by Sen. Ron Johnson, theburningplatform.com
December 31, 2021 07:56 AM
Via Mercola
Story at-a-glance
According to Brook Jackson, a whistleblower who worked on Pfizer’s Phase 3 COVID jab trial, data were falsified, patients were unblinded, the company hired poorly trained people to administer the injections, and follow-up on reported side effects lagged way behind
The FDA did not follow up on Jackson’s complaint or investigate the allegations before granting full licensing to Pfizer’s Comirnaty shot
FDA now wants 75 years to drip out the data it relied on to grant full licensing to Comirnaty
An adverse event report from Pfizer, covering December 2020 through the end of February 2021, shows the shot causes severe and often long-term, unresolved injuries
Pfizer’s data also show the shot causes severe injuries in pregnant and nursing women. Based on these data alone, which the FDA was aware of at the end of April 2021, the Pfizer shot should have been pulled from the market