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Judicial Watch: FDA Records Show Significant Number of mRNA Test Rats Born with Skeletal Deformations

Judicial Watch announced today that it received 699 pages of records from the Department of Health and Human Services (HHS) regarding data Moderna submitted to the Food and Drug Administration (FDA) on its mRNA COVID-19 vaccine, which indicate a “statistically significant” number of rats were born with skeletal deformations after their mothers were injected with the vaccine. The documents also reveal Moderna elected not to conduct a number of standard pharmacological studies on the laboratory test animals.

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Pfizer And Moderna To Investigate Their Own Vaccines For Myocarditis Risks

Why is Big Pharma investigating their own covid vaccines for myocarditis side effects if the vaccines were already supposedly tested and proven safe and effective? Both Pfizer and Moderna have announced that they will be undertaking studies to determine the longer term risks of Myocarditis (an inflammatory condition of the heart which can lead to death) for people who have been injected with the mRNA based covid vaccines.  The decision comes after the release of multiple medical studies which show a correlation and causation between the vaccines and an exponential increase in heart problems, specifically among men 40 years old and younger.  Only a year ago the link between covid vaccinations and myocarditis was widely denied.  Studies also show that myocarditis risk increases with the number of boosters a person has taken.

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RNA for Moderna’s Omicron Booster Manufactured by CIA-Linked Company

Since late last year, messenger RNA for Moderna’s COVID-19 vaccines, including its recently reformulated Omicron booster, has been exclusively manufactured by a little known company with significant ties to US intelligence. National Resilience was founded relatively recently, in November 2020, and describes itself as “a manufacturing and technology company dedicated to broadening access to complex medicines and protecting biopharmaceutical supply chains against disruption.”  Resilience was co-founded by Biotech venture capitalist Robert Nelsen. Nelsen was one of the earliest investors in Illumina, a California-based gene-sequencing hardware and software giant that is believed to currently dominate the field of genomics. As mentioned in a previous Unlimited Hangout investigation, Illumina is closely tied to the DARPA-equivalent of the Wellcome Trust known as Wellcome Leap, which is also focused on “futuristic” and transhumanist “medicines.” Nelsen is now chairman of National Resilience’s board, which is a “Who’s Who” of big players from the US National Security State, Big Pharma and Pharma-related “philanthropy.” Another notable board member, in discussing Resilience’s intelligence ties, is Drew Oetting. Oetting works for Cerberus Capital Management, the firm headed by Steve Feinberg who previously led the President’s Intelligence Advisory Board under the Trump administration.  Cerberus is notably the parent company of DynCorp, a controversial US national security contractor tied to numerous scandals, including scandals related to sex trafficking in conflict zones. Oetting is also part of the CIA-linked Thorn NGO ostensibly focused on tackling child trafficking that was the subject of a previous Unlimited Hangout investigation. In addition to these intelligence-linked individuals, the rest of Resilience’s board includes the former CEO of the Bill & Melinda Gates Foundation, Susan Desmond-Hellmann; former FDA Commissioner and Pfizer board member, Scott Gottlieb; two former executives at Johnson & Johnson; former president and CEO of Teva Pharmaceuticals North American branch, George Barrett; CalTech professor and board member of Alphabet (i.e. Google) and Illumina, Frances Arnold; former executive at Genentech and Merck, Patrick Yang; and Resilience CEO Rahul Singhvi.

