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Health Viewpoints: CDC Data Shows More Than 1.2 Million Covid Vaccine Injuries
By biDaala studio
Health Viewpoints


CDC DATA SHOWS MORE THAN 1.2 MILLION COVID VACCINE INJURIES

BY Megan Redshaw TIMEApril 17, 2022 PRINT
0:0011:57

1



VAERS data released Friday by the Centers for Disease Control and Prevention
included a total of 1,226,314 reports of adverse events from all age groups
following COVID vaccines, including 26,976 deaths and 219,865 serious injuries
between Dec. 14, 2020, and April 8, 2022.

The Centers for Disease Control and Prevention (CDC) today released new data
showing a total of 1,226,314 reports of adverse events following COVID vaccines
were submitted between Dec. 14, 2020, and April 8, 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 26,976 reports of deaths — an increase of 277 over
the previous week — and 219,865 serious injuries, including deaths, during the
same time period — up 2,564 compared with the previous week.

Excluding “foreign reports” to VAERS, 805,921 adverse events, including 12,471
deaths and 79,811 serious injuries, were reported in the U.S. between Dec. 14,
2020, and April 8, 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 12,471 U.S. deaths reported as of April 8, 17% occurred within 24 hours
of vaccination, 21% 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., 564 million COVID vaccine doses had been administered as of April
8, including 334 million doses of Pfizer, 212 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 APRIL 8, 2022, FOR 5- TO 11-YEAR-OLDS
SHOW:

 * 10,216 adverse events, including 242 rated as serious and 5 reported deaths.
 * 18 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.
 * 39 reports of blood clotting disorders.


U.S. VAERS DATA FROM DEC. 14, 2020, TO APRIL 8, 2022, FOR 12- TO 17-YEAR-OLDS
SHOW:

 * 31,048 adverse events, including 1,792 rated as serious and 44 reported
   deaths.
 * 67 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.
 * 651 reports of myocarditis and pericarditis, with 639 cases attributed to
   Pfizer’s vaccine.
 * 166 reports of blood clotting disorders, with all cases attributed to Pfizer.


U.S. VAERS DATA FROM DEC. 14, 2020, TO APRIL 8, 2022, FOR ALL AGE GROUPS
COMBINED, SHOW:

 * 20% 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 73.
 * As of April 8, 5,404 pregnant women reported adverse events related to COVID
   vaccines, including 1,6936 reports of miscarriage or premature birth.
 * Of the 3,647 cases of Bell’s Palsy reported, 51% were attributed
   to Pfizer vaccinations, 40% to Moderna and 8% to J&J.
 * 860 reports of Guillain-Barré syndrome, with 42% of cases attributed to
   Pfizer, 30% to Moderna and 28% to J&J.
 * 2,373 reports of anaphylaxis where the reaction was life-threatening,
   required treatment or resulted in death.
 * 1,671 reports of myocardial infarction.
 * 13,755 reports of blood-clotting disorders in the U.S. Of those, 6,169
   reports were attributed to Pfizer, 4,911 reports to Moderna and 2,654
   reports to J&J.
 * 4,124 cases of myocarditis and pericarditis with 2,531 cases attributed to
   Pfizer, 1,402 cases to Moderna and 181 cases to J&J’s COVID vaccine.


WOMAN DEVELOPS FATAL BRAIN DISEASE AFTER SECOND MODERNA DOSE

Carol Beauchine died from sporadic Creutzfeldt-Jakob Disease (CJD), a rapidly
evolving, fatal degenerative brain disorder she developed after her second dose
of Moderna’s COVID vaccine.

In an exclusive interview with The Defender, Carol’s son, Jeffrey Beauchine,
said it was excruciating to watch his 70-year-old mother — who was healthy until
she got the vaccine — die from a disease he believes the vaccine caused.

