SWINE FLU ADVERSE REACTION "PRIORITY" REPORTING

With an apparent pandemic of swine flu, the Medicines and Healthcare products Regulatory Agency [MHRA] have issued a letter to Healthcare professionals with regard to reporting of any adverse reactions to the vaccines, Tamiflu [Roche] and Relenza [GlaxoSmithKline].

The letter, which can be downloaded here, announces the 'special' web-based portal, which the MHRA have named, 'The Swine Flu ADR Portal.'

Two ways of looking at this:

1, The MHRA expect a large number of reports because the vaccines will be widely used

or

2, The MHRA have their suspicions about these vaccines so want to keep a close eye on the adverse reactions.

Now call me a cynic...

Fid

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'THE EVIDENCE, HOWEVER, IS CLEAR...THE SEROXAT SCANDAL' By Bob Fiddaman
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