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Shoot To Kill: FDA Quietly Updates Emergency Authorization Use Of Novavax Vaccine Despite Deadly Side Effects And No Current Public Health Emergency

FDA seems to have stopped caring about drugs being ‘safe and effective’

Gateway Pundit

(Gateway Pundit) Late last month, The Gateway Pundit reported that Joe Biden’s regime will once again begin to offer “at-home” COVID test kits again after stopping the taxpayer-funded distribution on June 1, 2023.  Each family can now receive up to four free tests per person after Biden spent $600 million to acquire 200 million tests.

Yesterday, amidst the frenzy over the removal of Kevin McCarthy as Speaker of the House, the Food and Drug Administration amended the Emergency Use Authorization (EUA) for the Novavax COVID-19 “vaccine” despite the Public Health Emergency officially ending almost five months earlier on May 11, 2023, according to the CDC.  So how is the FDA seemingly able to approve an Emergency Use Authorization when, according to the CDC, there is no longer an emergency?  A letter published to FDA.gov states that:

 

Meanwhile, as more and more data becomes available since the release of the “vaccines”, many health professionals are calling into question things like “turbo cancers“, sudden rises in excess mortality and mysterious white fibrous clots being found in “50% of cadavers” by travel embalmer, Richard Hirschman:

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