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FDA ignored evidence of Autoimmune Disease & Vaccine-Associated Enhanced Disease in the Confidential Pfizer Documents

(by The Exposé) – The confidential Pfizer documents, that the U.S. Food and Drug Administration (FDA) has been forced to publish by court order, reveal that Pfizer presented evidence of Covid-19 vaccine recipients suffering auto-immune disease and Vaccine-Associated Enhanced Disease as adverse events, but the FDA chose to ignore it.

The Pfizer Covid-19 injection uses a technology that prior to the end of December 2020, had never before been authorised for use in Humans. It is known as mRNA.

And there’s a pretty good reason as to why it had never been authorised for use in Humans. During animal trials for SARS and MERS, it had the opposite of its intended effect and actually worsened disease by inducing antibody-dependent enhancement.Eighteen months after the administration of the injections in the trials, all the animals had died.

Yet, despite this, the Pfizer jab was granted emergency-use authorisation all around the world and administered to millions.

Why?

Well apparently, it was to protect people against a disease that statistically kills less than 0.2% of those it infects, the vast majority being elderly, vulnerable and having existing underlying conditions.

But even there it has failed.

Take Australia for example. As of June 2022, nearly 90% of Australia is considered fully vaccinated, yet the country is currently riding the largest wave of Covid-19 deaths since March 2022. And according to data from March 2022, at least 4 in every 5 of those deaths are among the fully vaccinated.

This data not only suggests that the Covid-19 injections don’t work, it actually suggests the Covid-19 injections make recipients worse, just like the same technology did during animal trials for a vaccine against SARS and MERS.But data forcibly published by the U.S. Food and Drug Administration (FDA) reveals all of this could have been avoided if only they’d actually bothered to read the documents submitted by Pfizer.

The 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 June 1st 2022.

One of the documents contained in the data dump is ‘reissue_5.3.6 postmarketing experience.pdf’. Page 11 of the confidential document contains data on important potential risks, with one of these being Vaccine-Associated Enhanced Disease (V-AED).

What is V-AED?

Vaccine-associated enhanced disease (V-AED) occurs when an individual who has received a vaccine, develops a more severe presentation of that disease when subsequently exposed to that virus, compared with when infection occurs without prior vaccination.

Disease enhancement has previously been associated with dengue virus infection and was previously observed in humans with inactivated whole-virus vaccines against respiratory syncytial virus (RSV) and measles virus in the 1960s.

Previous animal trials of experimental vaccines against SARS-CoV-1 and MERS-CoV have also been shown to induce a more serious disease when subsequently exposed to the virus.

Pfizer Fraud

It can be difficult to distinguish between vaccine failure (also known as breakthrough disease) and V-AED. Identification of a case of VAED requires the recognition that a clinical presentation is different, atypical, modified or more severe in comparison to the natural disease presentation. Read Full Article >

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