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From:Clerk of the Board
To:Mutony, Heather
Cc:Lee, Lewis
Subject:Board Correspondence - FW: Moderna mRNA flu vax - +100 deaths - 75% adverse events.
Date:Tuesday, August 25, 2026 7:33:55 AM
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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>
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Subject: Moderna mRNA flu vax - +100 deaths - 75% adverse events.
Public Record
Elizabeth Eads, DO reposted
Dr Sherri Tenpenny
@BusyDrT
What was the FDA thinking by approving the new Moderna mRNA flu vax? Over 100
deaths and ~75% adverse events? Does this sound safe to you? I talked about in this
week's Morning Coffee. Watch here: https://drtenpenny.substack.com/p/morning-coff ee-august-19-2026-edition Nic
Hulscher's epidemiology team just reanalyzed the FDA’s own data used to approve
mFLUSIVA. Here's what they found. To prevent just ONE influenza hospitalization,
5,017 people had to be vaccinated at the COST of: ~2 excess unexplained DEATHS
~278 disabling Grade 3 systemic reactions ~3,798 adverse reactions Compared with the
standard-dose flu vaccine, that amounts to approximately 1,454 ADDITIONAL adverse
reactions and 233 ADDITIONAL disabling Grade 3 systemic reactions for every
hospitalization prevented. Unexplained deaths were 2.55× more frequent among
mFLUSIVA recipients, while disabling Grade 3 systemic reactions were 6.15× more
frequent than with the standard-dose flu vaccine. Literally EVERY SINGLE solicited
adverse event was more frequent in the mFLUSIVA group. Neither pivotal trial
included a placebo arm, and no influenza-mortality endpoint was ever measured.
Moreover, mFLUSIVA commits recipients to annual lifelong exposure to nucleoside-
modified mRNA technology despite evidence of residual DNA contamination, genomic
integration, protein misfolding, proteostatic collapse, body-wide biodistribution, years-
long persistence, and compounded biological injury with repeated dosing. Our study
and accompanying information were sent directly to Secretary Kennedy and officials at
HHS, FDA, CDC, and NIH. We hope Secretary Kennedy and federal health officials
make the life-saving decision to remove this extremely hazardous product from the
market before widespread administration begins. In light of the evidence now before
them, allowing mFLUSIVA to remain approved would be a grave mistake.
https://x.com/BusyDrT/status/2090849807384613374?s=20
diana dreiss