Global Research / Megan Redshaw
The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,418,220 reports of adverse events following COVID-19 vaccines were submitted between Dec. 14, 2020, and Sept. 16, 2022, to the Vaccine Adverse Event Reporting System (VAERS). That’s an increase of 10,811 adverse events over the previous week.
VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.
The data included a total of 31,074 reports of deaths — an increase of 139 over the previous week — and 258,480 serious injuries, including deaths, during the same time period — up 1,253 compared with the previous week.
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 14,531 deaths reported as of Sept. 16, 7% occurred within 24 hours of vaccination and 15% occurred within 48 hours of vaccination.
In the U.S., 600 million COVID-19 vaccine doses had been administered as of Sept. 14, including 363 million doses of Pfizer, 231 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.
VAERS data from Dec. 14, 2020, to Sept. 16, 2022, for 6-month-olds to 5-year-olds show:
- 3,843 adverse events, including 169 cases rated as serious and 6 reported deaths.
- 5 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.
- 26 reports of blood clotting disorders.
- 43 reports of seizures.
VAERS data from Dec. 14, 2020, to Sept. 16, 2022, for 5- to 11-year-olds show:
- 14,115 adverse events, including 665 rated as serious and 28 reported deaths.
- 45 reports of myocarditis and pericarditis.
- 67 reports of blood clotting disorders.
- 180 reports of seizures.
VAERS data from Dec. 14, 2020, to Sept. 16, 2022, for 12- to 17-year-olds show:
- 39,472 adverse events, including 4,277 rated as serious and 120 reported deaths.
- According to the CDC, “VAERS data available to the public include only the initial report data to VAERS. Updated data which contains data from medical records and corrections reported during follow up are used by the government for analysis. However, for numerous reasons including data consistency, these amended data are not available to the public.”
- 269 reports of anaphylaxis among 12- to 17-year-olds where the reaction was life-threatening, required treatment or resulted in death.
- 1,310 reports of myocarditis and pericarditis with 1,158 cases attributed to Pfizer’s vaccine.
- 300 reports of blood clotting disorders with 277 cases attributed to Pfizer.
- 26 cases of postural orthostatic tachycardia syndrome (POTS) with all cases attributed to Pfizer’s vaccine.
VAERS data from Dec. 14, 2020, to Sept. 16, 2022, for all age groups combined, show:
- 16% of deaths were related to cardiac disorders.
- 53% of those who died were male, 42% were female and the remaining death reports did not include the gender of the deceased.
- The average age of death was 72.
- As of Sept. 16, 8,471 pregnant women reported adverse events related to COVID-19 vaccines, including 4,898 reports of miscarriage or premature birth.
- Of the 16,353 cases of Bell’s Palsy reported, 73% were attributed to Pfizer vaccinations, 22% to Moderna and 5% to J&J.
- 2,968 reports of Guillain-Barré syndrome, with 64% of cases attributed to Pfizer, 19% to Moderna and 17% to J&J.
- 10,015 reports of anaphylaxis where the reaction was life-threatening, required treatment or resulted in death.
- 4,756 reports of myocardial infarction.
- 43,030 reports of blood-clotting disorders. Of those, 29,522 reports were attributed to Pfizer, 9,659 reports to Moderna and 3,789 reports to J&J.
- 23,926 cases of myocarditis and pericarditis with 18,186 cases attributed to Pfizer, 5,304 casesto Moderna and 410 cases to J&J.
- 67 cases of Creutzfeldt-Jakob disease with 54 cases attributed to Pfizer, 12 cases to Moderna and 1 case to J&J.
- 534 cases of POTS with 395 cases attributed to Pfizer, 119 cases to Moderna and 21 cases to J&J.
Canadian woman dies 7 minutes after booster shot, coroner rules ‘natural causes’
Carol Pearce texted her daughter, Stephanie Foster, at 12:31 p.m. to say she received her booster shot and was waiting the recommended 15 minutes at the drug store. At 12:38 p.m., Pearce was unconscious.
