- Ruth Lopert, principal medical adviser1,
- Terry Nolan, head2
- 1Therapeutic Goods Administration, Symonston, ACT 2609, Australia
- 2Melbourne School of Population Health, University of Melbourne and Murdoch Children’s Research Institute, Parkville, VIC 3010, Australia
- ruth.lopert{at}tga.gov.au
Collignon and colleagues assert that febrile reactions seen in pandemic influenza A/H1N1 vaccine (Panvax) clinical trials were an overlooked predictor of the excess febrile reactions seen with CSL’s seasonal trivalent influenza vaccine that prompted suspension of its use in children under 5.1 Yet most febrile reactions reported in the Australian Panvax trial were mild, with severe fever (>39.5°C) in only 2%.2 Fever …
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