colinnew
The records show that Johnson & Johnson, as part of its submission to the FDA for approval of its COVID vaccine, did not include studies of the spike protein encoded in the J&J vaccine. Recently they pulled a recommendation of J&J vaccine altogether. I believe this is because this VV vaccine is de-attenuating in the body and the recipients are spreading a chimeric spike adenovirus cause hepatitis in the adenovirus-naive, which is mostly children.
Additionally, Pfizer had a distribution study on animals that proves they knew that the LNPs travel all over the body!
(Pages 3-36 of downloadable documents)
Additionally, This same Pfizer/BioNTech study notes “No genotoxicity studies are planned for BNT162b2 [the Pfizer/BioNTech COVID vaccine] as the components of the vaccine constructs are lipids and RNA and are not expected to have genotoxic potential (WHO, 2005).” Similarly, “Carcinogenicity studies with BNT162b2 have not been conducted as the components of the vaccine construct are lipids and RNA and are not expected to have carcinogenic or tumorigenic potential.”
The truth; however, is that the LNPs are allowed to distribute production of pathogenic spike throughout the body. These proteins, along with the injection itself (pseudouridine) downregulates your natural defenses and interacts with tumor signaling. Carcinogenic studies would reveal that this will eventually lead to cancer. This was an extreme regulatory fail.
JW v HHS FDA Pfizer BioNTech Vaccine prod 3 02418 – Judicial Watch
