Criminal FDA Hides Records From Moderna “Vaccine” Approval and Fabricates Data To Justify Approval For Injecting Babies With mRNA Bioweapon
FDA Sued Over Hiding Records From Moderna COVID-19 Vaccine Approval. FDA's Vaccines and Related Biological Products Advisory Committee report June 14-15 "raises serious questions of malfeasance"
Exposing The Darkness is a reader-supported publication. To support my work, please consider becoming a paid subscriber.
The criminal saga of the murderous Big Pharma and corrupt regulatory agencies continues.
The FDA is being sued by a Texas-based non-profit for refusing to comply with the Freedom of Information Act.
The National Pulse reports:
Defending the Republic, a Texas-based non-profit filed a Freedom of Information Act lawsuit against the Food and Drug Administration for refusing to turn over records related to the approval of Moderna’s COVID-19 vaccines.
The group filed a Freedom of Information Act (FOIA) request seeking the production of records relating to the Food and Drug Administration’s (FDA) internal review process of Moderna’s COVID-19 vaccine marketed as “Spikevax.” Given that the forces impacting the FDA’s decision to authorize the vaccine could have influenced Americans’ decision on whether or not to get vaccinated against COVID-19, Defending the Republic requested expedited processing of relevant records.
“Please provide all data and information submitted by Moderna relating to the FDA review and approval of Spikevax. This includes, but is not limited to, all safety and effectiveness data and information; all data and information in the biological product file; and all ingredients,” outlined the initial FOIA request.
On February 9th, less than a week after the initial FOIA was filed, the FDA refused the request for expedited processing, prompting Defending the Republic to appeal the decision.
“The FDA declined the appeal, leaving Defending the Republic with no choice but to file this action seeking a court order requiring the FDA produce the requested records on an expedited schedule— just as those who obtained a court order for the expedited production of records relating to the FDA approved Pfizer-BioNTech vaccine,” explains a complaint filed by Defending the Republic.
Defending the Republic was especially interested in better understanding the review process for Moderna’s COVID-19 vaccine, as data has shown its risk were not adequately explained to those receiving it and data surrounding its efficacy remains obscured. As Defending the Republic explains:
The lawsuit comes amidst several National Pulse exposés revealing how lobbyists from pharmaceutical companies including Moderna have entrenched themselves within Washington, D.C.
FDA Caught Creating and Using Unreliable and Inconsistent Data to Create An Illusion of COVID-19 Vaccine Efficacy as They Attempt to Justify Approval for Use in Infants and Toddlers
Urgent Action Item Below.
As promised, the FDA has ginned up a report that ostensibly will be used to try to justify “approval” (whatever they mean by that now) of COVID-19 vaccines for infants and toddlers (children < 5 years old). Here’s the report for your reference.
This report comes after a torrent of massive reports from Moderna and Pfizer that claim to review studies of the safety and efficacy of COVID-19 vaccines in children. It is not hard to see what shenanigans the FDA has been up to to try to bolster a vaccine that fewer and fewer adults want. It’s more of the same: exaggerate the apparent risk of the virus and minimizing the perception of risk. In other words, lies.
Key document: FDA's Vaccines and Related Biological Products Advisory Committee report June 14-15, 2022; this report raises serious questions of malfeasance and pure ineptness by these malfeasants
Sacrificing Children to Moloch: NHS Added mRNA Jabs to the List of Scheduled Vaccines for Children. Shots for Kids Under 5 Could Begin on June 21
Dr. Michael Yeadon: THIS MUST STOP! Pfizer Documents Show FDA Knew of Death Risk
mRNA "Vaccines" Are Gene Therapy. May cause Undesirable Side Effects That Could Delay Or Prevent Their Regulatory Approval According To BioNTech SEC Filing
Moderna SEC Filing: We May Be Delayed or Prevented From Receiving Full Regulatory approval. Unexpected Safety Issues Could Significantly Damage Our Reputation and That of Our mRNA Platform
BioNTech 2022 SEC Filing: We May Not Be Able To Demonstrate Sufficient Efficacy or Safety of Our COVID-19 Vaccine. Significant Adverse Events Could Delay or Prevent Regulatory Approval
There were 38,000,000 flu cases the winter of 2019-2020.
There were only 1,800 flu cases the winter of 2020-2021.
That’s because hospitals got paid $13,000 for every Fauci/China biological warfare virus diagnosis, and $39,000 for every biological warfare virus patient they slapped on a ventilator to kill them.
Covid is a LIE........ALL OF IT!!!!