VAERS data released Friday by the Centers for Disease Control and Prevention included a total of 1,071,856 reports of adverse events from all age groups following COVID vaccines, including 22,607 deaths and 178,994 serious injuries between Dec. 14, 2020, and Jan. 21, 2022.
The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,071,856 reports of adverse events following COVID vaccines were submitted between Dec. 14, 2020, and Jan. 21, 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 22,607 reports of deaths — an increase of 414 over the previous week — and 178,994 reports of serious injuries, including deaths, during the same time period — up 4,130 compared with the previous week.
Excluding “foreign reports” to VAERS, 740,000 adverse events, including 10,316 deaths and 67,496 serious injuries, were reported in the U.S. between Dec. 14, 2020, and Jan. 21, 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 10,316 U.S. deaths reported as of Jan. 21, 19% occurred within 24 hours of vaccination, 24% occurred within 48 hours of vaccination and 61% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated.
In the U.S., 532.4 million COVID vaccine doses had been administered as of Jan. 21, including 312 million doses of Pfizer, 202 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 Jan. 21, 2022, for 5- to 11-year-olds show:
7,052 adverse events, including 152 rated as serious and 3 reported deaths.
The most recent death involves a 7-year-old girl (VAERS I.D. 1975356) from Minnesota who died 11 days after receiving her first dose of Pfizer’s COVID vaccine when she was found unresponsive by her mother. An autopsy is pending.
14 reports of myocarditis and pericarditis (heart inflammation).
24 reports of blood clotting disorders.
U.S. VAERS data from Dec. 14, 2020, to Jan. 21, 2022, for 12- to 17-year-olds show:
27,772 adverse events, including 1,588 rated as serious and 37 reported deaths.
The most recent deaths involve a 13-year-old male (VAERS I.D. 2042005) from an unidentified state who died from a sudden heart attack seven months after receiving his second dose of Moderna, and a 17-year-old female from an unidentified state (VAERS I.D. 2039111) who died after receiving her first dose of Moderna. Medical information was limited and it is unknown if an autopsy was performed in either case.
68 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.
609 reports of myocarditis and pericarditis with 597 cases attributed to Pfizer’s vaccine.
154 reports of blood clotting disorders, with all cases attributed to Pfizer.
U.S. VAERS data from Dec. 14, 2020, to Jan. 21, 2022, for all age groups combined, show:
21% 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 72.7.
As of Jan. 21, 4,925 pregnant women reported adverse events related to COVID vaccines, including 1,575 reports of miscarriage or premature birth.
Of the 3,474 cases of Bell’s Palsy reported, 51% were attributed to Pfizer vaccinations, 41% to Moderna and 8% to J&J.
850 reports of Guillain-Barré syndrome (GBS), with 41% of cases attributed to Pfizer, 30% to Moderna and 28% to J&J.
2,281 reports of anaphylaxis where the reaction was life-threatening, required treatment or resulted in death.
12,704 reports of blood clotting disorders in the U.S. Of those, 5,646 reports were attributed to Pfizer, 4,521 reports to Moderna and 2,490 reports to J&J.
1,542 reports of myocardial infarction.
3,817 cases of myocarditis and pericarditis with 2,348 cases attributed to Pfizer, 1,293 cases to Moderna and 164 cases to J&J’s COVID vaccine.
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