FDA Trying to Rewrite COVID History on Prohibiting Ivermectin, Dr. Atlas Says
Boyden Gray & Associates filed a lawsuit in June on behalf of three doctors who allege that the U.S. Food and Drug Administration (FDA) illegally interfered with their doctor–patient relationships, resulting in harm. They also claim that the FDA broke the law when the agency issued statements prohibiting the use of ivermectin to treat COVID-19.
In response to the lawsuit, lawyers for the FDA claimed that its guidance for people to “stop” taking ivermectin for COVID-19 was informal and just a recommendation; as such, they weren’t mandating against it.
However, in an interview that aired on NTD’s “Newsmakers” on Nov. 23, Dr. Scott Atlas, a senior fellow in health care policy at the Hoover Institution at Stanford University, confirmed that the FDA did, indeed, take an “unprecedented” approach against ivermectin and said that their defense amounts to the FDA trying to rewrite COVID-19 history. (See link for article and video)
“What we’re seeing is a complete Orwellian rewrite of all kinds of things during this pandemic,” Atlas told NTD. “Many colleagues of mine were always saying the truth will prevail. And once the truth comes out, that some of these drugs were either useful or safe … there’s a lot of ‘cover your behind.’”
And no wonder they are covering their tracks….
Project Veritas has obtained startling never-before-seen documents regarding the origins of COVID-19, gain of function research, vaccines, potential treatments which have been suppressed, and the government’s effort to conceal all of this.
The documents in question stem from a report at the Defense Advanced Research Projects Agency, better known as DARPA, which were hidden in a top secret shared drive.
Project Veritas has obtained a separate report to the Inspector General of the Department of Defense written by U.S. Marine Corp Major, Joseph Murphy, a former DARPA Fellow.
The information relating to IVM and HCQ are found on page 4 of a document whose subject is, “SARS-CoV-2 ORIGINS INVESTIGATION WITH US GOVERNMENT PROGRAM. UNDISCLOSED DOCUMENT ANALYSIS” (emphasis in original) and which is dated August 13 2021. The relevant portion reads (note that the coronavirus is called “SARSr-CoV-WIV” in the document):
Because of its (now) known nature, the SARSr-CoV-WIV’s illness is readily resolved with early treatment that inhibits the viral replication which spread the spike proteins around the body (which induce a harmful overactive immune response as the body tries to clear the spikes from the ACE2 receptors). Many of the early treatment protocols ignored by the authorities work because they inhibit viral replication or modulate the immune response to the spike proteins, which makes sense within the context of what EcoHealth was creating. Some of these treatment protocols also inhibit the action of the engineered spike protein. For instance, Ivermectin (identified as curative in April 2020) works throughout all phases of the illness because it both inhibits viral replication and modulates the immune response. Of note, chloroquine phosphate (Hydroxychloroquine, identified April 2020 as curative) is identified in the proposal as a SARSr-CoV inhibitor, as is interferon (identified May 2020 as curative). [Emphasis added.]