1. Under EUA (Still In Effect) 49% of Vaxx Ingredients Can Be Changed Without FDA Approval

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  3. FDA panel recommends Johnson & Johnson vaccine for emergency use, formal authorization coming soon

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  4. 1 YEAR ANNIVERSARY OF TRUMP FORCING THE FDA TO GIVE EMERGENCY USE AUTHORIZATION TO THE PFIZER SHOT

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  5. FDA panel recommends Johnson & Johnson vaccine for emergency use, formal authorization coming soon

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  6. Dr. Robert Malone: Peter Marx & The FDA Are Committing Fraud (Includes Alt Ways To Treat COVID)

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  7. Approval versus authorization: All three vaccines still being evaluated by FDA

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  8. Dr. Nathan Thompson - Pfizer seeks FDA authorization for this in children

    Dr. Nathan Thompson - Pfizer seeks FDA authorization for this in children

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  9. FDA panel recommends Johnson & Johnson vaccine for emergency use, formal authorization coming soon

    FDA panel recommends Johnson & Johnson vaccine for emergency use, formal authorization coming soon

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  10. Pfizer seeks FDA authorization for COVID-19 vaccine for 5 to 11 year olds

    Pfizer seeks FDA authorization for COVID-19 vaccine for 5 to 11 year olds

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  11. The Kuhner Report: FDA abruptly revokes emergency use authorization for monoclonal antibodies (aired: 01/26/2022)

    The Kuhner Report: FDA abruptly revokes emergency use authorization for monoclonal antibodies (aired: 01/26/2022)

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  12. Novavax ad finally acknowledges cardiac toxicity, absence of full FDA approval

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  13. FDA gives emergency approval to Johnson & Johnson's first single-shot COVID vaccine

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  14. The potential FDA plan to inject kids 5 years and younger with abortion-tainted COVID jabs

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  15. This is why the FDA isn’t pulling authorization of the contaminated COVID jabs Dr. Janci Lindsay

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  16. Pfizer has withdrawn its application to the FDA for authorization on Covid vaccinations for kids under 5, due to not "enough data"

    Pfizer has withdrawn its application to the FDA for authorization on Covid vaccinations for kids under 5, due to not "enough data"

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  17. Pfizer Has Withdrawn Its Application To The FDA For Authorization

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