The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,151,450 reports of adverse events following COVID vaccines were submitted between Dec. 14, 2020, and Feb. 25, 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 24,827 reports of deaths — an increase of 425 over the previous week — and 200,331 reports of serious injuries, including deaths, during the same time period — up 4,128 compared with the previous week.
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.
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Of the 11,312 U.S. deaths reported as of Feb. 25, 18% occurred within 24 hours of vaccination, 22% occurred within 48 hours of vaccination and 60% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated.
In the U.S., 552 million COVID vaccine doses had been administered as of Feb. 25, including 325 million doses of Pfizer, 208 million doses of Moderna and 18 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 Feb. 25, 2022, for 5- to 11-year-olds show:
The most recent death involves an 8-year-old boy (VAERS I.D. 2109625) from Mississippi who died 7 days after his second dose of Pfizer’s COVID vaccine when he was found blue and lifeless at home.
He was taken to the hospital with a full code in process. A pulse was detected several times, but the boy ultimately died in the ICU. It was reported to the doctor who filed the report that the boy died from multisystem inflammatory syndrome. He did not have COVID.
- 17 reports of myocarditis and pericarditis (heart inflammation).
- 32 reports of blood clotting disorders.
U.S. VAERS data from Dec. 14, 2020, to Feb. 25, 2022, for 12- to 17-year-olds show:
The most recent death involves a 13-year-old girl (VAERS I.D. 2115839) from Wisconsin who was severely compromised and received two doses of Pfizer’s COVID vaccine. Although the cause of death wasn’t clear, she appeared to have significant health issues, respiratory distress and heart problems.
- 69 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.
- 648 reports of myocarditis and pericarditis with 631 cases attributed to Pfizer’s vaccine.
- 159 reports of blood clotting disorders, with all cases attributed to Pfizer.
U.S. VAERS data from Dec. 14, 2020, to Feb. 25, 2022, for all age groups combined, show:
- 19% of deaths were related to cardiac disorders.
- 54% of those who died were male, 41% were female and the remaining death reports did not include the gender of the deceased.
- The average age of death was 72.6.
- As of Feb. 25, 5,176 pregnant women reported adverse events related to COVID vaccines, including 1,653 reports of miscarriage or premature birth.
- Of the 3,587 cases of Bell’s Palsy reported, 51% were attributed to Pfizer vaccinations, 40% to Moderna and 8% to J&J.
- 853 reports of Guillain-Barré syndrome, with 41% of cases attributed to Pfizer, 30% to Moderna and 28% to J&J.
- 2,339 reports of anaphylaxis where the reaction was life-threatening, required treatment or resulted in death.
- 1,621 reports of myocardial infarction.
- 13,320 reports of blood clotting disorders in the U.S. Of those, 5,946 reports were attributed to Pfizer, 4,744 reports to Moderna and 2,568 reports to J&J.
- 4,060 cases of myocarditis and pericarditis with 2,505 cases attributed to Pfizer, 1,373 cases to Moderna and 172 cases to J&J’s COVID vaccine.
Pfizer vaccine only 12% effective in kids 5 to 11, study says
A study released Monday showed the effectiveness of Pfizer’s COVID vaccine in 5- to 11-year-olds was only 12% after a seven-week period of observation. Yet, the authors of the study still recommended the vaccine for that age group, stating it was protective against severe disease.
A study released Monday showed the effectiveness of Pfizer’s COVID-19 vaccine in 5- to 11-year-olds was only 12% after a 7-week period of observation. According to New York Times, federal health officials knew about the findings since early February.https://t.co/yW33Z7JePh
— Robert F. Kennedy Jr (@RobertKennedyJr) March 2, 2022
They also proposed the recommended dose for 5- to 11-year-olds was too small, suggesting a higher dose might solve the problem.
Some scientists at the CDC and FDA pushed for the data to be made public before an FDA meeting, scheduled for Feb. 15, to review Pfizer’s application for Emergency Use Authorization of a three-dose regimen of its vaccine for infants and children 6 months to 5 years old — but the study’s findings were only made public this week.
The FDA on Feb. 11 abruptly postponed the meeting to review Pfizer’s application for infants and children under 5, stating Pfizer didn’t have enough data on the efficiency of a third dose for that age group.
In an article published March 1, Dr. Madhava Setty, senior science editor at The Defender, examined the data in the study and outlined two flaws in the authors’ conclusions: 1) that the vaccines prevent severe disease in this age group, and 2) that increasing the dose might be appropriate.
