Thursday, November 25, 2021

"'Severe Reactions' to Covid Vaccines are Far More Common Than Official Data Show"

Note:
The original article included many hard to read data tables excluded here. Some data-free paragraphs were also deleted.
Ye Editor

Source:

"The Covid-19 vaccine* debate has been predicated on a number of demonstrable untruths since the very beginning.

No bigger lie has been told to the American public than the vaccines are “safe and effective.”

This ceaseless “safe and effective” mantra has been told to millions of Americans by white labcoat-wearing ‘public health’ officials in countless ad campaigns ...


... Dr. Anthony Fauci hasn’t yet thrown in the towel on proclaiming those people who took the initial round of Covid jabs are no longer “fully vaccinated.”

But his recent pronouncement that “we believe” that boosters “will likely” provide the highest level of protection yet gives otherwise healthy people enough pause to scratch that booster shot appointment off the calendar.

... As Becker News reported in September, well ahead of the Covid curve, there was a developing trend of “more vaccines, more Covid.”

As we have seen in sundry cases around the country since then, high vaccination rates do not translate to lower case rates:

Vermont is the most vaccinated state in the nation at 68% ‘fully vaccinated’ (for now), but nonetheless is seeing a massive spike in coronavirus cases and hospitalizations.

Now, that we’ve established that the vaccines are not as “effective” as was advertised ...

There’s evidence that they are not nearly as “safe,” either.

There have been complaints before that the Vaccine Adverse Event Reporting System (VAERS) is underreporting Covid vaccine reactions,
despite it being a “passive” system.

Nonetheless, there have been over one million adverse events reported after taking the Covid-19 vaccine, according to the VAERS website.
 https://www.medalerts.org/vaersdb/findfield.php?TABLE=ON&GROUP1=CAT&EVENTS=ON&VAX=COVID19

... Richard Baris, also known as the People’s Pundit, is currently one of the best pollsters in the country.

Now, Baris was concerned by the noticeable disparity between the adverse events (AEs) reported in Pfizer’s documents and the VAERS website,

and had taken it upon himself to start polling Americans directly about their vaccine experiences.

He went above and beyond the critical threshold needed for a representative sample of national significance by polling 2,414 registered voters across the country.

... he drilled down enough to check all the boxes on represenative subgroups.

This gives his results a sound 95% confidence interval in terms of their representative value.

... The Baris poll shows that simply the “serious adverse effects” from the Covid vaccines – described as events so serious they “prevent daily activity” – were reported to be 5.2% among all groups.

This spans self-identified Democrat, Republican, and Independent voters. Independent voters had the highest reported serious adverse effect rate at 6.5%.

The extrapolated data would project out at a national scale to around 9.4 million “serious” adverse events, which alone dwarf the VAERS reports by 14 times over.

But if you take all of the events together, a whopping 63% of Americans who take the vaccines have some kind of adverse event.

Since there are 194 million Americans who are reportedly “fully vaccinated,” or nearly 60% of the population, there is no way to square the VAERS reports and the monumental scale of AEs that are communicated by this trustworthy and reliable polling.

It’s not just pollsters who are sounding the alarm on serious Covid vaccine events: Cardiologists are reporting a huge spike in heart inflammation cases to the American Heart Association (AHA).

A cardiac surgeon has circulated a warning to the AHA that heart inflammation markers are drastically increasing in patients in conjunction with increasing mRNA Covid vaccination rates.

The warning to the AHA is clear:
    “Patients had a 1 in 4 risk for severe problems after the vaccines, compared to 1 in 9 before.”

“Recently, with the advent of the mRNA COVID 19 vaccines (vac) by Moderna and Pfizer, dramatic changes in the PULS score became apparent in most patients.

This report summarizes those results,” Dr. Guidy wrote, adding,
    “We conclude that the mRNA [vaccines] dramatically increase inflammation on the endothelium & T cell infiltration of cardiac muscle and may account for the observations of increased thrombosis, cardiomyopathy & other vascular events following vaccination.”

The spike in heart inflammation cases has been particularly prominent among young people. Dr. Jessica Rose, a prominent critic of the universal vaccination agenda, has spoken out forcefully on the issue, only to face censorship in “peer-reviewed journals.”

“Jessica Rose, PhD just had her paper on VAERS analysis of myocarditis rejected after two rounds of review at ‘Reviews in Cardiovascular Medicine,” philanthropist Steve Kirsch, founder of COVID-19 Early Treatment Fund (CETF), noted.

“NO REASON GIVEN.

This is scientific misconduct at its finest by the peer reviewers (not the Journal). Jessica is first-rate.”

“You cannot get any paper published that is anti-vaccine nowadays,” he added.

“Academics will ONLY believe what is peer reviewed.

So the vaccines are safe because there are no papers saying it isn’t, even though the data shows it isn’t.

BUT NOBODY LOOKS AT THE DATA anymore.”

An interview with Aga Wilson of News Voice gave a fuller presentation of Dr. Rose’s views.

“Dr. Jessica Rose, who is normally positive about vaccines, says that VAERS (Vaccine Adverse Event Reporting System), the US database for vaccine injuries, has only managed to collect an estimated 1% of the total number of serious side effects from mRNA injections,’

NewsVoice reported. “VAERS is, unfortunately, a weak system when it comes to how side effect data is handled, says Rose.