An eyewitness told SASKTODAY.ca she was in the store when she heard screaming and crying. “They were saying in the store that it was about seven minutes,” after Pearce got the booster shot that she collapsed on the floor, the witness said.
A spokesperson from Saskatchewan Health told SASKTODAY.ca on Thursday Pearce died from natural causes.
“The Saskatchewan coroner’s service has investigated this instance and determined that the person died from natural causes,” Dale Hunter, a communications consultant from the Saskatchewan Ministry of Health said in an email.
“I do not believe this was caused from natural causes,” Foster said. “My Mom had no health conditions. I believe had she not gotten that Covid shot then she would be here with us today!”
The family said when Pearce left for her appointment, she was happy and healthy.
Reportedly 15 minutes after getting a shot in Saskatoon @ Shoppers Drug Mart, Stephanie Foster's mother dies. https://t.co/iZoBTeikcl pic.twitter.com/ZwIwnVvjge
— wlctv.ca (@wlctv_ca) September 17, 2022
CDC predicts COVID boosters for kids by mid-October
The agency said in a document released Tuesday it will issue a recommendation in early- to mid-October if the FDA authorizes the modified booster for this age group.
The CDC said it expects Pfizer-BioNTech’s bivalent booster to be available for children ages 5 to 11 and Moderna’s bivalent booster to be available for children ages 6 to 17, pending authorization by the FDA.
The bivalent booster targets both the original Wuhan strain no longer in circulation and the Omicron BA.4/BA.5 subvariants. The CDC expects pre-orders of the Pfizer booster to begin next week even though the FDA has not yet signed off on the vaccine for this age group.
Moderna’s booster is the same formula used for children and adults and will not require a separate pre-order period, the agency said.
Woman’s brain inflammation caused by Moderna COVID vaccine, case study confirms
The authors of the report said the vaccine caused the woman’s condition.
According to the case report, when the woman arrived at the hospital she had a fever, followed by generalized tonic-clonic seizures that lasted for approximately five minutes and a postictal (post-seizure) phase of confusion that lasted approximately 30 minutes.
While in the ER, she had two more generalized seizures and was stable. Upon admission to the hospital, a lumbar puncture was performed revealing significant lymphocytosis.
She then developed anisocoria, a condition in which the pupil of one eye differs in size from the pupil of the other eye. An urgent CT scan of the head showed possible temporal lobe hypodensities (darker areas on the CT scan). A head MRI showed features suggestive of limbic encephalitis. A subsequent electroencephalogram showed severe post-seizure encephalitic changes.
While hospitalized, the patient developed abnormal behavior associated with limbic encephalitis and was diagnosed with autoimmune limbic encephalitis.
Researchers concluded the patient’s limbic encephalitis — which occurred quickly after COVID-19 vaccination — is an uncommon side effect of the vaccine based on the timing of symptoms and absence of other identifiable causes.
U.S. Supreme Court to consider case against COVID vaccine mandate for New York City employees
The U.S. Supreme Court on Oct. 7 will consider a New York Police Department detective’s challenge to the city’s COVID-19 vaccine mandate for municipal employees.
Supreme Court Justice Clarence Thomas granted the request by the detective, Anthony Marciano, after Justice Sonia Sotomayor initially rejected it. Marciano’s challenge seeks to strike down the mandate for all city workers — including firefighters, police and teachers.
According to data from the mayor’s office, as of Aug. 30, 1,761 city workers have been fired for not getting the vaccine. That number is likely higher after the New York City Department of Education this month fired another 850 teachers and other staff, bringing the total to nearly 2,000 school employees fired for failure to comply with the mandate, according to the New York Post.
The Supreme Court’s decision to consider Marciano’s request came one day after New York Mayor Eric Adams rescinded the city’s COVID-19 vaccine mandate for private employers and student athletes — but not municipal employees.
