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Pfizer trial whistleblower, Brook Jackson, knows of at least 10 cases of anaphylaxis in the Pfizer trial, but 0 cases were reported to the FDA. This is fraud.Steve Kirsch 18 hr ago Executive summaryWe have yet another piece of evidence suggesting Pfizer understated certain life-threatening serious adverse events by a factor of 10X or moreIntroductionI’ve written about the COVID vax clinical trial fraud before. These things never get investigated by anyone and the medical community ignores all of them without investigation. That’s the way science works I guess.But Brook Jackson just noted this:Brook was involved in the Pfizer trial. She...

VIDEO interview at link (about 22 minutes) Whistleblower [Brook Jackson] sues after discovering falsified and fabricated clinical trial data, lack of informed consent for participants, lack of staff, improper vial storage and countless other egregious abuses coming out of her trial sites that tested COVID vaccines for Pfizer. In this episode of “Good Morning CHD,” she shares more information about the lawsuit and why it is critical for us and our families.

A whistleblower lawsuit alleging fraud during Pfizer’s COVID vaccine trials is moving forward, after a district court judge unsealed the complaint, including 400 pages of exhibits. Brook Jackson in January 2021 sued Pfizer and two companies the drugmaker contracted with to work on the trials: Ventavia Research Group and ICON PLC. Jackson worked for Ventavia for a brief period in 2020 before being fired after she filed a complaint with the U.S. Food and Drug Administration (FDA) over alleged improprieties she observed during the vaccine trials. She also gave The BMJ a cache of internal company documents, photos and recordings...

London — The British Medical Journal, or The BMJ, released a report that suggests there is damning evidence that Pfizer’s clinical trials were poorly managed and data was falsified, according to a whistleblower, while the Food and Drug Administration (FDA) apparently turned a blind eye and ignored concerns addressed to them. The report was released on Tuesday, the same day the Centers for Disease Control (CDC) approved an emergency use authorization (EUA) to use the Pfizer jab on kids. Stories like this suggest the pharmaceutical companies, FDA and CDC are more concerned with protecting a cash cow than they are...