Registered: Aug 2004
Location: Chattanooga, Tn
Posts: 22516

This has been FDA approved to treat Covid now. The studies show that it has a greater than 90% success rate in keeping patients from dying. You can take it at home and don't even need to be hospitalized. You take 1pill twice a day for 5 days. You have to start within 3-5 days after your first symptoms. Doesnt that sound like the panic is over? If you get Covid, you just take the pills and you are cured. Then you have natural immunity.

Now here is the problem. The government (Biden) got involved. They bought up all of the pills. If you want them, you have to get them from the government. The corrupt politicians will decide who lives and who dies. Think back to Cuomo having his family and friends vaccinated when they first came out and were in short supply. Remember when President Trump got Covid and was treated with inferon before anyone else got any? Does anyone else see this as a problem?

I can't wait to see how much Paxlovid makes it to the black market and how much it will cost? What is your life worth?

Last edited by Richard Lambert on 12-23-2021 at 03:00 PM

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Registered: Aug 2004
Location: Chattanooga, Tn
Posts: 22516

Guess what the Biden administration is focusing on....Covid testing kits. Will tests cure Covid? Biden has enacted the war powers act and promised to finance test kit producers and streamlined delivery of government test kits.

What is wrong with this picture... more pills that cure Covid or tests that only tell you that you have it. Are they that stupid? Or corrupt and getting kickbacks from test kit manufacturers?

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Registered: Dec 2019
Location: Everywhere
Posts: 1058

Bye Bye EAU PCR tests....
Their accuracy has been questioned as to being inaccurate detecting COVID from the beginning
Now it is a done deal

After December 31, 2021, CDC will withdraw the request to the U.S. Food and Drug Administration (FDA) for Emergency Use Authorization (EUA) of the CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel, the assay first introduced in February 2020 for detection of SARS-CoV-2 only. CDC is providing this advance notice for clinical laboratories to have adequate time to select and implement one of the many FDA-authorized alternatives.

CDC encourages laboratories to consider adoption of a multiplexed method that can facilitate detection and differentiation of SARS-CoV-2 and influenza viruses. Something we foil hat wearers have been arguing all along

https://www.cdc.gov/csels/dls/locs/..._Testing_1.html

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