REPEVAX®
Available from October 2004, for pre-school use in children aged 4-5 years.
Abbreviated vaccine composition: dTaP/IPV (low-dose Diphtheria, Tetanus and Pertussin; inactivated Polio).
Contains:
- Purified Diphtheria toxoid (2 I.U.)
- Purified Tetanus toxoid (20 I.U.)
- Purified Pertussis toxoid (PT)
- Inactivated Polio virus, types 1/2/3 (40, 8 and 32 Dantigen units respectively)
- Aluminium phosphate
- Formaldehyde
- 2-phenoxyethanol (phenol) - a preservative
- Polysorbate 80 - an emulsifier
- Polyribosylribitol - an artificial sweetener
- The inactivated polio virus is cultured on Vero (African green monkey kidney) cells
- Neomycin, streptomycin and polymyxin B - antibiotics
Undesirable effects (as reported by Dept of Health and Aventis Pasteur®):
- Injection site pain; redness; swelling
- Headache
- Rigors; febrile convulsions and pain
- Myalgia; arthralgia; joint swelling
- Fever
- Diarrhoea & vomiting
- Lymph node swelling
- Allergic/anaphylactic reactions
- Rash, urticaria
- Guillain-Barré syndrome has been reported after vaccination containing tetanus toxoid
- Side effects of the vaccine include adverse reactions to all components
References:
- Immunisation Against Infectious Disease ("The Green Book") — Dept of Health (2004)
- Entry for Aventis Pasteur® on http://emc.medicines.org.uk/ (Sept 2004)
[REPEVAX] © Liz Bevan-Jones SRN LCH RSHom: November 2004