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What happens after VAERS receives a report of an adverse event following vaccination with the 2009 H1N1 vaccine?

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What happens after VAERS receives a report of an adverse event following vaccination with the 2009 H1N1 vaccine?

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CDC and FDA take every adverse event report seriously. For all reports of serious adverse events, VAERS staff collects follow-up records on each case and medical officers review them closely to determine if any additional action or studies are needed.

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