Irland - engelsk - HPRA (Health Products Regulatory Authority)

sanofi pasteur msd ltd - strain cr 326f hepatitis a virus, inactivated 50 u - solution for injection - 50iu/1ml units/ml - hepatitis vaccines

Irland - engelsk - HPRA (Health Products Regulatory Authority)

sanofi pasteur msd ltd - hepatitis a vaccine - solution for injection - 25iu/0.5 m units/ml - hepatitis vaccines

Irland - engelsk - HPRA (Health Products Regulatory Authority)

sanofi pasteur msd ltd - varicella virus (oka strain) live attenuated - pdr+solv for susp for inj - > 1350 pfu - varicella zoster vaccines

Irland - engelsk - HPRA (Health Products Regulatory Authority)

sanofi pasteur msd ltd - pneumococcal polysaccharide serotype 1, pneumococcal polysaccharide type 2 (2), pneumococcal polysaccharide type 3 (3), pneumococcal polysaccharide serotype 4, pneumococcal polysaccharide serotype 5, pneumococcal polysaccharide serotype 6b, pneumococcal polysaccharide serotype 7f, pneumococcal polysaccharide type 8 (8), pneumococcal polysaccharide type 9n, pneumococcal polysaccharide serotype 9v, pneumococcal polysaccharide type 20 (20), pneumococcal oligosaccharide serotype 18c, pneumococcal polysaccharide - solution for injection in pre-filled syringe - 25/0.5 microgram/ml - pneumococcal vaccines - it is recommended for active immunisation against disease caused by the pneumococcal serotypes included in the vaccine

Irland - engelsk - HPRA (Health Products Regulatory Authority)

sanofi pasteur msd ltd - diphtheria toxoid, tetanus toxoid, pertussis toxoid, filamentous haemagglutinin, pertactin (prn), fimbriae types 2 and 3 - suspension for injection - pertussis, purified antigen, combinations with toxoids

Irland - engelsk - HPRA (Health Products Regulatory Authority)

sanofi pasteur msd ltd - haemophilus influenzae type b, conjugate with tetanus protein - pdr+solv for soln for inj - 10mcg/0.5m microgram/ml - hemophilus influenzae b vaccines

Irland - engelsk - HPRA (Health Products Regulatory Authority)

sanofi pasteur msd ltd - tetanus toxoid, diphtheria toxoid, pertussis toxoid, filamentous haemagglutinin (fha), pertactin, polio virus type 1 inactivated, polio virus type 2 inactivated, polio virus type 3 inactivated, adsorbed fimbriae types 2 + 3 - suspension for injection - unknown - bacterial and viral vaccines, combined

Irland - engelsk - HPRA (Health Products Regulatory Authority)

sanofi pasteur msd ltd - tetanus toxoid, diphtheria toxoid, pertussis toxoid, filamentous haemagglutinin, pertactin, fimbriae types 2 and 3, adsorbed aluminium phosphate - suspension for injection - pertussis, purified antigen, combinations with toxoids

Irland - engelsk - HPRA (Health Products Regulatory Authority)

sanofi pasteur msd ltd - a/california/7/2009/(h1n1)pdm - like strain (a/california/7/2009, nymc x-179a), a/texas/50/2012/(h3n2) - like strain (a/texas/50/2012, nymc x-223a), b/brisbane/60/2008 (victoria lineage), b/massachussets/2/2012 (yamagata lineage) - solution for injection in pre-filled syringe - 15 microgram - influenza vaccines

Storbritannia - engelsk - MHRA (Medicines & Healthcare Products Regulatory Agency)

sanofi pasteur msd ltd - human poliovirus type 3 inactivated; tetanus toxoid; pertussis antigens; human poliovirus type 1 inactivated; human poliovirus type 2 inactivated; diphtheria toxoid; haemophilus influenzae type b polysaccharide protein conjugate - suspension for injection