BOMBSHELL evidence: FDA and Pfizer conspired to hide thousands of adverse events and deaths caused by the COVID jab

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bombshell-evidence(NaturalHealth365)  While most doctors and scientists have gone along with the jab-pushing agenda, more and more physicians and medical experts are stepping forward to warn about the potential harm mRNA COVID injections inflict on the human body.  Despite their tireless efforts to alert the population, millions have decided to roll up their sleeve and take the shot in the arm without raising a single question about the safety profile of the experimental drugs.

Stakeholders of the COVID pandemic have routinely downplayed countless reports of adverse effects and jab-related deaths.  Voices of the thousands injured or killed by the shot have been silenced, their pain and suffering swept under the rug.  Beyond doubt, mainstream media, social media companies, Big Pharma, and government authorities have done a tremendous job at convincing unsuspecting citizens to become part of this global jab experiment by hiding the potential risks and exaggerating the purported benefits of these injections.

At some point, everyone must wonder and ask the question: what are they covering up?

Thanks to a nonprofit made up of public health and medical professionals, scientists, and journalists, we now have smoking-gun evidence that Pfizer and the U.S. Food and Drug Administration (FDA) knew in early 2021 that the jabs were killing thousands – all the while coercing and bribing people into taking the deadly shot.

SHOCKING Pfizer report: Document submitted to the FDA reveals over 42,000 case reports including 1,223 deaths following Pfizer’s mRNA jab in only 90 days post-EUA

The document obtained by the nonprofit Public Health and Medical Professionals for Transparency (PHMPT) shows without a doubt that Pfizer knew early on about the thousands of adverse events and deaths people reported after taking the experimental shot.

(In case you wonder why the FDA would release such incriminating information, know that the agency fought tooth and nail to prevent it from coming to light.)

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The report titled Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162B2) Received Through 28-Feb-2021 was obtained by PHMPT through a Freedom of Information Act (FOIA) request submitted on August 27th, 2021 – four days after Pfizer received FDA approval for ages 16 and over for its product marketed under the name of Comirnaty.

The FOIS request included “all data and information for the Pfizer Vaccine enumerated in 21 CFR § 601.51(e) with the exception of publicly available reports on the Vaccine Adverse Events Reporting System.”  Let’s take a look at the report’s content, shall we?

Report reveals: Three times as many women harmed by the Pfizer jab than men

The 38-page document contains confidential data Pfizer submitted to the FDA as part of its post-authorization safety report.  Here are some of the horrifying findings:

  • Through February 28th, 2021, there were 42,086 case reports containing 158,893 adverse events
  • Most cases were received from the US, UK, Italy, Germany, France, Portugal, and Spain
  • 29,914 cases involved women; 9,182 men, which means three times as many women were harmed by the jab than men. Although the number of women and men who took the injection is unknown, seeing three times as many women harmed than men could indicate a gender-specific jab risk
  • 1,223 cases had a fatal outcome
  • The age group most significantly affected by the adverse effects was 31 to 50, with 13,886 cases

What type of adverse events were people experiencing?

Besides “general disorders,” the most frequent mRNA jab adverse reactions were nervous system disorders, with 25,957 reports, followed by adverse events affecting the musculoskeletal, gastrointestinal, and respiratory systems.  Take a look at the chart below to get a more accurate idea of the diverse adverse effects reported.

Pfizer informed the FDA, its mRNA jab could cause “enhanced disease”

It is important to point out that under section 3.1.2. Summary of Safety Concerns in the US Pharmacovigilance Plan Pfizer cites Vaccine-Associated Enhanced Disease (VAED), including Vaccine-associated Enhanced Respiratory Disease (VAERD), as “important potential risks” of the injection.  What that means is that the FDA knew the jab could not only sicken but even kill vaxxed individuals contracting COVID later on.

FDA knew the mRNA jab could kill unborn babies

If the above has not been sickening enough, here is another ‘difficult to face reality.’  In the Use in Pregnancy and Lactation section, it becomes disturbingly obvious that the jab killed many unborn babies through spontaneous abortions, premature birth with neonatal death, spontaneous abortion with intrauterine death, and more.

In light of the released report, it is not only undeniable that Pfizer’s jab harmed thousands, but also that the FDA ignored the deaths and destruction and labeled the product “safe and effective.”

How can the American people trust the FDA to protect public health?  Shouldn’t top officials be held accountable?  And, if so, when?!

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