In a startling revelation, Health Canada has confirmed the presence of DNA contamination in Pfizer’s COVID-19 vaccines. Even more concerning is the fact that Pfizer did not disclose this contamination to the public health authority, an admission that has been described as “epic” by some experts.
The DNA contamination includes the Simian Virus 40 (SV40) promoter and enhancer, a factor that Pfizer had not previously disclosed. This is particularly alarming as some experts suggest that this contamination poses a cancer risk due to its potential integration with the human genome.
Health Canada explained that while Pfizer provided the full DNA sequences of the plasmid in its vaccine during the initial submission, it failed to specifically identify the SV40 sequence. This is a significant lapse on Pfizer’s part, as sponsors are expected to identify any biologically functional DNA sequences within a plasmid.
This revelation came after scientists Kevin McKernan and Phillip J. Buckhaults discovered bacterial plasmid DNA in the mRNA COVID-19 vaccines, at levels potentially exceeding limits set by regulatory agencies.
Despite this alarming discovery, Health Canada maintained that the risk-benefit profile still supports the use of the Pfizer-BioNTech vaccine. However, critics argue that this statement is not credible and question why mainstream regulatory agencies and the media have remained silent on this issue.
Viral immunologist Dr. Byram Bridle emphasized the gravity of Health Canada’s admission, stating that Pfizer was obligated to disclose all bioactive sequences in the bacterial plasmid DNA used to manufacture their vaccines.
This contamination issue is not isolated; it appears to be an ongoing problem. Immunologist, biologist, and biochemist Jessica Rose, Ph.D., pointed out that residual DNA has been found not only in Pfizer and Moderna vaccines but also in older and newer vials, including the adult monovalent XBB.1.5 vaccine. This underscores the urgency of addressing this issue.
SV40, a virus frequently used in gene therapy, can potentially integrate into the human genome, leading to serious consequences. The presence of SV40 in the vaccines is a significant concern, as it could result in long-term genetic alterations with unknown implications.
Experts warn that this contamination could lead to various adverse reactions, including cancer, anaphylaxis, and other severe responses. The potential long-lasting effects of this contamination are particularly worrisome.
The preprint study by McKernan, Rose, and others also highlighted an undisclosed manufacturing change between Pfizer’s clinical trial vaccines and those distributed to the public. This raises questions about the consistency and safety of the vaccines provided to the public.
The implications of this DNA contamination are far-reaching, potentially affecting the legal liability of vaccine manufacturers. The Public Readiness and Emergency Preparedness (PREP) Act, which previously shielded vaccine manufacturers, may now face scrutiny in light of evidence of fraud and contamination.
In conclusion, the confirmation of DNA contamination in Pfizer’s COVID-19 vaccines, along with the failure to disclose this to regulatory agencies, is a matter of grave concern. It raises serious questions about the safety and integrity of the vaccination process, necessitating urgent and thorough investigation.