In April 2011, following an increase in the notification of adverse events following revaccination of adults with Pneumovax 23®, the Therapeutic Goods Administration recommended that revaccination with Pneumovax 23® should not occur pending the outcome of further investigation and a review of previous advice on its use by the Australian Technical Advisory Group on Immunisation (ATAGI).
The outcome of this investigation has led to the formulation of new advice on the safety, efficacy and effectiveness of Pneumovax 23® and its place within the National Immunisation Program.
Following the review, ATAGI’s revised revaccination recommendations are:
For further information and detailed ATAGI advice, please see the Pneumococcal information, Immunisation of adults, 23 December 2011 at: http://immunise.health.gov.au/
