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LATEST VAERS DATA SHOW: 5,165 DEATHS REPORTED FOLLOWING COVID VACCINES

by The New Agora | Jun 9, 2021 | Public Notices

LATEST VAERS DATA SHOW: 5,165 DEATHS REPORTED FOLLOWING COVID VACCINES

childrenshealthdefense.org/defender

Originally published on www.childrenshealthdefense.org by Megan Redshaw

06/04/21

VAERS DATA RELEASED TODAY SHOWED 294,801 REPORTS OF ADVERSE EVENTS FOLLOWING
COVID VACCINES, INCLUDING 5,165 DEATHS AND 25,359 SERIOUS INJURIES BETWEEN DEC.
14, 2020 AND MAY 28, 2021

This week’s number of reported deaths among all age groups following
COVIDvaccines passed the 5,000 mark, up 759 from last week, according to data
released today by the Centers for Disease Control and Prevention (CDC). The data
comes directly from reports submitted to the Vaccine Adverse Event Reporting
System (VAERS).

VAERS is the primary government-funded system for reporting adverse
vaccinereactions in the U.S. Reports submitted to VAERS require further
investigation before a causal relationship can be confirmed.

Every Friday, VAERS makes public all vaccine injury reports received as of a
specified date, usually about a week prior to the release date. Today’s data
show that between Dec. 14, 2020 and May 28, a total of 294,801 total adverse
events were reported to VAERS, including 5,165 deaths — an increase of 759 over
the previous week. There were 25,359 serious injuries reported, up 3,822
compared with last week.

Among 12- to 17-year-olds, there were 40 reports of heart inflammation and 16
cases of blood clotting disorders.

In the U.S., 292.1 million COVID vaccine doses had been administered as of May
28. This includes 123 million doses of Moderna’s vaccine, 158 million doses
of Pfizer and 11 million doses of the Johnson & Johnson (J&J) COVID vaccine.

Of the 5,165 deaths reported as of May 28, 24% occurred within 48 hours of
vaccination, 16% occurred within 24 hours and 38% occurred in people who became
ill within 48 hours of being vaccinated.

This week’s data for 12- to 17-year-olds show:

* 4,740 total adverse events, including 117 rated as serious and four reported
deaths among 12 to 17-year-olds. The youngest deaths reported include two
15-year-olds (VAERS I.D. 1187918 and 1242573), a 16-year-old (VAERS
I.D. 1225942) and one 17-year-old (VAERS I.D. 1199455). There were other
reported deaths in children under 17 that could not be confirmed or contained
obvious errors.
* 635 reports of anaphylaxis among 12- to17-year-olds with 97% of cases
attributed to Pfizer’s vaccine, 2% to Moderna and 0.31% (or two cases)
to J&J.
* 40 reports of myocarditis and pericarditis (heart inflammation) all
attributed to Pfizer’s COVID vaccine.
* 16 reports of blood clotting disorders, all attributed to Pfizer.

This week’s total VAERS data, from Dec. 14, 2020, to May 28, 2021, for all age
groups show:

* 17% of deaths were related to cardiac disorders.
* 52% of those who died were male, 45% were female and the remaining death
reports did not include gender of the deceased.
* The average age of death was 74.4.
* As of May 28, 1,831 pregnant women reported adverse events related to COVID
vaccines, including 596 reports of miscarriage or premature birth.
* Of the 2,876 cases of Bell’s Palsy reported, 52% were reported
after Pfizer vaccinations, 41% following vaccination with the Moderna vaccine
and 253 cases, or 9%, of Bell’s Palsy cases were reported in conjunction with
J&J.
* 280 reports of Guillain-Barré Syndrome with 46% of cases attributed to
Pfizer, 40% to Moderna and 20% to J&J.
* 83,684 reports of anaphylaxis with 40% of cases attributed to Pfizer’s
vaccine, 51% to Moderna and 9% to J&J.
* 5,159 reports of blood clotting disorders. Of those, 2,213 reports were
attributed to Pfizer, 1,617 reports to Moderna and 1,289 reports to J&J.

Seven cases of heart inflammation reported in teen boys, new study shows

On June 4, The Defender reported seven boys between the ages of 14 and 19 in the
U.S. reportedly developed chest pain and heart inflammation within four days of
receiving a second dose of the Pfizer vaccine, according to a study published
today in Pediatrics.

Heart imaging tests detected a rare type of heart muscle inflammation called
myocarditis and pericarditis. None of the teens were critically ill but all were
hospitalized.

Only one of the seven boys in the Pediatrics report displayed evidence of a
possible previous COVID infection, and doctors determined none of them had a
rare inflammatory condition linked with COVID or pre-existing conditions. It is
possible myocarditis or pericarditis may be an additional rare adverse event
related to systemic reactogenicity, but currently no causal association has been
established between this vaccine and myopericarditis, the authors concluded.

A search in VAERS revealed 628 cases of myocarditis and pericarditis, among all
age groups reported in the U.S following COVID vaccination between Dec.14, 2020
and May 28. Of the 628 cases reported, 392 cases were attributed to Pfizer, 206
cases to Moderna and 27 cases to J&J’s COVID vaccine.

Of the 628 total cases of heart inflammation, 40 cases occurred in children ages
12 to 17, all attributed to Pfizer’s COVID vaccine.

