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SILVER SPRING, Maryland (LifeSiteNews) – The FDA has quietly released a statement stating that 21 people died during Pfizer’s COVID-19 vaccine clinical trial, significantly more than the company publicly reported. 

On November 8, the Food and Drug Administration (FDA) released a 30-page statement entitled “Summary Basis for Regulatory Action” to explain the rationale behind approving the Pfizer COVID-19 so-called vaccine. The report stated that 21 people in the vaccine recipient group died between November 2020 and March 2021, but the pharmaceutical company told the public in July that only 15 people had died during that period.  

“Pfizer said publicly in July it had found 15 deaths among vaccine recipients by mid-March. But it told the FDA there were 21 – at the same data cutoff end date, March 13,” wrote Alex Berenson, a former New York Times reporter and bestselling author, in his analysis of the latest information.  

“Could the discrepancy result from some odd data lag? Maybe, but the FDA briefing book also contains the number of Covid cases that Pfizer found in vaccine recipients in the trial. Those figures are EXACTLY the same as those Pfizer posted publicly in July. Yet the death counts were different,” he added.  

“Pfizer somehow miscounted – or publicly misreported, or both – the number of deaths in one of the most important clinical trials in the history of medicine.” 

To make matters worse for the FDA’s safety claims, with 21 deaths in the group of 22,000 who received the shot, and only 17 deaths in the placebo group of 22,000 who received a benign saline shot instead, the new data shows that those who received Pfizer’s treatment died in greater numbers than those who did not. Nevertheless, the experimental injections were still approved for widespread use. 

Due to the discrepancy between Pfizer’s public data and the data they sent to the FDA, the cause of death following the jab is only known for 15 of the 21 subjects who died. Of the 15 post-shot deaths with a known cause, 6 of the fatalities involved cardiac-related events. For the unvaccinated placebo group, only 2 people died from cardiac-related events.  

“Were the extra [6] deaths cardiac-related? It is impossible to know,” Berenson stated.  

“The FDA did not report any additional details of the deaths, saying only that none ‘were considered related to vaccination,’” he continued.  

“But with tens of thousands of post-vaccine deaths now reported in the United States and Europe – and overall non-Covid death rates now running well above normal in many countries – a fresh look at that vague reassurance cannot happen soon enough.” 

Bolstering Berenson’s argument, data from the World Health Organization, the European Union, and America’s Vaccine Adverse Event Reporting System (VAERS) show reports of millions of injuries and tens of thousands of deaths connected to the shots, which is more than all other vaccines combined since 1990. 

Meanwhile, the list of FDA-recognized adverse events has grown from severe anaphylactic reactions to include fatal thrombotic events, the inflammatory heart condition myocarditis (primarily in young males), and neurologically disabling diseases like Guillain Barré Syndrome. 

Further increasing the cause for concern, recent official data out of England and Wales reported a whopping 37 percent increase in non-COVID related deaths over the past 18 months, with a staggering 30 percent increase in unexplained deaths in 15–19-year-old boys.  

Regardless of the so-called “approval” from the FDA, all currently available COVID-19 vaccines are experimental, with clinical trials not set for completion until 2023.  

Despite a group of doctors and academics filing a lawsuit to obtain the FDA’s complete data profile of the Pfizer jab, the agency suspiciously denied the request for transparency and asked a judge to delay the release of the data until the year 2076, some 55 years after the FDA gave the green light to roll out the experimental shots to millions of people in the country. 

“It is difficult to imagine a greater need for transparency than immediate disclosure of the documents relied upon by the FDA to license a product that is now being mandated to over 100 million Americans under penalty of losing their careers, their income, their military service status, and far worse,” the plaintiffs’ lawyer, Aaron Siri, wrote in their suit 

“The FDA’s promise of transparency is, to put it mildly, a pile of illusions,” Siri wrote in a statement on Substack. 

“Who does the government work for?”  

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