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FDA approved the injection for seniors before any clinical benefit was shown, and before confirming vaccinated can't shed vaccine components onto unvaccinated, raising informed consent concerns.
Yesterday, Moderna, Inc. announced that the U.S. Food and Drug Administration (FDA) has "approved mFLUSIVA® (mRNA-1010), a new vaccine against seasonal influenza, for use in all adults 50 years and older."
Even though the alleged benefit for adults 65 and older was never proven.
The move comes after the FDA's Vaccines and Related Biological Products Advisory Committee (VRBPAC) voted unanimously in June that the "benefits" of Moderna's experimental mRNA influenza vaccine "outweigh its risks."
It also comes after President Trump selected a military-grade influenza pandemic architect, Erica Schwartz, to run the CDC.
Moderna expects to have the drug available for eligible populations in the U.S. for the 2026-2027 respiratory virus season.