‘Falsified Data’: Pfizer Vaccine Trial Had Major Flaws, Whistleblower Tells BMJ

A whistleblower involved in Pfizer’s pivotal phase III Covid-19 vaccine trial has leaked evidence to a notable peer-reviewed medical publication that poor practices at the contract research company she worked for raise questions about data integrity and regulatory oversight.

 

Brook Jackson, a now-fired regional director at Ventavia Research Group, revealed to The BMJ that vaccine trials at several sites in Texas last year had major problems – including falsified data, broke fundamental rules, and were ‘slow’ to report adverse reactions.

When she notified superiors of the issues she found, they fired her.

A regional director who was employed at the research organisation Ventavia Research Group has told The BMJ that the company falsified data, unblinded patients, employed inadequately trained vaccinators, and was slow to follow up on adverse events reported in Pfizer’s pivotal phase III trial. Staff who conducted quality control checks were overwhelmed by the volume of problems they were finding. After repeatedly notifying Ventavia of these problems, the regional director, Brook Jackson, emailed a complaint to the US Food and Drug Administration (FDA). Ventavia fired her later the same day. Jackson has provided The BMJ with dozens of internal company documents, photos, audio recordings, and emails. -The BMJ …

https://www.zerohedge.com/covid-19/falsified-data-pfizer-vaccine-trial-had-major-flaws-whistleblower-tells-peer-reviewed

“A Rogue FDA With Blood On Its Hands”

You know I don’t use the !IMPORTANT! tag lightly, so please read this whole post.

There are an awfully lot of people who have lost loved ones and others have been badly damaged by the CV fiasco. They are going to be furious when they find out about this. They’re gonna want to meet up with the Faustian Mr.Fauci and Luciferian other secret society lackeys who contributed to so much loss and so many tragedies.

Excerpt from a new book by Peter Navarro:

Now, you might think that the top doctors and scientists at the US FDA might be smart enough to distinguish between early and late-treatment use of hydroxychloroquine and shape their policies accordingly. Yet you would be wrong.

Indeed, the FDA committed one of the worst blunders of the entire pandemic by taking what amounted to a rogue and foolish action in defiance of both President Trump and the secretary of the Department of Health and Human Services, Alex Azar. Here’s the story behind this important part of the story.

On March 23, four days after President Trump had promised that the FDA would expedite the use of hydroxychloroquine, Azar and his deputy at HHS, Bob Kadlec, gave several FDA bureaucrats very clear and explicit instructions to make hydroxychloroquine widely available to the American public as an early CCP Virus treatment on an outpatient basis. (As shown by the use of hydroxychloroquine in other countries, early-use outpatient treatment would be an important key to interrupting the exponential spread of the virus and minimizing deaths in the United States.)*

Nonetheless, five days later, those very same FDA bureaucrats—including FDA commissioner Stephen Hahn and his eventual replacement, Janet Woodcock—completely countermanded the POTUS-Azar-Kadlec order. Instead, on March 28, the FDA issued a rogue directive restricting the use of hydroxychloroquine to the late treatment of hospitalized patients. 

With its rogue directive, the FDA effectively ensured that hydroxychloroquine would be diverted from its best possible use as an early treatment for outpatients to its worst possible use as a late-treatment medicine for hospitalized patients. At least in the court of public opinion, that single decision was tantamount if not to murder, then certainly to negligent homicide.

Now I would like to tell you that I uncovered a very good reason in my subsequent investigation as to why Hahn and Woodcock, with the apparent help of Dr. Rick Bright, would make such an egregious decision. Yet in the absence of a smoking gun, all I can do is surmise that the decision was either gross incompetence or an intentional attempt by the Deep Administrative State to sabotage President Trump’s hydroxychloroquine policy. Both are nearly unimaginable.

Either way, there is considerable blood on the hands of the FDA for that decision alone. Yet there would be even more blood on Anthony Fauci’s hands…

More at https://www.thegatewaypundit.com/2021/11/exclusive-excerpt-navarro-book/ and much more, of course, in the new Peter Navarro book In Trump Time; A Journal of America’s Plague Year

The Inquisition: “I’m not an anti-vaxxer but ….”

Seriously?   Her life is wrecked and she feels the need to say she’s not an anti-vaxxer?   Is this a religion or what?

https://www.bitchute.com/video/y5yv9p0jN04g/

Australian Independent Press Network
One on one interview with Talija Raffone (known as Nat) about her severe adverse reactions.
Doctors cannot give exemption to second dose and now she must take it up with the medical board.
Here is her TikTok account so you can see her before and afters. https://vm.tiktok.com/ZSejaHBP5/
If you would like to support Nat in anyway please contact her or please help her finance her recovery here https://www.paypal.com/paypalme/natalieraffone