(Total Views: 639)
Posted On: 05/28/2020 3:22:34 PM
Post# of 148984
The only bad thing happening is FDA making CYDY jump through hoops with leronlimab. This as opposed to their treatment of HCQ....what was it...90k patient samples for those in charge to finally declare that HCQ has no efficicy?!? Why 90k to confirm something doesn't work unless you really really really want it to work?
What is more acceptable to the public eye? Subjecting 90k people to harmful side effects trying to prove something works but failing to do so or giving EUA on a sample of ~110 (60 EIND + 50 from trial) and continuing trials?? Mind boggling.
All I am saying is that EUA should be given. That means leronlimab will be given UPON request for emergency cases without having to go thru the cumbersome process for EIND use.
100k people dead now in the US and growing. I expect this number will rise significantly based on the photos I've seen of people celebrating this past weekend.
What is more acceptable to the public eye? Subjecting 90k people to harmful side effects trying to prove something works but failing to do so or giving EUA on a sample of ~110 (60 EIND + 50 from trial) and continuing trials?? Mind boggling.
All I am saying is that EUA should be given. That means leronlimab will be given UPON request for emergency cases without having to go thru the cumbersome process for EIND use.
100k people dead now in the US and growing. I expect this number will rise significantly based on the photos I've seen of people celebrating this past weekend.
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