This report outlines that the FDA knew there were 1200 deaths and 25,000 nervous system adverse events in the first two and a half months of the Pfizer vax rollout, and yet still declared the shots safe.
Not only > 42,000 events reported with known 1223 deaths, but another 11,361 Not recovered at the time of report and another 9400 unknown. That’s 21,984 out of 42,000 ( 52% )
Pg. 29: 5. SUMMARY AND CONCLUSION
Review of the available data for this cumulative PM experience, confirms a favorable
benefit: risk balance for BNT162b2. (Well, yeah, if deaths and tens of thousands reportable adverse reactions don’t count.)
Begriming on pg. 30 there are 9 pages in exceedingly small print of LIST OF ADVERSE EVENTS OF SPECIAL INTEREST. I estimate 3000 - 4000.
No wonder Pfizer was reluctant to disclose the required documents. Thanks for posting, Russell.
Here’s the actual Pzizer report in pdf form as released for the FOIR
5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT
REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021
https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf
Not only > 42,000 events reported with known 1223 deaths, but another 11,361 Not recovered at the time of report and another 9400 unknown. That’s 21,984 out of 42,000 ( 52% )
Pg. 29: 5. SUMMARY AND CONCLUSION
Review of the available data for this cumulative PM experience, confirms a favorable
benefit: risk balance for BNT162b2. (Well, yeah, if deaths and tens of thousands reportable adverse reactions don’t count.)
Begriming on pg. 30 there are 9 pages in exceedingly small print of LIST OF ADVERSE EVENTS OF SPECIAL INTEREST. I estimate 3000 - 4000.
Would you know who prepared this report?
Hi, Michael. Pfizer. I just posted Pfizer's actual report pdf link above.
thank you kindly