Eminent COVID-19 expert and highly published physician Dr. Peter McCullough provided a comprehensive well-documented presentation to colleagues regarding the “unbelievable atrocity” occurring in the West due to gene-transfer vaccine campaigns, the necessity for an “unbreakable resistance” against children receiving the jab, and the “astounding … ineptitude and willful misconduct” of public health agencies.
McCullough, who has made the case that no one in the world has more authority on this topic than him, provided detailed analysis of multiple scientific studies and data reports demonstrating the “failure of the vaccine program,” the suppression of effective early treatments, and the “robust, complete and durable” qualities of natural immunity.
Dr. Robert Malone, the architect of the mRNA platform used by the Pfizer and Moderna vaccines, and organizing co-signer of a recent public declaration in defense of early treatments, promoted the presentation, tweeting, “I’ll say it again. Watch the speech from Dr. Peter McCullough. He is on fire. And he is spot on. He [sic] summary of the data are [sic] precise and detailed. Please take the time to watch that video. And get outraged.”
Among many topics addressed by McCullough at the October 2 annual meeting of the American Association of Physicians and Surgeons was an initial focus on the serious lack of transparency of safety data and proper monitoring of the program.
“I have chaired data safety monitoring boards for over two dozen therapeutic products,” McCullough told his audience. His participation in this capacity has included heading boards for the National Institutes of Health (NIH) and Big Pharma corporations.
Data Safety Monitoring Boards (DSMB) are defined as a “ committee of clinical research experts … who monitor the progress of a clinical trial and review safety and effectiveness data while the trial is ongoing. This committee is independent of the people, organizations, and institutions conducting the clinical trial … [and] can recommend that a trial be stopped early because of concerns about participant safety …”
“I have made some critical calls as a chairman of a data safety monitoring board to shut down a program when it wasn’t safe,” McCullough explained. “And, I can tell you, that threshold is a few cases where we can’t explain it, a few cases. We get to five unexplained cases [and] we start to get very, very uncomfortable.” When “we get to 50 unexplained deaths in a release of a product, it’s gone. It’s gone. We shut it down and we figure out what went wrong. For new biologic products demand safety, safety, safety.”
1976 Swine flu vaccination campaign stopped after 25 death reports
He went on to discuss the 1976 swine flu vaccine campaign the government suspended after just 10 weeks due to 25 sudden deaths and 550 reports of Guillain-Barré syndrome following vaccination.
“The comfort level was gone. We had vaccinated 25% of our 220 million people in the United States [at the time]. And that was it! The concern for safety was too great. Deaths escalated after stopping the program up to 53. This was the standard, and still should be the standard today,” explained the editor of two medical journals.
In contrast, with our current COVID-19 gene-transfer vaccination campaign, “we are far beyond that,” McCullough said. In fact, the current death numbers are 652 times higher than they were in 1976 when the government shut down the swine flu vaccination program.
The most recent data from the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) released October 8 reports 778,683 adverse events in the U.S. following COVID vaccination, including 16,310 reports of deaths and 75,605 reports of hospitalizations, between December 14, 2020, and October 1.
In addition, it remains a concern that these figures are just “the tip of the iceberg,” as a “2010 Harvard-executed study commissioned by the Department of Health and Human Services (HHS) revealed that reported vaccine injuries to VAERS represent an estimated 1% of actual injuries.
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