Thousands Of Adverse Events since Pfizer mRNA Vaccine Rollout
Cancer Expert Dr. Chris Flowers and Spokesperson Amy Kelly are Available for Interview
Pfizer’s COVID-19 mRNA “Vaccine” Trial Data Shows instances of 73 unique types of cancers in one of their documents.
Quote from Dr. Chris Flowers:
“Very little research has been done on the harms of Lipid Nanoparticles of which some of the ingredients in them are known carcinogens.”
Amy Kelly is the Program Director for the War Room/DailyClout Pfizer Documents Analysis Project. She oversees the approximately 3,250 volunteers who are reviewing, analyzing, and reporting on the court-ordered, FDA-released Pfizer documents, as well as overseeing the approximately 350 volunteer attorneys who are identifying legal actions to be taken based on findings from the Pfizer documents. Additionally, she does research and provides answers to the public’s questions about adverse events found in the documents.
Dr. Chris Flowers, Associate Professor of Radiology (retired), University of South Florida. Previously Associate Professor of Radiology and Biomedical Imaging at the University of California, San Francisco. Retired academic cancer radiologist, author, and scientific paper reviewer for multiple radiology journals.
The analysis in Pfizer’s post-marketing document was completed on February 28, 2021. Its appendix shows 1290 Adverse Events of Special Interest (AESIs). An “adverse event” is also known as a “side effect.” Additionally, within just two and a half months after its COVID-19 vaccine received Emergency Use Authorization (EUA) approval, Pfizer documented:
- Almost 26,000 nervous system adverse events
- 17,283 musculoskeletal and connective tissue disorders
- 8,848 respiratory, thoracic and other chest and heart disorders
- 14,096 gastrointestinal disorders
Therefore, Pfizer was aware of tens of thousands of adverse events, many severe, from its mRNA COVID vaccine by the end of February 2021.
Pfizer submitted its post-marketing analysis to the U.S. Food and Drug Administration (FDA) on April 1, 2021. So, four and a half months after granting Pfizer’s vaccine EUA, the FDA knew about the tens of thousands of adverse events.
Yet, rather than informing the public and pausing the use of this drug to do further studies, both Pfizer and the FDA remained silent about the incredible harms resulting from it. Moreover, they – along with the Centers for Disease Control and Prevention (CDC), public health agencies, governments, media, and the majority of medical professionals – continued to aggressively push, and even mandate, for people to receive this harmful shot.
The data in this video is from Pfizer’s “post marketing” document, which is titled, “5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021