FDA forced to release documents admitting they knew COVID vaccines caused heart inflammation.
FDA knew there were serious health issues with COVID vaccines but approved them anyway without transparency.
The documents weren't made available until a judge ordered the FDA and Pfizer to release them after a Freedom of Information Act lawsuit was filed against the FDA. Now, 800 days after the FDA approved the "Safe and effective" COVID-19 vaccines, the documents are finally available to the public for review.
Now, independent scientists and researchers can see exactly what FDA regulators saw when they made their decision to push out the COVID vaccines onto the public.
Not only were there serious safety signals with these experimental vaccines - including platelet disorders, heart inflammation and vaccine-associated enhanced disease - but there were also indications that the government regulators knew that these problems were going to be significant and the adverse event reporting systems were incapable of quantifying the issue in the population.
In the documents, the FDA indicated that they knew its own safety monitoring system was "Not sufficient" for assessing the risk of heart conditions associated with Pfizer's COVID-19 vaccines.
The FDA's adverse events surveillance system was unable to assess the risks of heart inflammation in the population, and there was plenty of evidence in the clinical studies to suggest that the vaccines would end up causing these adverse events en masse.
No comments:
Post a Comment