaldehyde inactivated) (unii: k3w1n8yp13) (clostridium tetani toxoid antigen (formaldehyde inactivated) - unii:k3w1n8yp13), bordetella pertussis toxoid antigen (glutaraldehyde inactivated) (unii: f4tn0ipy37) (bordetella pertussis toxoid antigen (glutaraldehyde inactivated) - unii:f4tn0ipy37 - corynebacterium diphtheriae toxoid antigen (formaldehyde inactivated) 15 [lf] in 0.5 ml - pentacel® is a vaccine indicated for active immunization against diphtheria, tetanus, pertussis, poliomyelitis and invasive disease due to haemophilus influenzae type b. pentacel is approved for use as a four dose series in children 6 weeks through 4 years of age (prior to fifth birthday). a severe allergic reaction (eg, anaphylaxis) after a previous dose of pentacel or any other diphtheria toxoid, tetanus toxoid, or pertussis-containing vaccine, inactivated poliovirus vaccine or h. influenzae type b vaccine, or any ingredient of this vaccine is a contraindication to administration of pentacel. [see description (11). ] encephalopathy (eg, coma, decreased level of consciousness, prolonged seizures) within 7 days of a previous dose of a pertussis containing vaccine that is not attributable to another identifiable cause is a contraindication to administration of any pertussis-containing vaccine, including pentacel. progressive neurologic disorder, including infantile spasms, uncontrolled epilepsy, or progres

IMOCOLIBOV Irlandia - angielski - HPRA (Health Products Regulatory Authority)

imocolibov

boehringer ingelheim vetmedica gmbh - inactivated e.coli serotype 09; inactivated e.coli serotype 08; inactivated e.coli serotype 015; inactivated e.coli serotype 078; inactivated e.coli serotype 0101; inactivated e.coli serotype 00117; inactivated e.coli (antigen k99); inactivated e.coli (antigen y); inactivated e.coli (antigen 31a) - suspension for injection - . - inactivated bacterial vaccines and antisera; inactivated bacterial vaccines and antisera

Adjupanrix (previously Pandemic influenza vaccine (H5N1) (split virion, inactivated, adjuvanted) GlaxoSmithKline Biologicals) Unia Europejska - angielski - EMA (European Medicines Agency)

adjupanrix (previously pandemic influenza vaccine (h5n1) (split virion, inactivated, adjuvanted) glaxosmithkline biologicals)

glaxosmithkline biologicals s.a. - split influenza virus, inactivated, containing antigen: a/vietnam/1194/2004 (h5n1) like strain used (nibrg-14) - influenza, human, immunization, disease outbreaks - vaccines, - prophylaxis of influenza in an officially declared pandemic situation. pandemic influenza vaccine should be used in accordance with official guidance.,

AQUAVAC PD3 EMULSION FOR INJECTION, FOR ATLANTIC SALMON Irlandia - angielski - HPRA (Health Products Regulatory Authority)

aquavac pd3 emulsion for injection, for atlantic salmon

intervet ireland limited - inactivated salmon pancreas disease virus, inactivated infectious pancreatic necrosis virus, inactivated aeromonas salmonicida subsp. salmonicida - emulsion for injection - 75 - inactivated viral and inactivated bacterial vaccines - fish - (atlantic) salmon - immunological - inactivated vaccine