More than 600,000 people in Tricare, a health care program of the United States Department of Defense Military Health System, received emails July 17 asking if they would donate blood for research as "survivors of COVID-19."
But just 31,000 people affiliated with the U.S. military have been officially diagnosed with the coronavirus, which prompted confusion, Military.com reported last week.
"Just wondering [if] anybody [got] an email from Tricare saying since you are a COVID survivor, please donate your plasma.?? I have NOT been tested," wrote a beneficiary on Facebook. "Just remember all those people inputting data are human and make mistakes."
The mass email went to every beneficiary located near a collection point.
(Score: 2) by JoeMerchant on Thursday July 30 2020, @11:44PM (3 children)
The credo is: safe and effective.
First, do no harm. Demonstrate that your drug, device, whatever is safe to use. In the event that it is not completely safe, then the burden is to demonstrate that the potential harm is outweighed by the expected benefits.
Effective: does the drug, device, whatever do what is claimed better than placebo? Placebo is a pretty high bar, just paying attention to someone's problem is often enough to fix it, but we really don't need more placebos on the market charging money for what could be accomplished with a decent bedside manner.
You think anything that is regulated "slowed down" by the FDA is actually going to reach and positively impact even 10% of the people on this planet? You must have been smoking with Elon.
🌻🌻 [google.com]
(Score: 1) by khallow on Friday July 31 2020, @01:43PM (2 children)
There we are. No one sees the harm of opportunity cost. Everyone sees the harm from a few people dying from a bad drug.
Much closer to 100% than that. By the end of this century, I think most people no matter where they are in the world will be part of the developed world and have access to advanced medical technology. Thus, the amount of time the FDA obstructs medical progress by "doing no harm" means their lives in the future will be a little bit poorer and shorter lived.
(Score: 2) by JoeMerchant on Friday July 31 2020, @02:06PM (1 child)
In most cases, no one knows the value of opportunity. There's speculation, hope, guesses, estimates, but you don't really know the future.
Most of this "advanced medical technology" you are concerned with bringing to the broader masses is a bunch of over-complicated, over-priced, "value creation" that could and should be boiled down to the essence of what it does to improve patients health/quality of life, but instead is being developed to extract ever-more profit out of the sick. The "free market" is doing little or nothing to steer product development toward patient benefit.
Go find Kurzweil and do some meditative yoga while you extrapolate simple concepts into utopian images of the future. Better hurry, he's going to miss the singularity by a wide margin, and so are you.
🌻🌻 [google.com]
(Score: 1) by khallow on Friday July 31 2020, @11:06PM
Doesn't mean that opportunity costs should be ignored just because "no one knows". And you follow it up with
Why rhetorically invoke the "free market" when the FDA makes it very non-free? I'll note a second, more recent post from a different story where you non-sarcastically observe [soylentnews.org]:
In the big picture, 1 million premature deaths a few times a century or millennium from bad medical technology, while scary when it happens, isn't as worthwhile to address as the irreversible development of better medical technology. The FDA enables the non-free market in medical technology where obvious medical advances like your "virtual cure for bulimia" can be ignored in preference to "over-complicated, over-priced, 'value creation'". They're the gate keepers that keep out ideas with too low a ROI, the barrier to entry for new advances that would upset the status quo and make our lives better.