Dr. Robert Malone: Inflammatory and toxic reactions associated with lipid nanoparticles

"We have the artifactual evidence of what was known in the form of the Pfizer common technical document that was first obtained by Byram Bridle from the Japanese it was prevented from being distributed by the US FDA and it revealed extensive understanding that we had this widespread biodistribution of these products that they caused the encoded protein to be manufactured in virtually every major tissue throughout the body."

"It was known that there was a strong inflammatory and toxic reactions associated with these lipid nanoparticles. This is fundamental knowledge. It was in the field of these cationic-based lipid nanoparticle delivery systems. It was known that these particles will deliver both RNA and DNA into cells and tissues. It was known that the modification, the pseudo-uridine, altered the immune response to the RNA. That's the whole reason why the incorporation of pseudo-uridine was performed."

"It was known that the pseudo-uridine would increase the longevity of these products, that this was not natural RNA. It was not known and not investigated as to whether or not these products would be quote shed. It was not known and not investigated whether or not these products would cause reproductive toxicity, whether they would be secreted in body fluids. A number of things that should have been investigated under normal FDA protocols and procedures not the least of which is characterization of the contamination or adulteration of the short DNA fragments, which are intrinsic to the manufacturing process, and which in prior FDA regulations have always been considered to be a risk for a form of genotoxicity called insertional mutagenesis."