Israeli health officials find probable link between Pfizer vaccine and heart
inflammation

As The Defender reported June 2, Israeli health officials found a probable link
between Pfizer’s COVID vaccine — which the country has relied on almost
exclusively in its vaccination drive — and dozens of cases of heart inflammation
in young men following the second dose.

A study by Israeli health officials identified 275 cases of myocarditis in
Israel between December 2020 and May 2021, including 148 cases that occurred
within a month after vaccination. Of those 148 cases, 27 occurred after the
first dose and 121 after the second dose. About half of the cases involved
people with previous medical conditions.

Many of the cases were reported among men 16 to 30 years old, and most often in
16- to 19-year-olds. Most of the patients were discharged from the hospital in
less than four days, and 95% of the cases were considered mild.

New research shows COVID vaccine spike protein travels from injection site

On June 3, The Defender reported on research obtained by a group of scientists
showing the COVID vaccine spike protein can travel from the injection site and
accumulate in organs and tissues including the spleen, bone marrow, liver,
adrenal glands and in “quite high concentrations” in the ovaries.

COVID vaccine researchers had previously assumed mRNA COVID vaccines would
behave like traditional vaccines. The vaccine’s spike protein — responsible for
infection and its most severe symptoms — would remain mostly in the injection
site at the shoulder muscle or local lymph nodes.

The new research for the first time provided scientists the opportunity to see
where messenger RNA [mRNA] vaccines go after vaccination.”

Woman who almost died after J&J vaccine stuck with $1 million in medical bills

As The Defender reported June 2, a 38-year-old woman who suffered multiple organ
failure from J&J’s COVID vaccine said victims should be compensated by the
government for taking the risk.

Kendra Lippy was diagnosed with severe blood clots resulting in 33 days of
hospitalization. She suffered organ failure, and was left without most of her
small intestine — and with crippling medical bills.

Lippy’s case was one of the six that led federal agencies to temporarily pause
the J&J shot in mid-April.

Because the government shielded vaccine makers from liability, Lippy can’t sue
J&J. She also doesn’t have a legitimate legal route to sue the government. The
only current option for people who have suffered COVID vaccine injuries is
the Countermeasures Injury Compensation Program (CICP), which turns down most
applicants. Fewer than one in 10 people receive compensation after applying.

According to data from CICP, more than 701 claim filings since 2010 have been
received from individuals requesting compensation for injuries. Of the 701
claims, only 29 claims were compensated totaling $6 million. Another 452 claims
were deemed ineligible. There are 210 cases pending. As of May 26, CICP had
received 152 claims involving COVID vaccines, and 293 involving other
treatments.

Moderna applies for full FDA approval of its COVID vaccine

On June 1, CNBC reported Moderna asked the U.S. Food and Drug Administration
(FDA) for full U.S. approval of its COVID vaccine — the second drugmaker in the
U.S. to seek a biologics license that will allow it to market the shots directly
to consumers. The mRNA vaccine is currently only approved under an Emergency Use
Authorization, which was granted by the FDA in December. The FDA approval
process is likely to take months.

On May 10, the FDA amended the Emergency Use Authorization for Pfizer’s COVID
vaccine to include 12- to 15-year-olds. On May 7, the vaccine maker also applied
for full approval of its vaccine. Currently, only Pfizer’s vaccine is approved
for emergency use in the 12 to 15 age group.

88 days and counting, CDC ignores The Defender’s inquiries

According to the CDC website, “the CDC follows up on any report of death to
request additional information and learn more about what occurred and to
determine whether the death was a result of the vaccine or unrelated.”

On March 8, The Defender contacted the CDC with a written list of
questions about reported deaths and injuries related to COVID vaccines. After
repeated attempts, by phone and email, to obtain a response to our questions, a
health communications specialist from the CDC’s Vaccine Task Force contacted us
on March 29 — three weeks after our initial inquiry.

The individual received our request for information from VAERS, but said she had
never received our list of questions, even though employees we talked to several
times said CDC press officers were working through the questions and confirmed
the representative had received them. We provided the list of questions again
along with a new deadline, but never received a response.

On May 19, a CDC employee said our questions had been reviewed and our inquiry
was pending in their system, but would not provide us with a copy of the
response. We were told we would be contacted by phone or email with the
response.

On June 4, the CDC employee we contacted said our request was pending in the
system, but nobody had responded to our inquiries. We were advised to submit our
questions again, which we have done numerous times.

It has been 88 days since we sent our first email inquiring into VAERS data and
reports.

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

Megan Redshaw

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.

The Children’s Health Defense Team is devoted to the health of people and our
planet. Our mission is to end the childhood health epidemics by working
aggressively to eliminate harmful exposures, hold those responsible accountable,
and establish safeguards so this never happens again. We do what we do for many
reasons, but the one thing we all share is our passionate belief that we have
public health policies and practices that are harming our children. For the
future good health of our children and planet, we call for more research and
transparency. Visit us at www.childrenshealthdefense.org

Disclaimer: This article is not intended to provide medical advice, diagnosis or
treatment. Views expressed here do not necessarily reflect those of GreenMedInfo
or its staff.

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IN TOUCH WITH THE NEWS THAT MATTERS BY SUBSCRIBING TO OUR TOP NEWS OF THE DAY.
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