Omicron Variant Sends Vaccine Makers’ Stocks Soaring, as VAERS Data Show 913,000 Reported Adverse Events After COVID Vaccines

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The Centers for Disease Control and Prevention released new data late Monday showing a total of 913,268 adverse events following COVID vaccines were reported between Dec. 14, 2020, and Nov. 19, 2021, to the Vaccine Adverse Event Reporting System (VAERS). VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.

The data included a total of 19,249 reports of deaths — an increase of 396 over the previous week — and 143,395 reports of serious injuries, including deaths, during the same time period — up 4,269 compared with the previous week.

Excluding “foreign reports” to VAERS, 664,745 adverse events, including 8,898 deaths and 56,297 serious injuries, were reported in the U.S. between Dec. 14, 2020, and Nov. 19, 2021.


Foreign reports are reports received by U.S. manufacturers from their foreign subsidiaries. Under U.S. Food and Drug Administration regulations, if a manufacturer is notified of a foreign case report that describes an event that is both serious and does not appear on the product’s labeling, the manufacturer is required to submit the report to VAERS.

Of the 8,898 U.S. deaths reported as of Nov. 19, 20% occurred within 24 hours of vaccination, 26% occurred within 48 hours of vaccination and 56% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated.

In the U.S., 447.7 million COVID vaccine doses had been administered as of Nov. 19. This includes 260 million doses of Pfizer, 171 million doses of Moderna, and 16 million doses of Johnson & Johnson (J&J).

From the 11/19/21 release of VAERS data

Every Friday, VAERS publishes vaccine injury reports received as of a specified date. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed. Historically, VAERS has been shown to report only 1% of actual vaccine adverse events.

U.S. VAERS data from Dec. 14, 2020, to Nov. 19, 2021, for 5- to 11-year-olds show:

  • 1,103 adverse events have been reported in the 5 to 11 age group since Nov. 1.
  • The rest of the reports in VAERS for children in the 5 to 11 age group occurred prior to the authorization of Pfizer’s COVID vaccine, and are due to ”product administered to the patient of inappropriate age.”

U.S. VAERS data from Dec. 14, 2020, to Nov. 19, 2021, for 12- to 17-year-olds show:


The most recent death involves a 16-year-old girl from Georgia (VAERS I.D. 1865389) who died reportedly from a heart condition and multi-organ failure two days after receiving Pfizer’s COVID vaccine.

Other recent deaths include a 16-year-old girl from Missouri (VAERS I.D. 1823671) who died after receiving her second dose of Pfizer and a 17-year-old female from Washington (VAERS I.D. 1828901) who died Oct. 29 reportedly from a heart condition after receiving her second dose of Pfizer.

  • 59 reports of anaphylaxis among 12- to 17-year-olds where the reaction was life-threatening, required treatment, or resulted in death — with 96% of cases
    attributed to Pfizer’s vaccine.
  • 560 reports of myocarditis and pericarditis (heart inflammation) with 549 cases attributed to Pfizer’s vaccine.
  • 139 reports of blood clotting disorders, with all cases attributed to Pfizer.

U.S. VAERS data from Dec. 14, 2020, to Nov. 12, 2021, for all age groups combined, show:

Man with natural immunity forced to get vaccinated against COVID to remain on the lung transplant list dies after the second dose of Moderna

Bobby Bolin, a 49-year-old Texas man who previously had COVID, was told he would have to get vaccinated against COVID in order to be eligible for a double-lung transplant, even though he had already recovered from the virus.

After his second Moderna shot, received on April 17, Bolin developed a pulmonary embolism and atrial fibrillation — a heart condition characterized by an irregular heartbeat, shortness of breath, chest pain, and extreme fatigue. His health rapidly deteriorated and he passed away Aug. 20, before receiving new lungs.

In an exclusive interview with The Defender, his wife, Amy Bolin, said there was no reason her husband should have been forced to get the vaccine in order to receive new lungs, but unfortunately, he was desperate and very sick.

