Mon Feb 7, 2022 – 12:56 pm EST
WASHINGTON (LifeSiteNews) — The U.S. Food and Drug Administration (FDA) has restored a document to its website which reports that the rate of heart inflammation among young men after receiving the experimental COVID-19 jabs is far higher than previously understood.
The move comes after the 30-page document, which outlines the reasons the FDA granted full approval for Moderna’s “Spikevax” COVID-19 mRNA drugs on January 31, was abruptly removed from the agency’s website without explanation just hours after conservative news organization The Epoch Times reached out to the FDA for questions about the data.
So, the FDA apparently removes from its website the document explaining why it approved the Modena vaccine. I really wonder why …https://t.co/PeAoUI2cSd
— JayKayYes 🍀 (@JayKayYes) February 6, 2022
The initial removal of the document had sparked backlash from members of congress, the National Vaccine Information Center, and journalists, who have argued that the FDA’s actions failed to uphold standards of transparency.
According to The Epoch Times, the document, entitled the Summary Basis for Regulatory Action (SBRA), was made public on February 1, a day after the FDA granted approval for the Moderna jabs.
The remainder of this article is available in its entirety at LifeSite News
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