How the FDA Rigs Vaccine Trial Results

Larry A. Law

The Food and Drug Administration (FDA) adopted a "Future Framework" scheme which will allow Pfizer and Moderna to reformulate, release, and sell updated COVID shots without sponsoring any more clinical safety trials. This means that untested, new COVID experimental shots will be manufactured and injected into an unsuspecting public as if they were guinea pigs. This will surely guarantee that future COVID shots will be even less effective and at the same time more lethal than previous ones. Adding more mRNA vaccines to cover more variants will result in higher adverse event rates. 

FDA Captured By Big Pharma

Toby Rogers, Ph.D. is a political economist who focuses on how Big Pharma has captured government regulatory agencies like the FDA. He explains how the FDA sneaked through the most blatant rule change in history ("Future Framework"): 

"Yesterday [June 28], the FDA's Vaccines and Related Biological Products Advisory Committee (VRBPAC) approved a bivalent COVID-19 shot with the Wuhan strain and the Omicron variant... At the meeting, the manufacturers (Moderna, Pfizer, and Novavax) were asked what their production timelines are... and they said out loud, 'So long as we don't have to provide any clinical data, we'll have them ready by fall.' No one had a problem with that...

​Wait, hold up, I thought the FDA was voting on the Future Framework yesterday? The policy question was whether reformulated COVID-19 shots would be treated as new molecular entities (which they are) in which case they should be subject to formal review or whether reformulated shots would be treated as 'biologically similar' to existing COVID-19 shots and be allowed to skip clinical trials altogether.

Apparently the FDA did not have the votes to just pass this as a policy question. If you ask anyone whether reformulated mRNA represents a new molecular entity, well of course it is, so that would require formal regulatory review. What the FDA did instead was to smuggle the policy question in disguised as a vote about reformulated 'boosters' for the fall. In essence, the FDA just started doing the Future Framework (picking variants willy nilly, skipping clinical trials) and essentially dared the committee members to turn down a booster dose--knowing that all of the VRBPAC members are hand-picked because they've never met a vaccine they did not like. So of course only two people on the committee had the courage to turn down a booster dose--even though it was based on this preposterous process (that was never formally adopted) where there was literally no data at all... By stealth, the FDA replaced a system based on evidence with a system based entirely on belief."

Worst Idea in the History of Public Health

A decision to release reformulated mRNA injections without any additional clinical safety trials has radically changed medical science for the foreseeable future. Big Pharma will have no risk associated with creating untested COVID shots. Adverse events will never show up in any safety trial. The shots will just go straight into the arms of trusting people. The manufacturer cannot be sued for any adverse outcome, so there is no check and balance on them at all. The FDA has removed all standards of protection. Clearly, they don't work for the American people but have become a rubber-stamp clearing-house for Big Pharma.   

Two Options

Most people are unaware that SARS-CoV-2 mutates 2 to 10 times faster than the influenza (flu) virus. These mutations reduce vaccine effectiveness considerably. This is what we have seen with COVID-19. In addition, when you vaccinate against a rapidly mutating virus you run the risk of pressuring it into a more virulent or vaccine-resistant form. When the VRBPAC met on April 6, 2022, all of the committee members agreed that COVID-19 shots were not working, that boosting multiple times a year was not feasible, and that the shots should be reformulated. They could have voted to withdraw the COVID shots and focus on therapeutics. But that would be a political disaster, so they are doubling down on a failed strategy of vaccine reformulation and need the cover-up of no clinical trials so as not to highlight expected adverse events. The more mRNA they put into the shot to cover all of the variants, the higher the adverse event rate will be. If they decide to include less mRNA per variant in order to keep the total amount of mRNA at current levels (100 mcg for Moderna and 30 mcg for Pfizer), then the effectiveness against any particular variant will be reduced. Either way they go, this FDA vaccine approach is 100% doomed to failure. 

Fudging Effectiveness

The FDA also insists that, due to time constraints, evaluation of effectiveness must rely on "measures other than actual health outcomes." In other words, whether the shots actually lower your risk of severe illness, hospitalization and death will have no bearing. The only measure that will be taken into account is whether or not the shot triggers a rise in antibody levels. By the way, this has never been proven to offer any significant protection. The problem with this measure is that if antibody levels are extremely high, the death rate could be extremely high too. There is so much we don't know about the virus, the shots, and the interaction between them. Allowing vaccine makers to reformulate the shots without clinical trials is a recipe for disaster. 

Vaccine Trials Are Routinely Rigged

Over the years, vaccine trials have been rigged to justify safety and efficacy. Failure to record vaccine injuries and ignoring their significance is a common tactic Big Pharma uses to make the vaccine appear safer than it is. Another common strategy is to exlude participants who are injured. 3,000 of the 4,526  children (age 6 months to 4 years) who were enrolled in Pfizer's pediatric COVID trial were excluded. That should have been a huge red flag pointing to serious, harmful, side effects. "Pfizer, one of the most criminally fined drug companies in the world, wants to weaken the laws that hold them accountable," said attorney Robert Barnes. Barnes is representing whistleblower Brook Jackson who alleges fraud in Pfizer's COVID-19 clinical trials. Pfizer is pleading not guilty and justifying their actions because the U.S. government knew about their wrongdoings but continued to do business with them. How corrupt is that? 

My wonderful mother-in-law, Nyla, sent me a short video that I am passing on to you. In the video, Dr. Scott Youngblood testifies in an outstanding, 12-minute presentation, recorded in front of the San Diego, California city council meeting on Sep 13, 2022. The city council was considering whether to continue the state of health emergency still in effect in their city and he gives a powerful summary of the problems associated with the COVID vaccination program.

On another note, Turtles All The Way Down is a must-read book. Every parent should know the difference between vaccine science and vaccine myth before deciding how to proceed with childhood vaccinations. This book is easy to read but so helpful in understanding the truth about all childhood vaccines.​