ATIP: What HC did about Pfizer's reported serious adverse reactions, including deaths

COMING SOON

Here was the ATIP request:

Please provide the 3 safety reports provided to HC by the manufacturer and HC’s review/reports related to all three. For each, please include

i) the date each manufacturer report was received;

ii) the date when each review was completed and by whom including expertise/specialty;

iii) findings including:

a) identified risks of the vaccine;

b) potential risks of the vaccine;

c) missing information at the writing of this report and what HC asked of the sponsor

and/or plans by HC to fill in those gaps;

d) the conclusions made by HC regarding the safety and efficacy of the Pfizer vaccine after reading the report; and

e) the method by which the 1,291 Adverse Events of Special Interest noted in the Appendix of the CUMULATIVE ANALYSIS OF POSTAUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021 document were specifically monitored by Health Canada and/or PHAC or any other federal or P/T health agency. This would include any internal or external communications such as reports, emails, briefs, text messages, records of telephone conversations, memorandums, drafts, documents, press releases and presentations in relation to same.

LINK: <https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketingexperience.pdf>