We reveal that reports on the BNT162b2 mRNA vaccine clinical trial done in public forums by Pfizer/BioNTechand their representatives were flawed and included serious reporting errors that obscured the actual trial results. As a result, a 3.7-fold increase in cardiac events in subjects who received the BNT162b2 vaccine versus the placebo group was not reported to the public at the time of the vaccine rollout.

Pfizer-BioNTech delayed reporting vaccine-associated deaths among BNT162b2 clinical trial participants until after the U.S. Food and Drug Administration (FDA) issued an Emergency Use Authorization (EUA) for the product.

The vaccine makers also failed to account for a large number of subjects who dropped out of the trial.

The authors of the paper described it as a “forensic analysis,” defined by the U.S. National Institute for Standards and Technology as “the use of scientific methods or expertise to investigate crimes or examine evidence that might be presented in a court of law.”

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