How the FDA Rigs Vaccine Trial Results
Larry A. Law
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...
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.
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.
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.
I am sure you probably know this already but 2 of your links in this article take you to a page saying basically, this page may be taking your personal information. It is not secured. So I guess “they” have gotten into your site like many others. However the FDA meeting link is no problem?? Shame, shame on them all. Thanks for all your research and information.
11/15/2022 12:47:17 pm
Yes thanks Joan…we have heard from many people that this is happening when they try to go to the website or listen to a podcast or whatever. It is frustrating for sure! We have our IT working on it. HOPEFULLY it will be resolved today! Apparently it isn’t a hacker but something to do with the organization that manages our non-profit. We have to do something with a certificate so this doesn’t show up—not sure I’m understanding it exactly but we’re hearing from them that it will be resolved soon!! Thanks for the alert though as it was supposed to be fixed yesterday. 😕
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