JUST IN: Over 42,000 Adverse Reaction Reports Revealed In First Batch Of Pfizer Vax Docs

(TeaParty.org Exclusive) – According to a brand new report from Infowars, the FDA’s painfully slow release of information related to Pfizer’s coronavirus vaccine has finally started to bear some fruit and it’s not good news for the company, despite the trickle of just 500 pages of documentation per month out of a total of 329,000 pages, which is probably going to take all the way until 2076 to complete.

That’s an obscenely long time, right? Makes you wonder why on earth the company is trying so hard to ensure that this information isn’t released all at once. It’s almost like, — gasp — they have something to hide!

A report from ZeroHedge revealed that the FDA actually asked a federal judge to make the public release of all of the information and data it has relied upon in order to approve the coronavirus vaccine developed by Pfizer until the year 2076. Yes, that’s correct. They actually want the general public to wait 55 years for this information to be released.

“As explained in a prior article, the FDA repeatedly promised “full transparency” with regard to Covid-19 vaccines, including reaffirming “the FDA’s commitment to transparency” when licensing Pfizer’s COVID-19 vaccine,” the report said.

“With that promise in mind, in August and immediately following approval of the vaccine, more than 30 academics, professors, and scientists from this country’s most prestigious universities requested the data and information submitted to the FDA by Pfizer to license its COVID-19 vaccine,” ZeroHedge continued.

So how did the FDA respond? They didn’t produce anything. Then, in September a firm filed a lawsuit against the FDA on behalf of this group in order to get access to the information requested.

“Instead, two days ago, the FDA asked a federal judge to give it until 2076 to fully produce this information. The FDA asked the judge to let it produce the 329,000+ pages of documents Pfizer provided to the FDA to license its vaccine at the rate of 500 pages per month, which means its production would not be completed earlier than 2076. The FDA’s promise of transparency is, to put it mildly, a pile of illusions [ZH, we note that the FDA justifies this by claiming that the rate of 500 pages per month “is consistent with processing schedules entered by courts across the country in FOIA cases,” and blames the plaintiffs for “its own broad FOIA request”],” the report continued.

“It took the FDA precisely 108 days from when Pfizer started producing the records for licensure (on May 7, 2021) to when the FDA licensed the Pfizer vaccine (on August 23, 2021). Taking the FDA at its word, it conducted an intense, robust, thorough, and complete review and analysis of those documents in order to assure that the Pfizer vaccine was safe and effective for licensure. While it can conduct that intense review of Pfizer’s documents in 108 days, it now asks for over 20,000 days to make these documents available to the public,” the report stated.

Yeah, nothing weird about that at all, right? These people are wacked in the head if they think people don’t notice this garbage.

Kyle Becker first reported there was a total of 42,086 cases where adverse effects from the vaccine were reported, with 25,379 of these medically confirmed, 16,707 non-medically confirmed, that spans 158,893 total events.

More than 25,000 of these events have been classified as “Nervous system disorders,” which is a stunningly large number. At that time, not a single page had been released (screen shot here).

“Since the vaccine has been publicly administered, there have been over 913,000 reports of adverse events in the OpenVAERS global database,” Infowars reported (screen shot here).

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