Ireland - English - HPRA (Health Products Regulatory Authority)

zoetis belgium s.a. - inactivated bovine rotavirus, strain 1005/78, inactivated bovine rotavirus, strain holland, inactivated bovine coronavirus, strain 800, inactivated e.coli k99/f41, strain s1091/83 - suspension for injection - inactivated bovine rotavirus vaccine + inactivated bovine coronavirus vaccine + inactivated escheri - bovine - immunological - inactivated vaccine

Ireland - English - HPRA (Health Products Regulatory Authority)

merck sharp & dohme ireland (human health) limited - strain cr 326f hepatitis a virus, inactivated 50 u - suspension for injection in pre-filled syringe - 50 u/1 millilitre(s) - hepatitis vaccines; hepatitis a, inactivated, whole virus

Ireland - English - HPRA (Health Products Regulatory Authority)

merck sharp & dohme ireland (human health) limited - strain cr 326f hepatitis a virus, inactivated 50 u - suspension for injection in pre-filled syringe - 25 u/0.5 millilitre(s) - hepatitis vaccines; hepatitis a, inactivated, whole virus

European Union - English - EMA (European Medicines Agency)

intervet international b.v. - inactivated leptospira strains: l. interrogans serogroup canicola serovar portland-vere (strain ca-12-000); l. interrogans serogroup icterohaemorrhagiae serovar copenhageni (strain ic-02-001); l. interrogans serogroup australis serovar bratislava (strain as-05-073); l. kirschneri serogroup grippotyphosa serovar dadas (strain gr-01-005) - immunologicals for canidae, inactivated bacterial vaccines (including mycoplasma, toxoid and chlamydia) - dogs - for active immunisation of dogs against:l. interrogans serogroup canicola serovar canicola to reduce infection and urinary excretion;l. interrogans serogroup icterohaemorrhagiae serovar copenhageni to reduce infection and urinary excretion;l. interrogans serogroup australis serovar bratislava to reduce infection;l. kirschneri serogroup grippotyphosa serovar bananal/lianguang to reduce infection and urinary excretion.

Ireland - English - HPRA (Health Products Regulatory Authority)

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

Ireland - English - HPRA (Health Products Regulatory Authority)

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

Ireland - English - HPRA (Health Products Regulatory Authority)

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

United States - English - NLM (National Library of Medicine)

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

United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

split virion, inactivated) high dose suspension for injection 0.5ml pre-filled syringes (sanofi pasteur - influenza virus inactivated split (h1n1, h3n2-like, b/brisbane/60/2008-like, strains) - suspension for injection

Ireland - English - HPRA (Health Products Regulatory Authority)

sanofi pasteur - rabies virus (inactivated) strain wistar (pm/wi 38-1503-3m) - powder and solvent for suspension for injection in pre-filled syringe - rabies, inactivated, whole virus