BOVALTO Respi 4 suspension for injection Irland - engelska - 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 Irland - engelska - 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 USA - engelska - 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

Trivalent influenza vaccine (split virion, inactivated) High Dose suspension for injection 0.5ml pre-filled syringes Storbritannien - engelska - MHRA (Medicines & Healthcare Products Regulatory Agency)

trivalent influenza vaccine (split virion, inactivated) high dose suspension for injection 0.5ml pre-filled syringes

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

Verorab, powder and solvent for suspension for injection.                                                                           Rabies vaccine, inactivated. Irland - engelska - HPRA (Health Products Regulatory Authority)

verorab, powder and solvent for suspension for injection. rabies vaccine, inactivated.

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

NOBILIS NEWCAVAC VACCINE AGAINST NEWCASTLE DISEASE IN POULTRY Australien - engelska - APVMA (Australian Pesticides and Veterinary Medicines Authority)

nobilis newcavac vaccine against newcastle disease in poultry

intervet australia pty limited - inactivated newcastle disease virus antigen - misc. vaccines or anti sera - inactivated newcastle disease virus antigen vaccine-viral active 0.0 p - immunotherapy - poultry | breeders | broiler | chickens | chicks | chooks | day old chicks | hatchlings | layers - newcastle disease | vaccine | equine rotavirus

INACTIVATED INFLUENZA VACCINE (SPLIT VIRION) BP, suspension for injection in prefilled syringe.Influenza vaccine (split virion, Irland - engelska - HPRA (Health Products Regulatory Authority)

inactivated influenza vaccine (split virion) bp, suspension for injection in prefilled syringe.influenza vaccine (split virion,

sanofi pasteur - a/michigan/45/2015 (h1n1)pdm09 - like strain (a/michigan/45/2015, nymc x-275); a/hong kong/4801/2014 (h3n2) - like strain (a/hong kong/4801/2014, nymc x-263b); b/brisbane/60/2008 - like strain (b/brisbane/60/2008) - suspension for injection - 15/15/15mc percent volume/volume - influenza vaccines; influenza, inactivated, split virus or surface antigen

Rabies Vaccine BP > 2.5 IU/ml, Powder and solvent for suspension for injection Irland - engelska - HPRA (Health Products Regulatory Authority)

rabies vaccine bp > 2.5 iu/ml, powder and solvent for suspension for injection

sanofi pasteur - inactivated rabies virus strain pm/wi 38 1503 3m - powder and solvent for suspension for injection - 2.5 international unit(s)/millilitre - rabies vaccines; rabies, inactivated, whole virus

Imovax Polio Suspension For Injection (IM/SC) Filippinerna - engelska - FDA (Food And Drug Administration)

imovax polio suspension for injection (im/sc)

n/a; importer: sanofi pasteur, inc.; distributor: n/a - inactivated poliomyelitis vaccine (type 1,2 and 3) - suspension for injection (im/sc) - formulation: one dose (0.5 ml) contains: poliovirus type 1, mahoney strain (inactivated)-40 d-antigen units poliovirus type 2, mff-i strain (inactivated)- 8 d-antigen units poliovirus type 3, saukett strain (inactivated) - 32 d-antigen units

Equilis West Nile Europeiska unionen - engelska - EMA (European Medicines Agency)

equilis west nile

intervet international bv - inactivated chimaeric flavivirus strain yf-wn - immunologicals - horses - active immunisation of horses against west nile virus (wnv) to reduce clinical signs of disease and lesions in the brain and to reduce viraemia. onset of immunity: 2 weeks after primary vaccination course of two injections. duration of immunity: 12 months.,