Florida Surgeon General Calls for Halt in Use of COVID-19 mRNA Vaccines
Florida Surgeon General Calls for Halt in Use of COVID-19 mRNA Vaccines
“[T]hese vaccines are not appropriate for use in human beings.“
The following statement was released from the Florida Department of Health (DOH) on Tuesday:
Tallahassee, Fla. — On December 6, 2023, State Surgeon General Dr. Joseph A. Ladapo sent a letter to the United States Food and Drug Administration (FDA) Commissioner Dr. Robert M. Califf and Center for Disease Control and Prevention (CDC) Director Dr. Mandy Cohen regarding questions pertaining to the safety assessments and the discovery of billions of DNA fragments per dose of the Pfizer and Moderna COVID-19 mRNA vaccines.
The Surgeon General outlined concerns regarding nucleic acid contaminants in the approved Pfizer and Moderna COVID-19 mRNA vaccines, particularly in the presence of lipid nanoparticle complexes, and Simian Virus 40 (SV40) promoter/enhancer DNA. Lipid nanoparticles are an efficient vehicle for delivery of the mRNA in the COVID-19 vaccines into human cells and may therefore be an equally efficient vehicle for delivering contaminant DNA into human cells. The presence of SV40 promoter/enhancer DNA may also pose a unique and heightened risk of DNA integration into human cells.
In 2007, the FDA published guidance on regulatory limits for DNA vaccines in the Guidance for Industry: Considerations for Plasmid DNA Vaccines for Infectious Disease Indications (Guidance for Industry). In this Guidance for Industry, the FDA outlines important considerations for vaccines that use novel methods of delivery regarding DNA integration, specifically:
DNA integration could theoretically impact a human’s oncogenes – the genes which can transform a healthy cell into a cancerous cell.
DNA integration may result in chromosomal instability.
The Guidance for Industry discusses biodistribution of DNA vaccines and how such integration could affect unintended parts of the body including blood, heart, brain, liver, kidney, bone marrow, ovaries/testes, lung, draining lymph nodes, spleen, the site of administration and subcutis at injection site.
On December 14, 2023, the FDA provided a written response providing no evidence that DNA integration assessments have been conducted to address risks outlined by the FDA themselves in 2007. Based on the FDA’s recognition of unique risks posed by DNA integration, the efficacy of the COVID-19 mRNA vaccine’s lipid nanoparticle delivery system, and the presence of DNA fragments in these vaccines, it is essential to human health to assess the risks of contaminant DNA integration into human DNA. The FDA has provided no evidence that these risks have been assessed to ensure safety. As such, Florida State Surgeon General Dr. Joseph A. Ladapo has released the following statement:
“The FDA’s response does not provide data or evidence that the DNA integration assessments they recommended themselves have been performed. Instead, they pointed to genotoxicity studies – which are inadequate assessments for DNA integration risk. In addition, they obfuscated the difference between the SV40 promoter/enhancer and SV40 proteins, two elements that are distinct.
DNA integration poses a unique and elevated risk to human health and to the integrity of the human genome, including the risk that DNA integrated into sperm or egg gametes could be passed onto offspring of mRNA COVID-19 vaccine recipients. If the risks of DNA integration have not been assessed for mRNA COVID-19 vaccines, these vaccines are not appropriate for use in human beings.
Providers concerned about patient health risks associated with COVID-19 should prioritize patient access to non-mRNA COVID-19 vaccines and treatment. It is my hope that, in regard to COVID-19, the FDA will one day seriously consider its regulatory responsibility to protect human health, including the integrity of the human genome.”
In the spirit of transparency and scientific integrity, State Surgeon General Dr. Joseph A. Ladapo will continue to assess research surrounding these risks and provide updates to Floridians.
Why would any healthy and thinking person want to be injected with anything - especially since there wasn't any "pandemic"! Of course, that won't stop "them" from doing it again! It's actually scary; the number of people who fell for the PsyOps the first time around...how about the second time?
Since the C19 injections were granted and rolled out to the U.S. public by Emergency Use Authorization--and were driven by DoD contracts, not by HHS, FDA, CDC, nor NIH contracts--they were not required, by law, to demonstrate valid and reliable (the two benchmarks of scientific studies/research) scientific data.
And all participants involved in this C19-jab rollout (i.e., DoD, FDA, CDC, manufacturers, distribution chains, doctors, nurses, injectors, etc.) are immune from liability for any harms/damages caused by the injections. By law!
(However, I don't think this immunity to liability applies to the blatant and knowing lies that were told to us by Fauci, Walenski, etc. Those deceitful acts enabled crimes against humanity, IMO.)
The only reason Pfizer/FDA released its study data/info (much of which was redacted) is because of a FOIA lawsuit requiring them to do so; which revealed that their studies were neither valid nor reliable, which is why Pfizer/FDA tried to get those results kept from the public for 75 years!!!!!!
I'm guessing that all these knowing perpetrators, from the DoD on down, are hoping that their acts against humanity are "too big to fail," that it would take at least a decade, or more, to bring these perpetrators to justice; especially because with the $billions in revenues they've made (off the backs of taxpayers who funded it all) they can now afford to finance their power/money grabbing schemes; they're predictably going to roll out more plandemic crises that will keep us all so afraid and confused by their chaos-generating global maneuvers that the practicability of pursing justice will be functionally a moot endeavor.
God help us all.