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   Extremely American
   
 * 
 * * Jul 17
   * 
   * 8 min read




FDA ADDS NEW WARNING TO J&J VACCINE: VAERS REPORTS 11,000 DEATHS RELATED TO
COVID VACCINES










11,000 Deaths after Covid Vaccines reported to CDC, as FDA adds new warning to
J&J Vaccine






Source: The Defender – Megan Redshaw; July 16, 2021






VAERS data released today by the CDC showed a total of 463,457 reports of
adverse events from all age groups following COVID vaccines, including 10,991
deaths and 48,385 serious injuries between Dec. 14, 2020 and July 9, 2021.






Data released by the CDC included 463,457 reports of injuries and deaths, across
all age groups, following COVID vaccines.

















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Data released today by the Centers for Disease Control and Prevention (CDC)
included 463,457 reports of injuries and deaths, across all age groups,
following COVID vaccines — an increase of more than 25,000 compared with the
previous week.






The data comes directly from reports submitted to the Vaccine Adverse Event
Reporting System (VAERS), the primary government-funded system for reporting
adverse vaccine reactions in the U.S.






Every Friday, VAERS makes public all vaccine injury reports received as of a
specified date, usually about a week prior to the release date. Reports
submitted to VAERS require further investigation before a causal relationship
can be confirmed.






Data released today show that between Dec. 14, 2020 and July 9, 2021, a total of
463,457 total adverse events were reported to VAERS, including 10,991 deaths —
an increase of 1,943 over the previous week. There were 48,385 serious injuries
reported during the same time period — up 7,370 compared with the previous week.






In the U.S., 333 million COVID vaccine doses had been administered as of July 9.
This includes: 135 million doses of Moderna’s vaccine, 184 million doses of
Pfizer and 13 million doses of the Johnson & Johnson (J&J) COVID vaccine.






Of the 10,991 deaths reported as of July 9, 22% occurred within 48 hours of
vaccination, 15% occurred within 24 hours and 37% occurred in people who became
ill within 48 hours of being vaccinated.






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






- 14,003 total adverse events, including 866 rated as serious and 14 reported
deaths. Two of the nine deaths were suicides.



- The most recent reported death includes a 13-year-old boy (VAERS I.D. 1431289)
with a previous history of COVID who suffered cardiac arrest and died 17 days
after vaccination with Pfizer.






Other reports include two 13-year-old boys (VAERS I.D. 1406840 and 1429457) who
died two days after receiving a Pfizer vaccine, three 15-year-olds (VAERS I.D.
1187918, 1382906 and 1242573), three 16-year-olds (VAERS I.D. 1420630, 1225942
and 1386841) and three 17-year-olds (VAERS I.D. 1199455, 1388042 and 1420762).






- 2,040 reports of anaphylaxis among 12- to 17-year-olds with 99% of cases
attributed to Pfizer’s vaccine, 1.1% to Moderna and 0.2% (or four cases) to J&J.



- 377 reports of myocarditis and pericarditis (heart inflammation) with 373
attributed to Pfizer’s vaccine.



- 65 reports of blood clotting disorders, with 64 attributed to Pfizer and 1
attributed to Moderna.






This week’s total VAERS data, from Dec. 14, 2020 to July 9, 2021, for all age
groups combined show:






- 23% of deaths were related to cardiac disorders.



- 50% 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 75.



- As of July 9, 2,857 pregnant women reported adverse events related to COVID
vaccines, including 1072 reports of miscarriage or premature birth.



- Of the 5,049 cases of Bell’s Palsy reported, 63% were attributed to Pfizer
vaccinations, 35% to Moderna vaccine and 5% to J&J.



- 445 reports of Guillain-Barré Syndrome, with 51% of cases attributed to
Pfizer, 37% to Moderna and 17% to J&J.



- 127,421 reports of anaphylaxis with 48% of cases attributed to Pfizer’s
vaccine, 45% to Moderna and 7% to J&J.