Judge clears way for Pfizer whistleblower lawsuit
A whistleblower lawsuit alleging fraud during Pfizer’s COVID vaccine trials is moving forward, after a district court judge unsealed the complaint, including 400 pages of exhibits.https://t.co/qgNImhN5Ov
— Robert F. Kennedy Jr (@RobertKennedyJr) March 2, 2022
Jackson worked for Ventavia for a brief period in 2020, before being fired after she filed a complaint with the FDA over alleged indiscretions she observed during the vaccine trials.
She also gave The BMJ a cache of internal company documents, photos and recordings highlighting alleged wrongdoing by Ventavia.
Jackson filed the complaint in the U.S. District Court, Eastern District of Texas, Beaumont Division, under the False Claims Act.
The lawsuit includes several charges of fraud and retaliation on the part of both Ventavia and Pfizer. The complaint remained under seal until Feb. 10, when U.S. District Court Judge Michael Truncale ordered it unsealed.
Husband of woman who died from J&J shot speaks out
The husband of an Oregon woman who died last year from a blood-clotting disorder — two weeks after receiving J&J’s COVID vaccine — spoke out publicly this week about his wife’s death.
U.S. health officials continue to say blood-clotting disorders like one that killed 52-year-old Monica Melkonianare two weeks after the J&J vaccine are rare — despite thousands of vaccine-induced blood-clotting events reported to CDC.https://t.co/QqgqgJY6tE
— Robert F. Kennedy Jr (@RobertKennedyJr) March 2, 2022
Stan Thomas told NBC News he’s fighting to ensure his wife’s sacrifice is not forgotten.
Monica Melkonian, 52, received her J&J shot at a vaccination clinic on April 7, 2021 — the same day the CDC and FDA temporarily paused the vaccine to investigate reports of a rare blood-clotting disorder called vaccine-induced thrombotic thrombocytopenia.
Melkonian’s most notable symptoms included a persistent headache and pain behind her left eye before she experienced a seizure, stroke and ultimately died from the condition.
Booster shots causing more injuries than expected in Israel
More Israelis are experiencing injuries and reactions following COVID booster shots than the country’s passive reporting system shows, according to a survey conducted by the Israeli Ministry of Health (MOH).
The MOH conducted an active survey of booster shot recipients to collect data on adverse events associated with booster doses, then compared the survey data to the data available from the country’s passive reporting system.
Out of 4,000 people who participated in the survey, results showed six of 2,049 respondents were admitted to the hospital following the booster shot, and a significant number of people reported worsening of their underlying health conditions.
Extrapolated to the millions of booster doses that have been administered, that’s 270,000 hospitalizations per 92 million booster doses administered in the U.S. and 13,000 hospitalizations per 4.5 million booster shots administered in Israel.
The MOH survey also found reports of allergic reactions, menstrual irregularities, neurological injuries, injection-site reactions and general adverse events.
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Will America-First News Outlets Make it to 2023?
Things are looking grim for conservative and populist news sites.
There’s something happening behind the scenes at several popular conservative news outlets. 2021 was bad, but 2022 is proving to be disastrous for news sites that aren’t “playing ball” with the corporate media narrative. It’s being said that advertisers are cracking down, forcing some of the biggest ad networks like Google and Yahoo to pull their inventory from conservative outlets. This has had two major effects. First, it has cooled most conservative outlets from discussing “taboo” topics like Pandemic Panic Theater, voter fraud, or The Great Reset. Second, it has isolated those ad networks that aren’t playing ball.
Certain topics are anathema for most ad networks. Speaking out against vaccines or vaccine mandates is a certain path to being demonetized. Highlighting voter fraud in the 2020 and future elections is another instant advertising death penalty. Throw in truthful stories about climate change hysteria, Critical Race Theory, and the border crisis and it’s easy to understand how difficult it is for America-First news outlets to spread the facts, share conservative opinions, and still pay the bills.
Without naming names, I have been told of several news outlets who have been forced to either consolidate with larger organizations or who have backed down on covering certain topics out of fear of being “canceled” by the ad networks. I get it. This is a business for many of us and it’s not very profitable. Those of us who do this for a living are often barely squeaking by, so loss of additional revenue can often mean being forced to make cuts. That means not being able to cover the topics properly. Its a Catch-22: Tell the truth and lose the money necessary to keep telling the truth, or avoid the truth and make enough money to survive. Those who have chosen survival simply aren’t able to spread the truth properly.
We will never avoid the truth. The Lord will provide if it is His will. Our job is simply to share the facts, spread the Gospel, and educate as many Americans as possible while exposing the forces of evil.
To those who have the means, we ask that you please donate. We have options available now, but there is no telling when those options will cancel us. We have our GivingFuel page. There have been many who have been canceled by PayPal, but for now it’s still an option. Your generosity is what keeps these sites running and allows us to get the truth to the masses. We’ve had great success in growing but we know we can do more with your assistance.
Thank you, and God Bless!
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