“FDA’s war on public health is about to end,” Kennedy wrote. “This includes its aggressive suppression of psychedelics, peptides, stem cells, raw milk, hyperbaric therapies, chelating compounds, ivermectin, hydroxychloroquine, vitamins, clean foods, sunshine, exercise, nutraceuticals and anything else that advances human health and can’t be patented by Pharma."
Anyone know what chelating compounds he is talking about?
He mentions clean foods, but the Trump EPA is protecting corporations from regulations more than its protecting citizens from pollution.
The raw milk thing is funny to me in a semi-morbid way i guess, i find it for sale all over the place and more expensive then just regular, even organic, whole milk. Pasteurization doesn't seem to be some evil ultra-processing of milk, it just kills bacteria that can make you sick. There's no preservative or other additives that i'm aware of. Pasteurization just doesn't seem like something anyone would get worked up about but here we are.
Reading "Bottle of Lies" by Katherine Eban, I'd argue that the collapse of the FDA was well underway before the current administration. The FDA was completely unable to regulate overseas drug manufacturers, resulting in many, many problems. Sincere attempts to inspect overseas drug makers with random inspections universally results in shutdowns, which cause politically unpopular drug shortages, making enforcement politically difficult.
I wish someone would convince RFK that prescription drug ads are bad for his brand of quack medicine. We could at least get rid of that societal cancer while the rest is torn down.
Why are prescription drug ads bad? Its not like consumers can prescribe or buy it for themselves.
If there is a problem with overconsumption or misuse of prescription drugs isn't the blame on the medical professionals that prescribe them? Ads to the general public seems far down on the list of culprits here.
Worth reminding everyone that, on top of pharma and food, the FDA also regulates medical devices.
Insufficient regulation both on approval _and_ inspection of medical devices (thinking surgical applications and implantables for example) is as impactful on patient safety as drugs.
I used to work for that branch. They'd joke it's the FDDA. Paid peanuts but I learned a lot and had a great boss (who showed up to my house one day unannounced to gift me the Art of Programming because I said I didn't have a copy months prior).
There are serious cyber security implications too.
A recent discovery was a heart rate monitor used in hospitals that sent all data, including full patient details, to Chinese servers, and would accept arbitrary code updates from said servers.
If you wanted to kill a diplomat, muting or spoofing heart rate data while they have a cardiac event in hospital would be a very sneaky way to do it.
i know this is a very political thing now but i've had friends (smart phd people who work industry) very annoyed at the fda for many years, and maybe this collapse is good!
the fda started with a noble mission but they've been getting heavy handed. or better cliched - slow handed with getting things certified.
you can solve this one or two ways: drop regulation or increase staffing.
so many institutions have unnecessary fluff, tremendous red tape (why do i need environmental review to stick a shed in my backyard??), our modern lives have too much regulation.
let's hope for the best.
the old system is holding back drugs.. there should have been more ozempics, more breakthroughs had the fda not been so slow. companies have a strong incentive not release bad drugs now.. lawyers are not cheap and law firms know money can be made.. it's not the 1930s anymore.. (okay it's still the 1930s in certain places of the world, that's a criticism)
typing this out hoping to convince any regulation reduction is good reduction, i thought of a third fda option: the fda let's everyone go hog wild initially but looks at the top consumed products and checks them for safety and efficacy each year.
The FDA's creation was directly triggered by multiple mass poisoning incidents in the early 1900s.In 1937 over 100 people died from diethylene glycol-contaminated medicine, leading to the 1938 Food, Drug, and Cosmetic Act that significantly expanded FDA authority.
And if they had stuck with making sure medicine sold is exactly what it says on the bottle instead of expanding to telling me which medications I am allowed to have, I would be their biggest supporter.
Vinay Prasad, the new FDA chief medical and scientific director, is an extremely sensible guy and a co-author of a great 2013 book on evidence-based medicine targeting the lay audience (Ending Medical Reversal)
The NYT article presents his COVID vaccine policy changes as yet more crazy MAGA shit, whereas in fact he holds nuanced views, based on up-to-date review of available evidence. He has published in NEJM and elsewhere on the topic:
Destruction precedes creation. Things have ossified to the point where change seems impossible. While I think the way we’ve gone about it is absurd, I can still hope that something better will replace it.
The one thing I liked about RFK is that he was going to "take on" the big food conglomerates and all the garbage that they are feeding Americans especially those unable to afford, or who do not have easy access to, healthy alternatives (whereas the garbage food is ubiquitous).
It would seem dismantling the FDA is the opposite of that; what's needed are more regulations on food, or at least policies that result in more healthy food being available and affordable to Americans, not less regulation.
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[ 3.0 ms ] story [ 47.7 ms ] threadAnyone know what chelating compounds he is talking about?
He mentions clean foods, but the Trump EPA is protecting corporations from regulations more than its protecting citizens from pollution.
I would wager cardiac and arterial disease would plummet.
If there is a problem with overconsumption or misuse of prescription drugs isn't the blame on the medical professionals that prescribe them? Ads to the general public seems far down on the list of culprits here.
Insufficient regulation both on approval _and_ inspection of medical devices (thinking surgical applications and implantables for example) is as impactful on patient safety as drugs.
A recent discovery was a heart rate monitor used in hospitals that sent all data, including full patient details, to Chinese servers, and would accept arbitrary code updates from said servers.
If you wanted to kill a diplomat, muting or spoofing heart rate data while they have a cardiac event in hospital would be a very sneaky way to do it.
Pity the old ways are
> You’ve died of dysentery
the fda started with a noble mission but they've been getting heavy handed. or better cliched - slow handed with getting things certified.
you can solve this one or two ways: drop regulation or increase staffing.
so many institutions have unnecessary fluff, tremendous red tape (why do i need environmental review to stick a shed in my backyard??), our modern lives have too much regulation.
let's hope for the best.
the old system is holding back drugs.. there should have been more ozempics, more breakthroughs had the fda not been so slow. companies have a strong incentive not release bad drugs now.. lawyers are not cheap and law firms know money can be made.. it's not the 1930s anymore.. (okay it's still the 1930s in certain places of the world, that's a criticism)
typing this out hoping to convince any regulation reduction is good reduction, i thought of a third fda option: the fda let's everyone go hog wild initially but looks at the top consumed products and checks them for safety and efficacy each year.
I get annoyed by web development, but I wouldn't want to see the solution be a federally mandated burning to the ground of the HTML standard.
Here's an EconTalk podcast with the other co-author, Adam Cifu, talking about the book. https://www.econtalk.org/adam-cifu-on-ending-medical-reversa...
The NYT article presents his COVID vaccine policy changes as yet more crazy MAGA shit, whereas in fact he holds nuanced views, based on up-to-date review of available evidence. He has published in NEJM and elsewhere on the topic:
https://www.nejm.org/doi/full/10.1056/NEJMsb2506929
A short take on the above from Adam Cifu, whom I respect greatly: https://www.sensible-med.com/p/prasad-makary-and-an-evidence...
With all of that, I suspect that the rumours of FDA's death are greatly exaggerated.
It would seem dismantling the FDA is the opposite of that; what's needed are more regulations on food, or at least policies that result in more healthy food being available and affordable to Americans, not less regulation.