- 9,471 reports of blood clotting disorders. Of those, 4,998 reports were
attributed to Pfizer, 2,845 reports to Moderna and 1,582 reports to J&J.



- 1,991 cases of myocarditis and pericarditis with 1,336 cases attributed to
Pfizer, 599 cases to Moderna and 52 cases to J&J’s COVID vaccine.






Experts warn of ‘huge risk’ as Moderna launches COVID vaccine trials for
pregnant women






Moderna will study its COVID vaccine in pregnant women, according to a posting
on ClinicalTrials.gov. The observational study, expected to begin July 22, will
enroll about 1,000 females over age 18 who will be studied over a 21-month
period.






Women who received a Moderna vaccine during the 28 days prior to their last
menstrual period, or at any time during pregnancy, are eligible.






The brief summary of the trial states the main goal is “to evaluate the outcomes
of pregnancy in females exposed to the Moderna COVID-19 vaccine (mRNA-1273)
during pregnancy.”






Currently, the CDC says pregnant women can get a COVID vaccine. But the agency
also acknowledges there is limited data available about the safety of COVID
vaccines for people who are pregnant.



Tell Schools/Universities No Vaccine Mandates for Children/Young Adults!






“Pregnant women are taking what may be a huge risk with the COVID vaccine,” said
Jennifer Margulis, Ph.D., author of “Your Baby, Your Way.” Margulis said in an
email to The Defender, there is no evidence COVID vaccines are safe, but ample
evidence suggesting it is dangerous to expose pregnant women and unborn babies
to drugs and interventions that can disrupt immunity.






Lyn Redwood, RN, MSN and president emerita of Children’s Health Defense, said
it’s “bass-ackwards to release the vaccine to pregnant women before doing a
clinical trial or proper animal studies.”






FDA added warning to J&J vaccine of ‘serious but rare’ autoimmune disorder






On July 13, the FDA added a new warning on J&J’s (Janssen) COVID vaccine to
include information pertaining to an observed increased risk of Guillain-Barré
Syndrome (GBS) following vaccination.






According to an FDA news release, GBS is a neurological disorder in which the
body’s immune system damages nerve cells, causing muscle weakness or, in the
most severe cases, paralysis.






Based on an analysis of VAERS data, there have been 100 preliminary reports of
GBS following vaccination with J&J’s vaccine. Of these reports, 95 were serious
and required hospitalization. There was one reported death.






While the cause of GBS is not fully known, it often follows infection with a
virus and has been linked to other vaccines. The FDA concluded the benefits of
the vaccine outweigh any danger, but included the proviso in fact sheets about
the drug for providers and patients.






The CDC’s Advisory Committee on Immunization Practices (ACIP) is expected to
discuss the GBS cases during an upcoming meeting, the CDC said.






Coroner says vaccine not to blame for man’s death after Pfizer— wife not
convinced






A healthcare worker who died four days after his second dose of Pfizer’s COVID
vaccine was killed by heart disease, according to the Orange County, California
coroner.






As The Defender reported this week, Tim Zook, an x-ray technologist at South
Coast Global Medical Center in Santa Ana, was hospitalized Jan. 5 — just hours
after being vaccinated. Zook’s wife, Rochelle, told the Orange County Register
her husband’s health rapidly deteriorated after receiving his second dose of
Pfizer’s vaccine. He died Jan. 9.






An autopsy report released Wednesday found Zook’s heart was severely enlarged,
thicker than normal and dilated. “There is a focus of severe coronary artery
disease,” according to the report, which also said Zook’s heart valves showed
mild-to-moderate calcium deposits.






The autopsy report concluded the official cause of death was “hypertensive and
atherosclerotic heart disease with severe cardiomegaly [enlarged heart] and
heart failure.”






Rochelle Zook said she is not convinced her husband’s death is unrelated to the
vaccine. He was “quite healthy,” she said shortly after her husband’s death.
Rochelle Zook preserved samples of her husband’s tissue for future testing,
hoping to learn more as data about vaccines emerge in years to come.






