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COVID-19

Even as Adoption of Jabs Fades, More Than 8,000 NEW Covid “Vaccine” Injuries Reported to VAERS

The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,255,355 reports of adverse events following COVID-19 vaccines were submitted between Dec. 14, 2020, and April 29, 2022, 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 27,758 reports of deaths — an increase of 226 over the previous week — and 226,703 serious injuries, including deaths, during the same time period — up 1,937 compared with the previous week. There were 8,224 additional total adverse events reported to VAERS over the previous week.

Excluding “foreign reports” to VAERS, 813,021 adverse events, including 12,779 deaths and 81,271 serious injuries, were reported in the U.S. between Dec. 14, 2020, and April 29, 2022.

Foreign reports are reports foreign subsidiaries send to U.S. vaccine manufacturers. Under U.S. Food and Drug Administration (FDA) 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 12,779 U.S. deaths reported as of April 29, 16% occurred within 24 hours of vaccination, 20% occurred within 48 hours of vaccination and 59% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated.

In the U.S., 575 million COVID-19 vaccine doses had been administered as of April 29, including 339 million doses of Pfizer, 217 million doses of Moderna and 19 million doses of Johnson & Johnson (J&J).

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 April 29, 2022, for 5- to 11-year-olds show:

U.S. VAERS data from Dec. 14, 2020, to April 29, 2022, for 12- to 17-year-olds show:

  • 31,504 adverse events, including 1,808 rated as serious and 44 reported deaths.
    The most recent reported death involves a 14-year-old girl from Tennessee (VAERS I.D. 2238618) who died after receiving her second dose of Pfizer’s COVID-19 vaccine. According to the VAERS report, the girl had a previous history of cancer but was hospitalized 29 days after receiving her second dose of Pfizer with severe COVID-19 and COVID pneumonia. She became “critically ill,” developed respiratory failure and bradycardia and later died.
  • 65 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.
  • 650 reports of myocarditis and pericarditis — two fewer than last week — with 638 cases attributed to Pfizer’s vaccine.
  • 166 reports of blood clotting disorders — 1 fewer than last week — with all cases attributed to Pfizer.

U.S. VAERS data from Dec. 14, 2020, to April 29, 2022, for all age groups combined, show:

However, Brian Hooker, Ph.D., P.E., Children’s Health Defense chief scientific officer and professor of biology at Simpson University, had a different take on the news.

“It seems like the FDA pays lip service to the fact that the spike protein can cause clotting, and to the widespread reports of clotting, by punishing Janssen, who has become the ‘whipping boy’ of the COVID-19 vaccine manufacturers through the pandemic,” Hooker said.

The decision comes about five months after the CDC recommended mRNA vaccines Moderna and Pfizer over J&J for booster doses.

In April 2021, federal health agencies paused distribution of J&J’s vaccine to investigate reported cases of blood clotting disorders occurring in those who received the shot. But regulators lifted the pause 10 days later and added a warning to instructions for its use.

Evidence suggests that even after a vaccinated person has a breakthrough infection, that individual still does not acquire the same level of protection against subsequent exposures that an unvaccinated person acquires.

The announcement followed an April 25 ruling by Judge Mitchell L. Beckloff overruling the district’s motion to dismiss a lawsuit brought in by CHD-CA and PERK against LAUSD alleging the district lacked the legal authority to impose a COVID-19 vaccine requirement on its students aged 12 years and older.

Judge Beckloff also overruled the district’s motion to dismiss other claims, recognizing that CHD-CA and PERK had presented legitimate claims that could proceed in court.

On Jan. 14, LAUSD voted to delay implementation of the mandate and removal of students until the fall of 2022. CHD-CA will hold a rally on May 10, when the LAUSD board votes to delay implementation of the mandate until July 2023.

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

© 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.



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