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Thread: ⚠️WARNING⚠️ Please share so we can stop this before it begins. As of April 4th 2023 the FDA issued an Emergency Use Authorization for GOHIBIC (vilobelimab) the cousin to Remdesivir.
Do not be fooled by the bait and switch, this is just as dangerous.
Do not be fooled by the bait and switch, this is just as dangerous.
According to the document, “The Authorization follows the February 4, 2020, determination by the Secretary of Health and Human Services (HHS), as amended on March 15, 2023, that there is a public health emergency, or a significant potential for a public health emergency, that affects, or has a significant potential to affect national security or the health and security of U.S. citizens living abroad and that involves a novel (new) coronavirus. The virus, now named SARS–CoV–2, causes the illness COVID–19. On the basis of such determination, the Secretary of HHS declared on March 27, 2020, that circumstances exist justifying the authorization of emergency use of drugs and biological products during the COVID–19 pandemic, pursuant to the FD&C Act, subject to the terms of any authorization issued under that section.”
How can the basis of an emergency be declared for an emergency declared on March 27th 2020 when as you can see here, the supposed “public emergency” ended on May 11th 2023
cdc.gov/coronavirus/20…
cdc.gov/coronavirus/20…
Even the WHO declared an end to the Global “Public Health Emergency” days before the United States did
Is the FDA overstepping it’s authority to authorize the use of an unapproved potentially very dangerous drug for experimental use without an emergency being declared?
Read it for yourself here: fda.gov/medical-device…
You can see here that the drug is emergency use only.
I ask that doctors please do your homework before following this narrative. Here’s a link to this drug: go.drugbank.com/drugs/DB16416
I ask that doctors please do your homework before following this narrative. Here’s a link to this drug: go.drugbank.com/drugs/DB16416
Maybe it’s the $50 million dollars InflaRx received from the German government that encouraged the FDA to break the rules.
Do you see it yet? 👀 please share this thread 🙏🏽 we see everything they are doing and we will not allow it any longer.
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