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VAERS Data Reveals Massive Spike in Vaccine Adverse Events—What’s Really Happening? | Serious vaccine risks accepted by FDA Serious Adverse Events https://www.fda.gov/media/186738/download?attachment MNEXSPIKE group Serious adverse events were reported by 2.7% of participants (n=156) Comparator vaccine Serious adverse events were reported by and 2.6% of participants (n=151) (median follow-up of 8.8 months). https://cardiovascular-research-and-innovation.reseaprojournals.com/archive_files/Myocard
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