July 28, 2021 (LifeSiteNews) — As the adverse events count related to COVID-19 vaccines continues to grow around the world, an American medical practitioner has claimed that the U.S. Food and Drug Administration (FDA) had advance notice of some of the possible severe health defects now being reported following use of the jabs, including death, before granting them “emergency use authorization” (EUA) for distribution among the general public.
Bryan Ardis, a chiropractor who has closely followed the trial, development, and public administration of COVID-19 vaccines, spoke with Brannon Howse during his live segment on Lindell TV in a June 11 interview. Ardis explained that the FDA had been presented a document detailing the potential side effects of the proposed anti-COVID jabs for monitoring as early as October 22, 2020, at least two months before the release of the first mRNA gene therapy.
The document, titled “Plans for Monitoring COVID-19 Vaccine Safety and Effectiveness,” was produced by the FDA’s Center for Biologics Evaluation and Research (CBER), the express aim of which is “to protect and promote the public health, in part by ensuring the safety and efficacy” of vaccines regulated by the FDA.
In conjunction with the Centers for Disease Control
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