Early in the manufacturing of mRNA for COVID-19 vaccines, the companies used a slower process to make the mRNA from the DNA code of the Wuhan Spike protein.
Late in the Pfizer trials, the company switched to a fast, mass production method using E. Coli to ramp up huge production of DNA from which the mRNA could be cranked out.
Pfizer apparently used the simian DNA tumor virus SV40 (promoter and enhancer sequences) to upregulate the synthesis of the genetic code. These potentially oncogenic pieces of DNA should be dissolved with enzymes and washes in the mRNA purification process.
Apparently, the biodefense contractors making the products have manufacturing processes not up to GMP (good manufacturing practices).
The world has been very uncomfortable with the intentionally-left-blank product inserts in the vial packages and the lack of full ingredient disclosure by the companies and the US FDA. Dr. Renata Moon hammered this home at the December 7, 2022, US Senate Panel on Vaccines.
In this fast-paced, heavily referenced interview, I had Kevin McKernan, a molecular biologist, explain what he found in the Pfizer and Moderna vials. I pressed him on cDNA, what it means, and SV40. He emphasized and cited multiple other investigators worldwide who have found the same contaminants. These findings alone should prompt a worldwide recall and investigation into product safety and purity.
McKernan testified at the June 15, 2023, FDA Vaccines and Related Biological Products Advisory Committee meeting to get this discovery of contaminated vials on the record. He believes his concerns fell on deaf ears. The caveats of his work are that only two vials of BA3/BA4 bivalent Pfizer from the same lot were examined.
Of note, cDNA but not SV40 code was found in two vials of Moderna. Listen to this issue of the McCullough Report, and you will decide if we have something to worry about with this development.
So let’s get real, let’s get loud; on America Out Loud Talk Radio, this is The McCullough Report!
Dr. McCullough is an internist, cardiologist, and epidemiologist managing the cardiovascular complications of both the viral infection and the injuries developing after the COVID-19 vaccine in Dallas, TX, USA. Since the outset of the pandemic, Dr. McCullough has been a leader in the medical response to the COVID-19 disaster and has published “Pathophysiological Basis and Rationale for Early Outpatient Treatment of SARS-CoV-2 (COVID-19) Infection,” the first synthesis of sequenced multidrug treatment of ambulatory patients infected with SARS-CoV-2 in the American Journal of Medicine and subsequently updated in Reviews in Cardiovascular Medicine. He has dozens of peer-reviewed publications on the infection and has extensively commented on the medical response to the COVID-19 crisis in TheHill, America Out Loud, NewsMax, One America News, Victory Channel, NTD, and FOX NEWS Channel. Dr. McCullough has testified on pandemic response multiple times in the US Senate, Texas Senate Committee on Health and Human Services, Arizona Senate, Colorado General Assembly, New Hampshire Senate, Pennsylvania Senate, and South Carolina Senate. On December 7, 2022, Dr. McCullough co-moderated a Senate Panel and concluded that all COVID-19 vaccines should be removed from the market for excess mortality. Dr. McCullough has reviewed thousands of reports, participated in scientific congresses, group discussions, and press releases, and has been considered among the world’s top experts on COVID-19. The McCullough Report: Sat | Sun 2 PM ET – Internationally recognized Dr. Peter A. McCullough, known for his iconic views on the state of medical truth in America and around the globe, pierces through the thin veil of mainstream media stories that skirt the significant issues and provide no tractable basis for durable insight. Listen on iHeart Radio, our world-class media player, or our free apps on Apple, Android, or Alexa. Each episode goes to major podcast networks early in the week and can be heard on-demand anywhere in the world.
