Recently, a report has been circulating on social media following a request by multinational Pfizer for a safety evaluation of their vaccine by the regulatory authority FDA.
The report has the following title:
‘5.3.6. Cumulative analysis of post-authorization adverse event reports of PF-07302048 (BNT162B2) received through 28-feb-2021’.
You can download the document here: (At page 30 you will find all the “side” effects)
https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf
