CDC Admits It Never Monitored VAERS for COVID Vaccine Safety Signals

In a stunning development, the Centers for Disease Control and Prevention (CDC) last week admitted — despite assurances to the contrary — the agency never analyzed the Vaccine Adverse Event Reporting System (VAERS) for safety signals for COVID-19 vaccines.

The admission was revealed in response to a Freedom of Information Act (FOIA) request submitted by Children’s Health Defense (CHD).

In September 2021, I published an article in The Defender in which I used the CDC’s published methodology to analyze VAERS for safety signals from COVID-19 vaccines.

The signals were loud and clear, leading me to wonder “why is nobody listening?”

Instead, I should have asked, “Is anybody even looking for them?”

After that article was published, I urged CHD’s legal team to submit a FOIA request to the CDC about its VAERS monitoring activities.

Since CDC officials stated publicly that “COVID-19 vaccine safety monitoring is the most robust in U.S. history,” I had assumed that at the very least, CDC officials were monitoring VAERS using the methods they described in a briefing document posted on the CDC website in January 2021 (and updated in February 2022, with minor changes).

I was wrong.

The lynchpin of their safety monitoring was to mine VAERS data for safety signals by calculating what are known as proportional reporting ratios (PRR’s).

This is a method of comparing the proportion of different types of adverse events reported for a new vaccine to the proportion of those events reported for an older, established vaccine.

If the new vaccine shows a significantly higher reporting rate of a particular adverse event relative to the old one, it counts as a safety signal that should then trigger a more thorough investigation.

The briefing document states, “CDC will perform PRR data mining on a weekly basis or as needed.”

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The Latest Tragedy: Sudden Adult Death Syndrome

According to the British Heart Association, there are about 500 cases of SADS in the UK each year.5 The British Office for National Statistics, on the other hand, show far fewer cases.6 The ONS lists a total of 128 cases of SADS (all age groups, whether listed as cardiac-related or unknown) in 2016, 77 cases in 2017, 70 in 2018, 107 in 2019 and 139 cases in 2020.

While data on SADS incidence for 2021 and 2022 are hard to come by, incidence has apparently risen sufficiently enough to cause concern in some countries. Before the pandemic, SADS was the acronym for sudden arrhythmia death syndrome, which was rare and with scant research on it except to mention that it accounted for about 30 percent of unexpected cardiac deaths among young people.7

But today, it’s no longer rare and SADS is virtually on steroids as the numbers of sudden deaths in young adults pile up around the world. The numbers are so concerning that in Australia, for example, the Melbourne Baker Heart and Diabetes Institute is setting up a new SADS registry “to gain more information” about the phenomenon.8,9

According to a spokesperson, there are approximately 750 SADS cases per year in Australia. In the U.S., the average annual death toll from SADS is said to be around 4,000.10

Since the rollout of the COVID jabs, the news has been chockful of reports of young, healthy and often athletic people dying “for no reason” and doctors claim to be “baffled” by it. Doctors and scientists in Australia are even urging everyone under the age of 40 to get their hearts checked, even if they’re healthy and fit.11

Any thinking person, on the other hand, can clearly see the correlation between the shots, which are now well-known for their ability to cause heart inflammation, and the rise in sudden death among young and healthy people.

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White House Health Official Makes False Claim About COVID-19 Vaccines

White House official on June 20 made a false claim about COVID-19 vaccines while encouraging parents to get their young children vaccinated.

Dr. Ashish Jha, the White House’s COVID-19 coordinator, said that “there have not been any serious side effects of these vaccines,” which is not true.

Severe allergic reactions, blood clotting, heart inflammation, and paralysis are among the serious side effects linked to the three COVID-19 vaccines available in the United States.

“There is a well-documented risk of myocarditis from the COVID vaccine, especially in young men and adolescent boys, and an elevated risk of clotting in young women with the Moderna vaccine,” Dr. Jay Bhattacharya, a professor of medicine at Stanford University, told The Epoch Times in an email.

“It’s not right for government scientific advisors to downplay documented risks of the vaccine because it ultimately undermines confidence in public health,” Bhattacharya added.

The White House did not return a request for comment.

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Pfizer Documents reveal at least 800 people never finished the COVID Vaccine Trial due to Death, Injury or Withdrawn Consent

The US Food and Drug Administration (FDA) attempted to delay the release of Pfizer’s COVID-19 vaccine safety data for 75 years despite approving the injection after only 108 days of safety review on December 11th, 2020.

But in early January 2022, Federal Judge Mark Pittman ordered them to release 55,000 pages per month. They released 12,000 pages by the end of January.

Since then, PHMPT has posted all of the documents on its website. The latest drop happened on 1st June 2022.

One of the documents contained in the latest data dump is ‘125742_S1_M5_5351_c4591001 fa interim discontinued patients.pdf’.

The document provides a 112-page list of subjects who withdrew from the phase 1 clinical trial of the Pfizer Covid-19 injection, and provides a vague description as to why.

The first 14 pages list 102 subjects who withdrew from the study. This equates to an average of 7.2 subjects per page. So based on a further 93 pages detailing withdrawn subjects this equates to approximately 780 people who withdrew from the first phase of the clinical trial alone. The actual number could be slightly more or slightly less.

Many of the subjects mysteriously revoked consent to continue in the trial due to reasons such as re-reading the consent form and deciding it is not what they had originally agreed to.

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COVID vaccines appear to cause abnormally long blood clots, says pathologist

Unusually long blood clots are being found in people who received COVID-19 vaccines, according to Dr. Ryan Cole of Cole Diagnostics in Boise, Idaho.

Cole’s laboratory receives tissue samples from morticians across the country. He reports that they are finding long blood clots — including several that are inches-long and even a couple that are a foot long — in corpses that contained the COVID vaccine.

Liberty Counsel, a religious freedom legal advocacy nonprofit currently representing military members seeking vaccine mandate exemptions, recently interviewed Cole. His lab “is able to determine the difference between a spike protein caused by the virus and a spike protein caused by the COVID shots, which are demonstrably different and much more pronounced and serious,” according to the organization.

Cole told Greg Hunter on USAWatchdog earlier this month that a Stanford University study found that, unlike a COVID infection, which leaves the body in a week or two, the vaccine causes the spike protein to remain in the body longer.

“[T]hose who had a natural infection cleared the virus within that first week or two — their body had the ability to clear it,” Cole said.

“But when you put the synthetic sequence in, the body is not clearing it,” he explained. “It’s persistently making spike protein. And that sequence is persisting, and then it’s damaging the organs chronically over time, it’s damaging the immune cells chronically over time, it’s causing clots … chronically over time.”

With mRNA vaccines, the spike protein can stay “up to 8 weeks postvaccination in some cases,” according to the study.

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1,287,595 Injuries Reported After COVID Shots, Vaccine Injury Compensation Programs ‘Overwhelmed’

The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,287,595 reports of adverse events following COVID-19 vaccines were submitted between Dec. 14, 2020, and May 27, 2022, to the Vaccine Adverse Event Reporting System (VAERS). That’s an increase of 9,615 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 28,532 reports of deaths — an increase of 220 over the previous week — and 235,041 serious injuries, including deaths, during the same time period — up 2,347compared with the previous week.

Excluding “foreign reports” to VAERS, 825,454 adverse events, including 13,150 deaths and 83,454 serious injuries, were reported in the U.S. between Dec. 14, 2020, and May 27, 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 13,150 U.S. deaths reported as of May 27, 16% occurred within 24 hours of vaccination, 20% 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., 586 million COVID-19 vaccine doses had been administered as of May 27, including 346 million doses of Pfizer, 221 million doses of Moderna and 19 million doses of Johnson & Johnson (J&J).

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Studies Link Incurable Prion Disease With COVID-19 Vaccine

Studies on COVID-19 vaccines have suggested links between Creutzfeldt-Jakob disease (CJD)—an incurable and fatal prion disease—and getting the COVID-19 vaccine.

A recent French pre-print on CJD and COVID-19 vaccination has suggested that the COVID-19 vaccine may have contributed to the emergence of a new type of sporadic CJD disease that is a lot more aggressive and rapid in disease progression as compared to the traditional CJD.

CJD is a rare disease caused by an abnormal protein in the brain called a prion.

Prions naturally occur in the brain and are usually harmless, but when they become diseased or misfolded, they will affect nearby prions to also become misshapen, leading to deterioration of brain tissue and death.

The disease is incurable as once one prion becomes infected, it will continue to propagate to other prions with no treatment capable of stopping its progress.

The majority of people with CJD have sporadic CJD; they become infected for no apparent reason. However, small subsets of people are diagnosed due to inheritance.

Sporadic CJD, though occurring at random, has been linked to consumption of meat that has been infected with diseased prions, such as affecting individuals that ingest beef from a cow that has been infected.

Though the Omicron variant of COVID-19 does not carry a prion region in its spike protein, the first Wuhan COVID-19 variant has a prion region on its spike protein. A U.S. study indicates that the prion area is able to interact with human cells.

Therefore, when the Wuhan variant’s spike protein gene information was made into a vaccine as part of the mRNA and adenovirus vaccines, the prion region was also incorporated.

As part of the natural cellular process, once the mRNA is incorporated into the cells, the cell will turn the mRNA instructions into a COVID-19 spike protein, tricking the cells into believing that it has been infected so that they create an immunological memory against a component of the virus.

However, the biological process of translating mRNA information into proteins is not perfect and immune to mistakes.

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FDA Flags Heart Inflammation Risk Over Novavax COVID-19 Vaccine

Staff with the U.S. Food and Drug Administration (FDA) on Friday flagged the risk of heart inflammation following the administration of the Novavax COVID-19 vaccine, although they concluded the shot reduces the risk of mild-to-severe COVID-19.

In the company’s nearly 30,000 patient trial, conducted between December 2020 and September 2021, there were four cases of myocarditis, a type of heart inflammation also associated with mRNA vaccines, detected within 20 days post-vaccination. One patient in the trial reported myocarditis after receiving a placebo.

“These events raise the concern for a causal association with this vaccine, similar to the association documented with mRNA COVID19 vaccines,” FDA staff wrote in briefing documents that were released on Friday.

They continued: “Data from passive surveillance during post-authorization use in other countries also indicate a higher than expected rate of myocarditis and pericarditis (mainly pericarditis) associated with the vaccine. However, interpretation of these passive surveillance data is not straightforward, and further evaluation is needed to inform the risk of myocarditis and pericarditis associated with this vaccine, and their outcomes, as additional data emerge over time.”

The agency said it has asked Novavax to flag the risk of myocarditis and pericarditis, another type of inflammation of the heart, as an identified risk in its documentation. Data from Novavax’s trial was acquired before the Omicron and Delta variants spread across the world.

“Based on the efficacy estimate in the clinical trial of this vaccine,” the FDA staff wrote, “it is more likely than not that the vaccine will provide some meaningful level of protection against COVID-19 due to Omicron, in particular against more severe disease.”

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Pfizer and Medicine Regulators hid dangers of Covid-19 Vaccination during Pregnancy due to Study finding increased risk of Birth Defects & Infertility

A ‘Freedom of Information’ request alongside an in-depth dive into the only pregnancy/fertility study performed on the Pfizer Covid-19 injection has revealed that Medicine Regulators and Pfizer chose to publicly cover-up alarming abnormalities of the developing foetus and falsely downgraded the actual risk of Covid-19 vaccination during pregnancy by suppressing documented findings of the clinical data.

These decisions led to medical professionals, who are far too trusting of Medicine Regulators, to wrongly inform pregnant women that the Covid-19 injections are perfectly safe during pregnancy, leading to many pregnant women feeling pressured to get vaccinated.

This fraud and deception has caused at least 4,113 foetal deaths due to Covid-19 vaccination in the USA alone, and a further study shows Covid-19 vaccination actually increases the risk of suffering a miscarriage by at least 1,517%.

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