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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.
The government has been given the data. It now has the responsibility to ACT.
@SecKennedy
https://x.com/NicHulscher/status/2092033446847656444

Nicolas Hulscher, MPH @NicHulscher - The McCullough Foundation is producing a series of documentary films exposing the stunning malfeasance of our public health authorities.
Please support our work and help us fulfill our mission to ensure our government NEVER AGAIN commits such acts of tyranny and abuse against “We the People.”
https://mcculloughfnd.org/
https://x.com/NicHulscher/status/2091973644545118452