The confidential Pfizer documents, that the U.S. Food and Drug Administration (FDA) has been forced to publish by court order, reveal that Pfizer presented evidence of Covid-19 vaccine recipients suffering auto-immune disease and Vaccine-Associated Enhanced Disease as adverse events, but the FDA chose to ignore it.
The Pfizer Covid-19 injection uses a technology that prior to the end of December 2020, had never before been authorised for use in Humans. It is known as mRNA.
And there’s a pretty good reason as to why it had never been authorised for use in Humans. During animal trials for SARS and MERS, it had the opposite of its intended effect and actually worsened disease by inducing antibody-dependent enhancement.
Eighteen months after the administration of the injections in the trials, all the animals had died.
Yet, despite this, the Pfizer jab was granted emergency-use authorisation all around the world and administered to millions.
Well apparently, it was to protect people against a disease that statistically kills less than 0.2% of those it infects, the vast majority being elderly, vulnerable and having existing underlying conditions.
But even there it has failed.