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DailyClout Opinion Pfizer Documents Analysis
Opinion

International Experts Testify Again, This Time in Brazil (Porto Alegre Seminar)

August 14, 2023 • by Chris Flowers, MD, MBBS, FRCR, FSBI

The brave representative Fernanda Barth led the hearing in the Municipality of Porto Alegro along with John Kage. Many of the names you have come to love and respect were there, and I was asked by Dr Naomi Wolf to represent the 3,500 volunteers of the WarRoom/DailyClout Pfizer Document Investigations.

August 15, 2023, update: The video of this hearing is now available in the video below. It is in Portuguese. To turn on subtitles in your language of choice, click the cog-like Settings button at the bottom right of the video window. Then, click the arrow to the right of Subtitles, click Auto-Translate, and select the language you desire for the subtitles.


 

The presentation by Dr James Thorp was a great introduction to the findings of the WarRoom posse, as I then followed with our presentation – The Pfizer Documents ‘in their own words’ (They knew and did not tell us!).

After giving my credentials, I summarized why my breast cancer screening and treatment experience was relevant.

Do you ever remember ANY discussion about the risks vs. benefits of the vaccine? The narrative was certainly that it was SAFE and EFFECTIVE against this killer virus, so anything was justified in their minds.

Even a response from Chat-GPT is reasonable and should have been part of a dialogue before the mass inoculation with this dangerous platform. I asked it to write a paragraph on the risks vs. the benefits, and I have done a separate post about its response. See my previous substack posting on the experiment.

Introducing the work of the WarRoom/DailyClout volunteers –

What did the FDA try to hide from the public?

The mRNA-Lipid Nanoparticle platform was new in humans (even though known to be dangerous after being experimented with since the 1980s).

The devastating finding that the LNPs accumulate over time in reproductive organs (ovaries and testes).

See Report 42: Pfizer’s EUA Granted Based on Fewer Than 0.4% of Clinical Trial Participants. FDA Ignored Disqualifying Protocol Deviations to Grant EUA.

The CONTROL GROUP (those who received placebos) were given experimental therapy at the end of the trial, so there are no normal people to compare with anymore.

The Brazilian doctors were most interested in the EUAs for children, as they are being mandated to vaccinate them all.

There needed to be minimal harm to children to justify giving an intervention for a disease that is usually nothing more that a common cold in these age groups.

This is where the committees failed in their DUTY OF CARE.

https://dailyclout.io/report-73-pfizer-knew-what-pfizers-employees-and-contractors-knew-and-when-they-knew-it/

 

Originally posted on Dr. Flowers’ Substack.
Order Your Copy of the Pfizer Reports Paperback Book.
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chris flowers

Associate Professor of Radiology (retired), University of South Florida. Previously, Associate Professor of Radiology and Biomedical Imaging, University of California, San Francisco. Retired academic cancer radiologist, author and scientific paper reviewer for multiple radiology journals.

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#EUA #FDA #Pfizer 5.3.6 adverse events brazil CDC children clinical trial Covid vaccine drug safety fertility hearing mrna mrna vaccine post-marketing reproduction Vaccinated
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