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FDA downplays COVID vax overdosing as hydroxychloroquine shows more promise in European research

Agency portrayed ivermectin as dangerous by conflating human and livestock dosages, but didn’t take pains to warn providers Moderna jabs have “notably more” than authorized for kids.

The FDA repeatedly told the public that an antiviral with a sterling safety record, ivermectin, should not be used to treat COVID-19 because it was also prescribed, at higher dosages, to livestock.

The agency didn’t appear to show the same concern about correctly dosing the new single-shot mRNA COVID vaccines and is now scrambling to educate healthcare providers not to give children adult-strength jabs even while denying that overdosing is a safety risk.

Its demonization of cheap, widely available antivirals to treat SARS-CoV-2 infections in higher-risk populations looks increasingly shortsighted, with two new peer-reviewed studies on hydroxychloroquine’s effectiveness when combined with azithromycin, a common antibiotic.

The Food and Drug Administration yanked emergency use authorization from HCQ in summer 2020 despite The Lancet retracting a study three weeks earlier that linked the antiviral to a higher risk of death from COVID, saying the authors could not “vouch for the veracity” of their data sources.

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3 thoughts on “FDA downplays COVID vax overdosing as hydroxychloroquine shows more promise in European research”

  1. Oh, how I begged my doctor for hydroxycloroquine when I had covid and nearly died. He said “NO, it doesn’t help:”!!! He and I both knew that was BS!!! It does help!!! Doctors were not allowed to give it because it did work!!!!! They wanted people to die. Thin the herd!! Depopulate!!! So, if you get covid, tell your doctor you want and need HYDROXYCLOROQUINE!!! It does work!

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