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The nonprofit Children’s Health Care sued the US Food and Drug Administration for withholding the results of key COVID-19 vaccine safety analyses.
Since the start of the COVID pandemic, the FDA has acted as a proxy for Big Pharma and blocked effective treatments for the virus while simultaneously approving dangerous and ineffective COVID vaccines.
The FDA lied about ivermectin and then they lied about ivermectin.
The FDA has also ignored thousands of reported deaths and tens of thousands of hospitalizations linked to experimental COVID vaccines.
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The FDA did not protect the US public. The FDA was a rubber stamp for Big Pharma.
How many Americans died and continue to die because of their negligence?
The Epoch Times reported:
The US Food and Drug Administration (FDA) has been sued to withhold the results of key COVID-19 vaccine safety analyses.
The FDA’s actions violate federal law, a new lawsuit filed Jan. 26 in federal court in Washington by the nonprofit Children’s Health Care (CHD) claims.
The suit is seeking raw results from the FDA’s analyzes of reports to the Vaccine Adverse Event Reporting System (VAERS).
A system run by the FDA with the US Centers for Disease Control and Prevention accepts reports of adverse events following vaccination.
As part of its vaccine safety monitoring, the FDA has pledged to conduct a type of analysis called Empirical Bayesian (EB) data mining on reports to see if any safety signals are triggered. The codes give agencies an idea of what problems may be caused by vaccines. Agencies must investigate the signals to verify them or determine that they are not related to vaccination.
“A report to VAERS does not mean that a vaccine caused an adverse event. But VAERS can provide important information to CDC and FDA. If it appears that a vaccine may have caused a problem, FDA and CDC will investigate further and take action if necessary,” the CDC says on its website.
The FDA denied CHD’s request for data mining results, saying the documents were “intra-agency memoranda containing opinions, recommendations, and policy discussions within the FDA’s investigative process, from which factual information cannot reasonably be distinguished.”