She, therefore, divided adverse reactions and side effects into several categories such as neurology, immunology, reproductive organs, and cardiovascular.

In this way, she has created a warning system where it should be easier to see if and in that case how side effects can be linked to the mRNA vaccines.”

“Rose says that the so-called ‘covid vaccines’ are not actual vaccines but rather injections of genetic material,” the report added.

“Several studies have been published, despite attempts to censor these, which show that the spike proteins themselves are very toxic to the body.

These spike proteins are foreign proteins.”

“The fact that millions of people have been injected with these so-called ‘mRNA vaccines’ is to be considered a crime against humanity, Dr. Jessica Rose believes.”

Dr. Rose reports on the adverse events reportage following injection. Of interest, around day 7 there is a significant spike in post-injection adverse events reportage that gets missed because the FDA and CDC refuse to acknowledge that someone is vaccinated until 2 weeks following injection.

This is a “donut hole” in the vaccination side effects reportage. ...

Dr. Rose also provides analysis of the Adverse Events being reported by VAERS in a (slightly dated) September 2021 document.

Dr. Rose notes that the 1108% increase in VAERS reports is not explained by excess vaccine doses.

Here she breaks down the AEs by major categories:
Cardiovascular, neurological, and immunological.
She charts the cumulative changes in the respective metrics below:
In the analysis provided with Steve Kirsch, Dr. Rose attempts to scale out and estimate the “true” Adverse Events cases.
It is important to note that Pfizer’s documents reveal that there should be far more Adverse Events than are being officially reported; however, we cannot say how much more, because Pfizer is redacting its documents that were used for the Emergency Use Authorization by the FDA.

... Food and Drug Administration has provided its first batch of ‘confidential’ documents, in accordance with a FOIA lawsuit by the Public Health and Medical Professionals for Transparency.

The redacted documents were the basis of the FDA’s Emergency Use Authorization of the Pfizer-BioNTech “vaccine*,” and subsequent federal vaccine mandates.

The FDA does not intend to fully release Pfizer’s clinical trials information used to justify its authorization of the ‘vaccine’ for 55 years. 

Two months after the lawsuit was filed, the FDA produced the first 91 pages of the “more than 329,000 pages potentially responsive to Plaintiff’s FOIA request.”

The findings, taken directly from the produced documents ... shows that AEs are much more in line with the critics’ estimation than with the public record.

“It is estimated that approximately [REDACTED] doses of Pfizer BNT162b2 were shipped worldwide from the receipt of the first temporary authorisation for emergency supply on 01 December 2020 through 28 February 2021,” the document states.

“Cumulatively, through 28 February 2021, there was a total of 42,086 case reports (25,379 medically confirmed and 16,707 non-medically confirmed) containing 158,893 events,” the FDA document continues.

“Most cases (34,762) were received from United States (13,739), United Kingdom (13,404) Italy (2,578), Germany (1913), France (1506), Portugal (866).”

... aGeneral Overview of the reported outcomes to the Adverse Events: lists 1223 fatal outcomes in the Relevant Cases.

Interestingly, the age range with the most relevant cases was 31-50 years old, which is not the age group considered to be at high risk from Covid-19.

The figure contains the addendum:

    As shown in Figure 1, the System Organ Classes (SOCs) that contained the greatest number (≥2%) of events in the overall dataset, were
General disorders and administration site conditions (51,335 AEs),
Nervous system disorders (25,957),
Musculoskeletal and connective tissue disorders (17,283),
Gastrointestinal disorders (14,096),
Skin and subcutaneuous tissue disorders (8,476),
Respiratory, thoracic and mediastinal disorders (8,848),
Infections and infestations (4,610),
Injury, poisoning and procedural complications (5,590), and I
nvestigations (3,693).

... One of the documents produced is a Cumulative Analysis of Post-Authorization Adverse Event Reports of [the Vaccine] Received Through 28-Feb-2021, which is a mere 2 ½ months after the vaccine received emergency use authorization (EUA).

This document reflects adverse events following vaccination that have completed Pfizer’s “workflow cycle,” both in and outside the U.S., up to February 28, 2021.

    Pfizer explains, on page 6, that “Due to the large numbers of spontaneous adverse event reports received for the product, [Pfizer] has prioritised the processing of serious cases…”

and that Pfizer “has also taken a [sic] multiple actions to help alleviate the large increase of adverse event reports” including “increasing the number of data entry and case processing colleagues”

and “has onboarded approximately [REDACTED] additional fulltime employees (FTEs).”

Query why it is proprietary to share how many people Pfizer had to hire to track all of the adverse events being reported shortly after launching its product.

... The fact that Pfizer was granted complete immunity from liability with its fraudulent “full authorization” should signal to policy makers and American voters that the entire universal vaccination agenda is fatally flawed.

Since the case is building that vaccines are neither safe, nor effective, and it should be added, do not stop the spread, the vaccine mandates need to stop immediately.

*Since the Pfizer-BioNTech’s product BNT162b2 does not stop the spread of SARS-CoV-2 and marginally lowers transmission, it is more accurately called a prophylactic therapeutic, and not a “vaccine.”