The Pandemic Could Have Been Over Much Sooner—If Not for the FDA
At critical junctures, the FDA slowed vaccine development and rollout. Its decisions almost certainly cost lives.
At critical junctures, the FDA slowed vaccine development and rollout. Its decisions almost certainly cost lives.
And it's already sold out.
Subjects diagnosed with severe post-traumatic stress disorder made substantially more progress when they received MDMA rather than a placebo.
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This is the same agency that cost thousands of lives with its botched vaccine rollout.
Two recent studies show how ham-handed efforts to reduce opioid prescriptions undermine medical care.
Who could possibly have known that that would happen?
If public health scolds get their way, they will worsen the nation’s overcriminalization problem.
But only after the company jumps over more regulatory hurdles.
America's public health officials continue to undermine public health.
The decision by the CDC and FDA to pause the Johnson & Johnson vaccine was a disastrous misstep.
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The risks of blood clots are much lower than the risks of COVID-19 illness, hospitalizations, and deaths.
Yet the company is still getting stupidly scolded by public health busybodies
The role of the state is to protect rights and guard against fraud, not to prevent people from making risky choices.
Without the feds in the way, we could have rolled out at-home diagnostic testing, set up human challenge trials, approved vaccines sooner, and vaccinated Americans more quickly.
Knowledge is probably not more dangerous than alcohol, but why risk it?
Would vaccine vigilantes be justified in stealing and distributing AstraZeneca doses locked up by order of the government?
Instead of blocking food imports during a pandemic in which supply chains are strained, the FDA should allow consumers to choose food that will fill them up.
Burdensome regulations have likely cost lives.
The Reason Roundtable takes on the FDA, Andrew Cuomo, and more.
Adding a third vaccine could get America back to something resembling normal by this spring.
Wondering what "95 percent efficacy" means? I've got some good news for you.
According to a new study, one dose of the Pfizer/BioNTech vaccine is nearly as effective as two.
It's a good idea, but it should have been done much earlier.
The winners in every battle over restrictions are the people who do whatever they please without regard for government officials.
Cell-based meat cultivation is on its way.
Contemporary psychonauts are looking for insight, relief, fun, escape, and a million other things to make their lives more interesting and bearable.
We need to speed up vaccinations in order to head off the proliferation of more contagious coronavirus variants.
"Let's do the thing, which saves the most lives," says economist Alex Tabarrok: Instead of holding back second doses, use them all right away.
The Food Safety Modernization Act is all hat and no cattle.
He will count on future production to provide second doses.
Thanks to coverage at Reason and pushback from the industry, the federal government voided $14,000 fees on do-gooder craft distillers just in time for the new year.
Distilleries just learned that to cap off a brutal year, the FDA is charging them a fee normally reserved for drug manufacturing facilities.
Pandemics are like margin calls, exposing in a moment the pre-existing weakness of various positions and institutions.
It would be the best thing to do with the $22.4 billion Congress allocated for COVID-19 testing
It took 15 years for the agency to decide that consumers didn’t actually need to be protected from the threat of substandard fruit desserts.
We could double the number of Americans vaccinated against COVID-19.
FDA will likely issue an emergency use authorization for a second COVID-19 vaccine tomorrow.
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Now we wait for the FDA to get around to approving it later this week.
Don't let stories of rare and dangerous side effects discourage you from getting immunized.
Full FDA approval is likely, and vaccinations could begin next week.
Some scientists offer an important reminder about cause and effect.
It is likely to be approved for distribution by the end of the week.