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Between Dec. 14 and April 23, there were 3,544 deaths reported to the CDC’s Vaccine Adverse Event Reporting System [VAERS], along with 12,619 serious injuries.
One might expect these numbers would trigger an exhaustive investigation from the U.S. Food and Drug Administration. But the opposite has occurred. According to McCullough, the government has taken what amounts to a passing glance at the alarming numbers and dismissed them with a bare minimum of scrutiny.
“A typical new drug at about five deaths, unexplained deaths, we get a black-box warning, your listeners would see it on TV, saying it may cause death,” McCullough said. “And then at about 50 deaths it’s pulled off the market.”
The U.S. has a precedent for this. In 1976 during the Swine Flu pandemic the U.S. attempted to vaccinate 55 million Americans, but at that point the shot caused about 500 cases of paralysis and 25 deaths.
“The program was killed, at 25 deaths,” McCullough said.
Compare that type of response to the government’s reaction to much higher reported death numbers related to the Moderna and Pfizer shots and the contrast is alarming, McCullough said, especially when the shots have not even been granted full FDA approval and are only being allowed on the market under an Emergency Use Authorization.
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