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Criminal Pharmaceutical Cartel Providing COVID-19 Injections Back in the News This Week as Their Products Harm the Public

I wonder how many people who have eagerly received COVID-19 injections from Pfizer and Johnson and Johnson are aware that these are two of the largest criminal organizations in the world? The pharmaceutical industry as a whole is the largest criminal cartel in the world, with no serious competitors. Both Pfizer and Johnson and Johnson were back in the news this week, because their products have harmed so many people. Yesterday, it was announced that Johnson and Johnson had reached a $26 BILLION settlement to end litigation over thousands of opioid lawsuits. Over the last two decades, the opioid and addiction crisis killed roughly 500,000 Americans. Today, it was announced that Pfizer was recalling its popular "stop smoking" drug Chantix, as it has been discovered to potentially cause cancer, though a spokesperson said Pfizer believed the drug's benefits "outweigh the very low potential risks." Hmm... Where have we heard that marketing gimmick before: "The drug's benefits outweigh the risk"? And they're making this claim in regards to a drug that can help you quit smoking, but may also cause cancer?? Sadly, most Americans just blindly trust these criminal pharma cartels and their products, and will keep on using them.

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Moderna Experimental mRNA Vaccine Issued Emergency Use Authorization by the FDA Illegally

After an FDA Advisory Committee voted 20 to 0 with one abstention to issue Moderna emergency use authorization (EUA) for their mRNA experimental COVID vaccine, the FDA took their advice today and issued the EUA. As is the case with the Pfizer mRNA experimental vaccine which received an EUA last week, it is important to understand that this vaccine is NOT approved by the FDA. It is only authorized to be used in emergency situations, and the Health Bureaucrats who make these decisions for everyone have already planned to make COVID an "emergency pandemic" that apparently will last for more than a year, if not longer. The Advisory Committee that met on Thursday, much like the same Advisory Committee that met last week to give the go-ahead to the Pfizer experimental mRNA COVID vaccine, is entirely comprised of pharmaceutical industry insiders, such as Paul Offit of The Children’s Hospital of Philadelphia who himself is a patent holder of a vaccine in the CDC Childhood Vaccine schedule, and Paula Annunziato, a top executive for Merck pharmaceutical company, a major producer of vaccines. The sole abstention came from Michael Kurilla, who works for the National Institute of Health. He stated: “I abstained because I am uncomfortable with the language. In the midst of a pandemic and with limited vaccine supply available, a blanket statement for individuals 18 and older is just too broad. I’m not convinced that for all of those age groups that the benefits do outweigh the risks. I want to see it more targeted toward people at high risk of serious and life-threatening COVID-19 disease.” The other concern that was allegedly discussed was the fact that three of the trial participants contracted Bell’s palsy, which causes paralysis in the face. The trial group also saw 13 deaths, 6 in the vaccine group, and 7 in the placebo group. There were only 6 deaths total in the Pfizer trials. Nevertheless, the only thing they were voting on for emergency use authorization, was whether or not the potential benefits of the vaccine out-weighed the risks, and not whether or not people were going to be injured and killed by the vaccine, as that just seems to be an acceptable side effect.

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Robert F. Kennedy, Jr. Wants Investigation on Potential Life-Threatening Anaphylaxis if Injected with Moderna’s COVID Vaccine

On August 26, Children’s Health Defense (CHD) wrote a letter to Dr. Jerry Menikoff, Director of the Department of Health and Human Services’ Office of Human Research Protection (OHRP), asking for an investigation into serious safety concerns with the COVID-19 vaccine being developed by Moderna. Moderna’s version of the vaccine, championed by Dr. Anthony Fauci and funded with $500 million in taxpayer dollars through Dr. Fauci’s National Institute of Allergy and Infectious Diseases, contains polyethylene glycol (PEG), a molecule to which approximately 72% of the American population have antibodies and 8% have highly elevated levels of antibodies.  People who have pre-existing PEG antibodies could experience life-threatening anaphylaxis if injected with PEG-containing substances such as the Moderna COVID vaccine. Additionally, antibodies to PEG can both decrease the effectiveness of the vaccine and increase the risk of side effects. CHD board chair Robert F. Kennedy, Jr. also wrote a personal letter to Dr. Fauci emphasizing that these serious safety concerns must be addressed, urging that trial participants be advised of the unique risks associated with PEG. At the time of publication, no response was received from either the OHRP or Dr. Fauci.

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