Keywords: Australia, TGA, Sanofi Pasteur, Panvax, H1N1, influenza, Side effects

654 suspected adverse reactions to Panvax reported to Australia’s TGA in one month

Article | 24 November 2009

The Australian national immunization program with the H1N1 2009 influenza vaccine Panvax, made by French drug major Sanofi-Aventis’ Sanofi-Pasteur unit, began on September 30, 2009, and the country’s Therapeutic Goods Administration has been closely monitoring any side effects from the use of the vaccine.

As at October 29, a total of 654 suspected side effects have been reported to the TGA following vaccination with Panvax in Australia, with over 3.75 million doses of the vaccine distributed in the country. Enjoying this article? To continue reading you need to login, take a FREE trial or subscribe.

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