Thread by @CarlingtonRacki

Thanks to @TheLastRefuge2 for pointing out the Obama admin lifted the block on Gain-of-Function research on 1/9/17. It also only 4 days later (1/13/17) they updated the guidance on FDA Emergency Use Approval (EUA) for Medical Products during a pandemic.

federalregister.gov/documents/2017…

This EUA paved the way for the introduction of the Moderna and BioNTech (Pfizer) Covid vaccines since they never received actual FDA approval. But the EUA regulation has a caveat:
"There are no adequate, approved, and available alternatives".

This means that there are no other medications or procedures already available to treat Covid, including already approved generic drugs.

On 12/8/20, Dr @PierreKory gave detailed testimony to the US Senate Homeland Security committee on the on the high efficacy of a generic drug

called Ivermectin. All the Dems walked out of the hearing before Dr. Kory even spoke, with ranking member Gary Peters (MI) calling him a politician. Dr. Kory provided the committee with numerous studies on the effectiveness of Ivermectin, plus access to his group's research.

The video of Dr. Kory's testimony to the US Senate was removed by YouTube, of course, because it didn't conform with the WHO's orthodoxy. But the video is still up on his group's website for people to view.

covid19criticalcare.com

What is critical to note here is that only 3 days after Dr. Kory's testimony, BioNTech (with Pfizer as contract manufacturer) received the first FDA EUA for a Covid-19 vaccine on 12/11/20.

cnbc.com/2020/12/11/pfi…

Dr. Kory's group research had vast research on the efficacy of Ivermectin by October 2020, including it's high effectiveness as a prophylaxis. Meaning taking Ivermectin as a precautionary drug keeps people from contracting Covid-19, exactly what a vaccine is supposed to do.

But unlike the Covid mRNA vaccines, Ivermectin is much much cheaper, has been FDA approved and used for 40 years, and has significantly less side effects and risks.

Now this causes a big problem for the Pharma & Biotech companies that sunk many millions of $ in Covid research

because if Ivermectin was recognized by the FDA/CDC as an effective existing Covid treatment, then the new vaccines could not obtain the FDA EUA and be distributed to the world and make these companies many billions of $.

This would explain the significant push back against

Ivermectin and other generic drug like Hydroxychloroquine & Zinc. These treatments would remove the FDA EUA and eliminate the use of mRNA vaccines that have made people billions because they would then need to go through the full FDA approval process.

But even more, the vaccines are not even needed because Ivermectin, used as a prophylaxis, basically acts as a vaccine for Covid-19, as well as for treating patients with already severe Covid-19 illness.

Unfortunately with millions of people already convinced to be vaccinated, under false pretense, with the much riskier mRNA vaccines from BioNTech & Moderna, plus many governments around the world looking to increase their control over people by implementing "Vaccine Passports",

Ivermectin and other effective generics will never be widely accepted as the significant treatment for Covid-19 that they really are. Most people already vaccinated would not even want to believe it because it would make them question their own judgement. END.