Beauchine said Carol received her first dose of Moderna on Feb. 16, 2021, and
didn’t report any complaints. After getting the second dose on March 17, Carol
immediately said she “felt different.” She developed numbness that spread
throughout the entire left side of her body, blindness and hearing loss. She
lost the ability to walk and communicate, and her brain degenerated until she
passed away on Aug. 2, 2021 — just five months after receiving her second dose
of Moderna.



The family submitted a report to VAERS, but the CDC has not followed up on
Carol’s death. The Defender has received numerous reports of people who died
from sporadic CJD after receiving a COVID vaccine — all women who were between
the ages of 60 and 70, including Cheryl Cohen and Jennifer Deason Sprague.


BIDEN ADMINISTRATION EXTENDS COVID PUBLIC HEALTH EMERGENCY NEEDED TO KEEP
VACCINES UNDER EUA

The Biden administration on Wednesday extended the COVID public health
emergency, now two years old, for an additional 90 days — allowing vaccines and
other drugs to remain under Emergency Use Authorization (EUA). Keeping COVID
vaccines and other countermeasures under EUA shields pharmaceutical
companies from liability for the harms caused by their products.

According to Reuters, a public health emergency was initially announced in
January 2020, when the COVID pandemic began. It has been renewed each quarter
since and was due to expire on April 16.

The Department of Health and Human Services (HHS) said in a statement it was
extending the public health emergency and will give states 60 days’ notice prior
to termination or expiration. This may be the last time HHS Secretary Xavier
Becerra extends it, according to policy experts.


PFIZER TO SEEK AUTHORIZATION FROM FDA FOR COVID BOOSTER SHOT FOR KIDS 5 TO 11
YEARS OLD

Pfizer and BioNTech Thursday said they plan to apply for EUA of a COVID booster
dose for healthy 5- to 11-year-olds based on the results of a small study that
has not been published or analyzed by independent experts.

Pfizer said in a press release the third dose of its vaccine produced
significant protection against the Omicron variant in children 5 to 11 in a
small Phase 2/3 clinical trial. The study was based on data from only 140
children 5 through 11 years old who received a booster dose six months after the
second dose of Pfizer-BioNTech’s COVID vaccine as part of the primary series.

Pfizer claimed a closer look at 30 children showed a 36-fold increase in
virus-fighting antibodies — levels high enough to fight the Omicron variant, and
that a third dose was “well tolerated with no new safety signals observed.”

Although Pfizer said more than 10,000 children under the age of 12 have
participated in clinical trials investigating Pfizer’s COVID vaccine, only 140
were selected for the study forming the basis for the company’s EUA request.


CDC LAUNCHES INTERNAL REVIEW OVER FAILED COVID RESPONSE

The CDC announced Monday it was launching a month-long comprehensive agency-wide
review following widespread criticism of the agency’s response to the COVID
pandemic.

The agency plans to evaluate its structure, systems and processes, CDC Director
Dr. Rochelle Walensky told staff in an email obtained by The Washington Post.
Walensky said the goal of the review is to “modernize” the agency and “to
position CDC, and the public health community, for greatest success in the
future.”

The review will be conducted by Jim Mcrae, associate administrator for primary
healthcare at the Health Resources and Services Administration (HRSA). The HRSA
and the CDC are part of the Department of Health and Human Services.

Last month, the CDC’s decision to remove from its data tracker website tens of
thousands of deaths linked to COVID — including nearly a quarter of the deaths
the agency said had occurred among children — eroded public trust in the CDC’s
handling of case counts.

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

Originally published on Children’s Health Defense

© 04/15/22 Children’s Health Defense, Inc. This work is reproduced and
distributed with the permission of Children’s Health Defense, Inc. Want to learn
more from Children’s Health Defense? Sign up for free news and updates from
Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will
help to support us in our efforts.

Views expressed in this article are the opinions of the author and do not
necessarily reflect the views of The Epoch Times.



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Megan Redshaw

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Megan Redshaw is a freelance reporter for The Defender. She has a background in
political science, a law degree and extensive training in natural health.

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