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Our vaccines portfolio
Boostrix
Diphtheria, tetanus and pertussis
(acellular, component) vaccine
(adsorbed, reduced antigen(s) content)
IPV‐Boostrix
Diphtheria, tetanus, pertussis (acellular, component) and poliomyelitis (inactivated) vaccine (adsorbed, reduced antigen(s) content)
Cervarix
Human Papillomavirus vaccine [Types 16, 18] (Recombinant, adjuvanted, adsorbed)
Engerix B 20mcg (Adult)
Hepatitis B (rDNA) vaccine (adsorbed) (HBV)
Engerix B 10mcg (Paediatric)
Hepatitis B (rDNA) vaccine (adsorbed) (HBV)
Hepatitis B (rDNA) vaccine (adjuvanted, adsorbed)
Hepatitis A Vaccine
(inactivated, adsorbed)
Hepatitis A Vaccine
(inactivated, adsorbed)
Hiberix
Haemophilus Type b (Hib) vaccine
Infanrix Hexa
Diphtheria (D), tetanus (T),
pertussis (acellular, component) (Pa), hepatitis B (rDNA) (HBV), poliomyelitis (inactivated) (IPV) and Haemophilus influenzae type b (Hib) conjugate vaccine (adsorbed)
Menitorix
Haemophilus type b and Meningococcal group C conjugate vaccine
Menjugate
Meningococcal group C conjugate vaccine
Menveo
Meningococcal Group A, C, W135 and Y conjugate vaccine
Measles, Mumps and Rubella vaccine (live)
rotavirus vaccine, live
Hepatitis A (inactivated) and hepatitis B (rDNA) (HAB) vaccine (adsorbed)
Hepatitis A (inactivated) and hepatitis B (rDNA) (HAB) vaccine (adsorbed)
Adverse events should be reported directly to the HPRA; Freepost, Pharmacovigilance Section, Health Products Regulatory Authority, Earlsfort Terrace, Dublin 2, Tel: +353 1 676 4971 medsafety@hpra.ie. Adverse events should also be reported to GlaxoSmithKline on 1800 244 255.
Bexsero, Boostrix, IPV-Boostrix, Cervarix, Engerix B, Fendrix, Havrix, Hiberix, Infanrix Hexa, Menitorix, Menjugate, Menveo, Priorix, Rotarix and Twinrix are registered trademarks of the GlaxoSmithKline Group of Companies.
