by Megan Redshaw, Childrens Health Defense:
VAERS data released Friday by the Centers for Disease Control and Prevention show 1,418,220 reports of adverse events from all age groups following COVID-19 vaccines, including 31,074 deaths and 258,480 serious injuries between Dec. 14, 2020, and Sept. 16, 2022.
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VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.
The data included a total of 31,074 reports of deaths — an increase of 139 over the previous week — and 258,480 serious injuries, including deaths, during the same time period — up 1,253 compared with the previous week.
There were a total of 563 reports of adverse events following the new bivalent booster COVID-19 vaccine as of Sept. 16, 2022. The data included a total of 5 deaths and 31 serious injuries.
Of the 31,074 reported deaths, 19,934 cases are attributed to Pfizer’s COVID-19 vaccine, 8,385 cases to Moderna, 2,704 cases to Johnson & Johnson (J&J) and no cases yet reported for Novavax.
Excluding “foreign reports” to VAERS, 868,175 adverse events, including 14,531 deaths and 90,422 serious injuries, were reported in the U.S. between Dec. 14, 2020, and Sept. 16, 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 14,531 deaths reported as of Sept. 16, 7% occurred within 24 hours of vaccination and 15% occurred within 48 hours of vaccination.
In the U.S., 600 million COVID-19 vaccine doses had been administered as of Sept. 14, including 363 million doses of Pfizer, 231 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.
VAERS data from Dec. 14, 2020, to Sept. 16, 2022, for 6-month-olds to 5-year-olds show:
- 3,843 adverse events, including 169 cases rated as serious and 6 reported deaths.
- 5 reports of myocarditis and pericarditis (heart inflammation).
- The CDC uses a narrowed case definition of “myocarditis,” which excludes cases of cardiac arrest, ischemic strokes and deaths due to heart problems that occur before one has the chance to go to the emergency department.
- 26 reports of blood clotting disorders.
- 43 reports of seizures.
VAERS data from Dec. 14, 2020, to Sept. 16, 2022, for 5- to 11-year-olds show:
- 14,115 adverse events, including 665 rated as serious and 28 reported deaths.
- 45 reports of myocarditis and pericarditis.
- 67 reports of blood clotting disorders.
- 180 reports of seizures.
VAERS data from Dec. 14, 2020, to Sept. 16, 2022, for 12- to 17-year-olds show:
- 39,472 adverse events, including 4,277 rated as serious and 120 reported deaths.
- According to the CDC, “VAERS data available to the public include only the initial report data to VAERS. Updated data which contains data from medical records and corrections reported during follow up are used by the government for analysis. However, for numerous reasons including data consistency, these amended data are not available to the public.”
- 269 reports of anaphylaxis among 12- to 17-year-olds where the reaction was life-threatening, required treatment or resulted in death.
- 1,310 reports of myocarditis and pericarditis with 1,158 cases attributed to Pfizer’s vaccine.
- 300 reports of blood clotting disorders with 277 cases attributed to Pfizer.
- 26 cases of postural orthostatic tachycardia syndrome (POTS) with all cases attributed to Pfizer’s vaccine.
VAERS data from Dec. 14, 2020, to Sept. 16, 2022, for all age groups combined, show:
- 16% of deaths were related to cardiac disorders.
- 53% of those who died were male, 42% were female and the remaining death reports did not include the gender of the deceased.
- The average age of death was 72.
- As of Sept. 16, 8,471 pregnant women reported adverse events related to COVID-19 vaccines, including 4,898 reports of miscarriage or premature birth.
- Of the 16,353 cases of Bell’s Palsy reported, 73% were attributed to Pfizer vaccinations, 22% to Moderna and 5% to J&J.
- 2,968 reports of Guillain-Barré syndrome, with 64% of cases attributed to Pfizer, 19% to Moderna and 17% to J&J.
- 10,015 reports of anaphylaxis where the reaction was life-threatening, required treatment or resulted in death.
- 4,756 reports of myocardial infarction.
- 43,030 reports of blood-clotting disorders. Of those, 29,522 reports were attributed to Pfizer, 9,659 reports to Moderna and 3,789 reports to J&J.
- 23,926 cases of myocarditis and pericarditis with 18,186 cases attributed to Pfizer, 5,304 cases to Moderna and 410 cases to J&J.
- 67 cases of Creutzfeldt-Jakob disease with 54 cases attributed to Pfizer, 12 cases to Moderna and 1 case to J&J.
- 534 cases of POTS with 395 cases attributed to Pfizer, 119 cases to Moderna and 21 cases to J&J.
Children’s Health Defense (CHD) asks anyone who has experienced an adverse reaction, to any vaccine, to file a report following these three steps.
Canadian woman dies 7 minutes after booster shot, coroner rules ‘natural causes’
A Canadian woman on Sept. 14 died suddenly in a drug store within minutes of receiving the new bivalent COVID-19 booster shot, according to her daughter.
Carol Pearce texted her daughter, Stephanie Foster, at 12:31 p.m. to say she received her booster shot and was waiting the recommended 15 minutes at the drug store. At 12:38 p.m., Pearce was unconscious.
An eyewitness told SASKTODAY.ca she was in the store when she heard screaming and crying. “They were saying in the store that it was about seven minutes,” after Pearce got the booster shot that she collapsed on the floor, the witness said.
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