Amy said she didn’t know what timeline her husband had with his organs, but she saw a complete change in him over four months’ time and doesn’t want others to face the same things they experienced.

Pfizer, Moderna vaccines ‘dramatically increase’ heart attack risk

In an analysis presented during a meeting of the American Heart Association, Dr. Steven Gundry, a pioneer in infant heart transplant surgery, said mRNA COVID vaccines put many patients at higher risk of a new acute coronary syndrome, such as a heart attack.

The analysis concluded in part that mRNA vaccines “dramatically increase inflammation on the endothelium and T cell infiltration of cardiac muscle and may account for the observations of increased thrombosis, cardiomyopathy and other vascular events following vaccination.”

Thousands of heart-related injuries have been reported following COVID mRNA vaccines, and scientists have established a myriad of heart- and blood-related effects in some patients, including young people.

Among the adverse events linked to the vaccines are thrombosis blood clots and heart inflammation known as myocarditis and pericarditis.

COVID vaccine stocks surge amid fears of new omicron variant

Shares of major COVID vaccine makers surged amid the latest pandemic fears surrounding the new Omicron variant, CNN Business reported.

Moderna climbed more than 20% during Black Friday’s short trading session on Wall Street and increased by an additional 10% on Monday.

Shares of BioNTech, which partners with Pfizer to produce COVID vaccines, soared 14% on Friday and were up 3% Monday, as Pfizer gained 6% Friday.

Investors are hoping the vaccine makers will be able to quickly update their COVID vaccines to offer protection for the Omicron variant.

Moderna said Friday it “will rapidly advance an Omicron-specific booster candidate” while Pfizer said it hoped to have an update of its vaccine ready in 100 days if Omicron shows resistance to its current vaccine.

Moderna CEO predicts a reduction in COVID vaccine effectiveness against Omicron variant

Stéphane Bancel, CEO of Moderna, said in an interview Tuesday current COVID vaccines will likely be much less effective against the new Omicron variant, compared with previous variants, The Washington Post reported.

“I just don’t know how much, because we need to wait for the data,” Bancel said. “But all the scientists I’ve talked to … are, like, ‘This is not going to be good.’”

Bancel said scientists did not expect such a highly mutative variant to emerge for another year or two, noting 32 of the 50 mutations in Omicron involve the spike protein — the area targeted by existing COVID vaccines.

In early March, Dr. Geert Vanden Bossche, a vaccinologist who worked with GSK Biologicals, Novartis Vaccines, Solvay Biologicals, Bill & Melinda Gates Foundation’s Global Health Discovery team in Seattle and Global Alliance for Vaccines and Immunization in Geneva, broke down the dangers of mass vaccination for COVID compared to natural infection and concluded:

“There can be no doubt that continued mass vaccination campaigns will enable new, more infectious viral variants to become increasingly dominant and ultimately result in a dramatic incline in new cases despite enhanced vaccine coverage rates. There can be no doubt either that this situation will soon lead to complete resistance of circulating variants to the current vaccines.”

As The Defender reported on March 26, a combination of lockdowns and extreme selection pressure on the virus-induced by the intense global mass vaccination program might diminish the number of cases, hospitalizations, and deaths in the short term, but will ultimately induce the creation of more mutants of concern.

This is the result of what Vanden Bossche called “immune escape,” which will in turn trigger vaccine companies to further refine vaccines that will add to, not reduce, the selection pressure, producing ever more transmissible and potentially deadly variants.

Vanden Bossche argued the selection pressure would cause greater convergence in SARS-CoV-2 mutations affecting the spike protein of the virus responsible for breaking through the mucosal surfaces of our airways — the route used by the virus to enter the human body — effectively outsmarting the highly specific antigen-based vaccines that are being used and tweaked, dependent on the circulating variants.

Children’s Health Defense asks anyone who has experienced an adverse reaction, to any vaccine, to file a report following these three steps.

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