Woman develops blood clots, hallucinations, mini-strokes after Pfizer shots
In April 2021, Cathy Nagy’s 84-year-old mother-in-law received her first dose of the Pfizer vaccine.
According to Nagy, “about a week-and-a-half later, Marilyn experienced an episode of hallucinations, seeing people outside who were not there.”
Nagy told The Defender:
“Marilyn’s family attributed [the episode] to her dementia, even though she had not had any prior episodes … [They] did not make a connection to the vaccination.”
But the family’s opinion changed a few weeks later, after Marilyn got her second Pfizer shot and “had a more dramatic reaction,” experiencing “another episode of hallucinations that same day, extreme weakness and pain in her leg,” Nagy said.
Marilyn seemed to recover, but over the coming weeks, she continued to experience occasional hallucinations, and an increased decline in her cognition, Nagy said, prompting a visit to a neurologist.
An MRI “revealed she was experiencing blood clots, bleeding and mini-strokes in her brain, and she was sent directly to the ER for observation and treatment,” Nagy said.
At the hospital, Marilyn was administered blood-thinning medications and appointments were scheduled “with several specialists.”
About a month later, she developed deep vein thrombosis in her left leg, which according to Nagy, was “the same leg that had been experiencing pain since her second vaccine.”
“Her right leg also became painfully swollen, although no blood clot was found,” Nagy said.
Biden says ‘pandemic is over’ but mandates, federal health emergency remain in effect
President Joe Biden’s Sept. 18 statement that the COVID-19 pandemic is “over” prompted questions about why his administration hasn’t ended the federal public health emergency and how the government or employers can continue to mandate Emergency Use Authorized vaccines.
In an interview aired Sunday on “60 Minutes,” President Joe Biden declared the COVID-19 “pandemic is over,” in the first such statement by a prominent political figure in the U.S. Biden made the comment from the North American International Auto Show in Detroit, which was held for the first time since 2019.
In his remarks, Biden, using the auto show as a point of reference, stated:
“We still have a problem with COVID. We’re still doing a lotta work on it … but the pandemic is over.
“If you notice, no one’s wearing masks. Everybody seems to be in pretty good shape. And so I think it’s changing. And I think this is a perfect example of it.”
Sarah Lovenheim, a spokesperson for the U.S. Department of Health and Human Services (HHS), said the federal public health emergency “remains in effect” and that a 60-day notice would be provided by the agency before it is rescinded.
The earliest possible date when the emergency declaration would be lifted is in late November — well past the current Oct. 15 expiration date.
HHS first declared the public health emergency on Jan. 31, 2020, and renewed it 10 times since, most recently on July 15. In order for COVID-19 vaccines to be authorized for emergency use, a “public health emergency” must remain in effect.
Woman with heart condition injured by Pfizer shot after being forced to choose between job and vaccine
When her employer in 2021 mandated all employees get the COVID-19 vaccine, Heather Elkins, who had a pre-existing heart condition, requested a medical exemption.
But the Oregon Department of Human Services turned down her application — even though Elkins had transitioned, in 2020, to a permanent work-from-home employee.
Elkins, 45, told The Defender she was reluctant to get the vaccine in part because of the lack of long-term safety data but also because she saw reports of people developing heart issues.
The reactions she experienced after the first shot didn’t qualify her for a medical exemption from the second shot, she said.
So despite continued efforts to secure a medical exemption, Elkins received her second Pfizer shot on Oct. 3, 2021, and experienced “the same severe reaction as with the first dose.”
A year later, Elkins continues to experience symptoms that affect her ability to work.
Elkins told The Defender:
“To date, I’m experiencing all the same issues in addition to other symptoms like brain fog, horrible joint pain, pins and needles sensations, painful nerve zaps, shakiness and tremors in my hands and feet, and vision issues.
“I’ve now been mostly confined to my bed for the last 11 months, unable to do minimal activities because of my debilitating symptoms.”