Woman’s sudden paralysis linked to J&J vaccine






A Houston woman spent 22 days in the hospital after getting a COVID vaccine and
then developing GBS, ABC 13 reported July 14. After Jamie Walton got the J&J
vaccine, she started feeling numbness and tingling in her feet and hands.






“I know my body and I knew something wasn’t right, so I kept trying to go to
different doctors and I kept being told, ‘You’re dehydrated. You’re fine,'”
Walton said. “One doctor told me I had anxiety.”






The otherwise healthy woman ended up paralyzed from the waist down and lost her
ability to walk. Walton went to the emergency room twice and met with several
doctors before her diagnosis was confirmed. She was hospitalized for 22 days,
had to learn how to walk again and do other basic movements. Her case was
reported to VAERS.






Pfizer fails to convince FDA on immediate need for boosters






Pfizer executives met privately this week with U.S. senior scientists and
regulators to press their case for quick authorization of COVID booster vaccines
amid pushback from federal health agencies who last week said the extra doses
are not needed.






Officials said after the meeting that more data — and possibly several more
months — would be needed before regulators could determine whether booster shots
were necessary, The Defender reported.






The meeting was largely seen as a courtesy after Pfizer’s announcement last week
that it would seek Emergency Use Authorization for its booster shot led to
unusual pushback from the U.S. Food and Drug Administration (FDA) and CDC.






Woman with ‘life-altering’ injuries after COVID vaccine teams up with U.S.
senators to demand answers






A Utah woman and two U.S. senators are teaming up to get answers from federal
health agencies about life-altering injuries people have experienced after
receiving a COVID vaccine, The Defender reported July 7.






Brianne Dressen, preschool teacher from Utah, was injured after participating in
AstraZeneca’s COVID vaccine clinical trial in November 2020. She accumulated
more than $250,000 in medical bills as a result of injuries she believes were
caused by the vaccine.






After experiencing severe symptoms and neurological decline, Dressen spent
months teaching herself how to walk, eat and form sentences again — all while
she traveled in search of answers.






Dressen, along with other people who said they were injured by vaccines but
“repeatedly ignored” by the medical community, participated last month in a news
conference held by Sen. Ron Johnson (R-Wis).






Following the news conference, Johnson and Utah Sen. Mike Lee wrote a letter to
the CDC and FDA after the agencies ignored requests for assistance and answers
from families injured by COVID vaccines.






Lee and Johnson said widespread lack of acknowledgement of adverse events
following receipt of a COVID vaccine has made it nearly impossible for some
individuals to obtain the medical treatment they need, and that risks must be
disclosed to the medical community and general public.






In the letter, Lee and Johnson asked the FDA and CDC about the adverse events
suffered during clinical trials, disclosed in the FDA’s Emergency Use
Authorization Memorandum for the Pfizer, Moderna and Johnson & Johnson vaccines,
as well as reported injuries from the U.S. AstraZeneca trial.






They also asked the CDC whether it is working with physicians and researchers at
the FDA, National Institutes of Health or other medical research bodies to
provide the various individuals who experienced adverse effects vaccine
treatment and care.






130 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. We have made
repeated attempts, by phone and email, to obtain a response to our questions.






Despite multiple phone and email communications with several people at the CDC,
and despite being told that our request was in the system and that someone would
respond, we have not yet received answers to any of the questions we submitted.
It has been 130 days since we sent our first email to the CDC requesting
information.






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






1. For U.S. residents, first file your report with the Vaccine Adverse Event
Reporting System (VAERS), the official site of the U.S. Department of Health and
Human Services (HHS).



2. Go to VaxTracker to file a report. This is an outside source vs. government.



3. Using this page on the CHD website, share the information you reported to
VaxxTracker and VAERS, including the reaction you suffered and the vaccine you
received. Also see our Covid-19 Vaccine Reactions page which lists all the
reactions that have been submitted.






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