The Weekly US Covid Vaxxes Deaths and Adverse Effects Report By Chris Knight (Florida)

The Centers for Disease Control and Prevention (CDC) Vaccine Adverse Event Reporting System (VAERS), is the principal government-funded system for reporting adverse vaccine reactions in the U.S. New data for this week shows a total of 1,295,329 reports of adverse events following Covid-19 vaccines were submitted between December 14, 2020, and June 3, 2022, an increase of 7,734 adverse events over last week. The data included a total of 28,714 reports of deaths, an increase of 182 over last week, and 236,767 serious injuries, including deaths, during the same time period, an increase of 1,726 compared with last week. Of the 28,714 reported deaths, 18,638 cases were due to Pfizer’s Covid-19 vaccine, 7,524 cases to Moderna and 2,483 cases to Johnson & Johnson (J&J). VAERS has an under-reporting factor estimated to be between 41 and 100.

https://childrenshealthdefense.org/defender/reports-deaths-covid-vaccines-cdc-vaers-data/?utm_source=salsa&eType=EmailBlastContent&eId=8d0570f2-4060-4e47-a4a8-dfc28f5cca11

“The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,295,329 reports of adverse events following COVID-19 vaccines were submitted between Dec. 14, 2020, and June 3, 2022, to the Vaccine Adverse Event Reporting System (VAERS). That’s an increase of 7,734 adverse events over the previous week.

VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.

The data included a total of 28,714 reports of deaths — an increase of 182 over the previous week — and 236,767 serious injuries, including deaths, during the same time period — up 1,726 compared with the previous week.

Of the 28,714 reported deaths, 18,638 cases are attributed to Pfizer’s COVID-19 vaccine, 7,524 cases to Moderna and 2,483 cases to Johnson & Johnson (J&J).

Excluding “foreign reports” to VAERS, 829,329 adverse events, including 13,225 deaths and 83,801 serious injuries, were reported in the U.S. between Dec. 14, 2020, and June 3, 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 13,225 U.S. deaths reported as of June 3, 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., 588 million COVID-19 vaccine doses had been administered as of June 3, including 347 million doses of Pfizer, 222 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 June 3, 2022, for 6-month-olds to 5-year-olds show:

• 1,658 adverse events, including 63 cases rated as seriousand 3 reported deaths.
• 4 reportsof 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.
• 13 reportsof blood clotting disorders.

U.S. VAERS data from Dec. 14, 2020, to June 3, 2022, for 5- to 11-year-olds show:

• 11,133 adverse events, including 292 rated as seriousand 5 reported deaths.
• 22 reportsof myocarditis and pericarditis.
  The Defender has noticed over previous weeks that reports of myocarditis and pericarditis have been removed by the CDC from the VAERS system in this age group. No explanation was provided.
• 43 reportsof blood clotting disorders.

U.S. VAERS data from Dec. 14, 2020, to June 3, 2022, for 12- to 17-year-olds show:

• 32,026adverse events, including 1,834 rated as serious and 44 reported deaths.
• 62 reportsof anaphylaxis among 12- to 17-year-olds where the reaction was life-threatening, required treatment or resulted in death — with 97% of cases attributed to Pfizer’s vaccine.
• 655 reportsof myocarditis and pericarditis with 643 cases attributed to Pfizer’s vaccine.
• 166 reportsof blood clotting disorders with all cases attributed to Pfizer. VAERS reported 167 cases of blood clotting disorders in the 12- to 17-year-old age group last week.

U.S. VAERS data from Dec. 14, 2020, to June 3, 2022, for all age groups combined, show:

• 20% 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 ageof death was 73.
• As of June 3, 5,574 pregnant womenreported adverse events related to COVID-19 vaccines, including 1,743 reports of miscarriage or premature birth.
• Of the 3,615 cases of Bell’s Palsyreported, 51% were attributed to Pfizer vaccinations, 40% to Moderna and 8% to J&J.
• 884 reports of Guillain-Barré syndrome, with 42% of cases attributed to Pfizer, 30% to Modernaand 28% to J&J.
• 2,290 reportsof anaphylaxis where the reaction was life-threatening, required treatment or resulted in death.
• 1,725 reportsof myocardial infarction.
• 14,079 reportsof blood-clotting disorders in the U.S. Of those, 6,291 reports were attributed to Pfizer, 5,048 reports to Moderna and 2,701 reports to J&J.
• 4,223 casesof myocarditis and pericarditis with 2,589 cases attributed to Pfizer, 1,434 cases to Moderna and 186 cases to J&J.
• 10 casesof Creutzfeldt-Jakob disease with 4 cases attributed Pfizer, 5 cases to Moderna and 1 case to J&J.”