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Have you seen the document dump on the Pfizer vaccine data? It’s a bombshell. No wonder the FDA fought to keep it hidden for 55 years.
Here is the quick takeaway:
By February of 2021, Pfizer had already received more than 1,200 reports of death allegedly caused by the vaccine and tens of thousands of reported adverse events, including 23 cases of spontaneous abortions out of 270 pregnancies and more than 2,000 reports of cardiac disorders.
Bear in mind, this is Pfizer’s own data.
Click here to read the report.
This document provides an integrated analysis of the cumulative post-authorization safety data, including U.S. and foreign post-authorization adverse event reports received through 28 February 2021.
2. METHODOLOGY
Pfizer is responsible for the management post-authorization safety data on behalf of the MAH BioNTech according to the Pharmacovigilance Agreement in place. Data from BioNTech are included in the report when applicable.
Pfizer’s safety database contains cases of AEs reported spontaneously to Pfizer, cases reported by the health authorities, cases published in the medical literature, cases from Pfizer-sponsored marketing programs, non-interventional studies, and cases of serious AEs reported from clinical studies regardless of causality assessment.
The limitations of post-marketing adverse drug event reporting should be considered when interpreting these data:
Reports are submitted voluntarily, and the magnitude of underreporting is unknown. Some of the factors that may influence whether an event is reported include: length of time since marketing, market share of the drug, publicity about a drug or an AE, seriousness of the reaction, regulatory actions, awareness by health professionals and consumers of adverse drug event reporting, and litigation.
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https://www.globalresearch.ca/bombshell-document-dump-pfizer-vaccine-data/5763397
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