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From:Clerk of the Board
To:Mutony, Heather
Cc:Lee, Lewis
Subject:Board Correspondence - FW: EUA invalid. Had therapeutics.
Date:Thursday, September 24, 2026 1:29:05 PM
Attachments:image001.png
Please see Board Correspondence -
Lewis LeeAdministrative Technician - ConfidentialButte County Administration25 County Center Drive, Suite 200 • Oroville, CA 95965T: 530.552.3326www.buttecounty.ca.gov | lelee@buttecounty.ca.gov
From: lance dreiss <lancedreiss@att.net>
Sent: Thursday, September 24, 2026 10:04 AM
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Subject: EUA invalid. Had therapeutics.
Dr Sherri Tenpenny
@BusyDrT
In Fauci's diary, on March 18, 2020, he noted a discussion with the Oval Office about using hydroxychloroquine. President Trump had heard anecdotal reports that it worked and wanted to make it available to Americans. HHS Secretary Alex Azar said America had millions of doses stockpiled and that he could approve hydroxychloroquine immediately. But Fauci said no. Instead, he proposed an expanded-access protocol for hydroxychloroquine. It was already an FDA-approved drug, but Fauci wanted to study its effectiveness in this particular situation; patients could receive the drug but researchers would simultaneously study whether they actually worked. Trump agreed. The hydroxychloroquine was made available, but interestingly, Fauci asked to delay the announcement until the following day. Is this because he had to coordinate something? Later that same afternoon of March 18, Fauci sent an email to Robert Redfield, Stephen Hahn and Deborah Birx. In it, he distinguished between the two drugs: he said remdesivir should be subject to a much stricter protocol, whereas hydroxychloroquine was already approved and had extensive prior human use, but he was concerned about some of the adverse events. His email said nothing about the adverse events of remdesivir, like kidney failure. Keep in mind how horrific remdesivir was in an earlier Ebola trial. They knew about the kidney failure, and the death. On March 28, the FDA issued an EUA allowing hydroxychloroquine from the Strategic National Stockpile to be distributed to public-health authorities for certain hospitalized COVID-19 patients when a clinical trial wasn't available or feasible. The federal government subsequently did distribute 31 million hydroxychloroquine tablets and left 63 million in the stockpile. The EUA was requested by BARDA, not by Fauci! But then, on June 15, the FDA revoked the hydroxychloroquine EUA after reviewing the accumulated evidence—only 2.5 MONTHS of it. They concluded that hydroxychloroquine was unlikely to benefit hospitalized COVID patients and that serious cardiac risks changed the risk-benefit assessment. Six months later, on December 11, the EUA was granted for the Pfizer vaccine. Seven days later, on December 18, the Moderna vaccine received EUA. What is interesting timing is this: Thousands of people were enrolled for the Pfizer trial beginning July 27, 2020. So they only tried HCQ for ~2 months, but the Pfizer trial ran more than 2x longer, but we now know they hid the adverse events. When will these culprits be held accountable? I have soooo many examples of Big Pharma corruption in my Zero Accountability book. If you don't yet have your copy, you can pick one up here: drtenpenny.com/zero
https://x.com/BusyDrT/status/2103152858548121877
diana dreiss