FYI: buried at the very end of the 54-page Moderna COVID-19 vaccine Emergency Use Authorization briefing document is an important disclosure of a Serious Adverse Event that befell a vaccinated individual.
- As of December 6, 2020, there were 3 SAEs reported in the vaccine group: a 65-year-old participant with community acquired pneumonia 25 days after vaccination, a 72-year-old participant with arrhythmia after being struck by lightning 28 days after vaccination, and an 87-year-old participant with worsening of chronic bradycardia 45 days after vaccination. On FDA review of the narratives, none of these SAEs are assessed as related.
In addition, over 90% of those vaccinated reported pain at the injection site, and three vaccine recipients died during the study (as did four placebo recipients).
Be careful out there.