REVAXIS®
Available from October 2004, for children aged 14-15 years and adults when travelling.
Abbreviated vaccine composition: dT/IPV (low-dose Diphtheria and Tetanus; inactivated Polio).
Contains:
- Purified Diphtheria toxoid (2 I.U.)
- Purified Tetanus toxoid (20 I.U.)
- Inactivated Polio virus, types 1/2/3 (40, 8 and 32 Dantigen units respectively)
- Aluminium hydroxide
- 2-phenoxyethanol (phenol) - a preservative
- Medium 199 (amino acids, mineral salts, vitamins, polysorbate 80)
- Neomycin, streptomycin and polymyxin B - antibiotics
- Formaldehyde
- Polio viruses are propagated on Vero (African green monkey kidney) cells
Undesirable effects (as reported by Dept of Health and Aventis Pasteur®):
- Local injection site reactions - pain, redness, hardness & swelling
- Lymphadenopathy, vertigo, nausea & vomiting
- Fever; malaise
- Myalgia; arthralgia (joint pains); headache
- Flu-like symptoms
- Allergic/anaphylactic reactions
- Urticaria, rash, facial oedema
- 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)
[REVAXIS] © Liz Bevan-Jones SRN LCH RSHom: November 2004