Under the freedom of information Act (FOIA) the FDA was ordered to release to PHMPT the Pfizer documents relied upon to make their regulatory assessment for the Pfizer COVID-19 vaccine. On 17 November 2021 a batch of documents were released and the document titled “5.3.6 postmarketing experience” in Appendix 1, from page 30, shows a list of 1295 adverse events reported following vaccination. [1, 2]
