this post was submitted on 05 Jun 2025
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Over the last several decades, the Food and Drug Administration has allowed pharma companies to sell hundreds of drugs to patients without adequate evidence that they work and, in many cases, with clear signs that they pose a risk of serious harm.

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[–] rodneyck@lemmy.world 17 points 1 day ago

It is almost as if ...hmmmm...they are working for the very people they regulate? Say it isn't so. 🤔

[–] cupcakezealot@lemmy.blahaj.zone 33 points 1 day ago (1 children)

and yet puberty blockers should be banned despite being tested with no ill effects for thirty years

[–] burgerpocalyse@lemmy.world 6 points 1 day ago

the problem with puberty blockers is that they have an explicit and verifiable use case. thats not what drugs are supposed to do! theyre supposed to do whatever you say they do!

[–] l_isqof@lemmy.world 8 points 1 day ago

Yeah, didn't one of 'em dickheads recently say we all have to die somehow... this is just one other way.

[–] Neuromancer49@midwest.social 107 points 2 days ago (5 children)

The article brings up some great points, some of which that I, an industry insider, weren't even aware of, especially the historical context surrounding the AIDS epidemic. I'll jump into the thread to critique an issue within the article.

One of the four pillars recommended by the FDA (control groups) are great in theory but can lead to very real problems in practice, specifically within indications that have an unmet treatment need or are exceptionally rare conditions.

If you have a disease that is 99% fatal but has 0 standard of care treatment options, is it ethical to ask a participant to enroll in a clinical trial and potentially not receive the study treatment/be on placebo? Or, what if the trial involves an incredibly invasive procedure like brain surgery - is it ethical for people to do a placebo procedure? Food for thought - and an explanation for why so few trials meet all four criteria proposed by the FDA.

Happy to answer questions about the industry if anyone has them.

[–] Bluewing@discuss.online 9 points 1 day ago

Medicine has always relied on killing enough patients to determine how safe/effective or not a drug or procedure might be. We simply do not have the technology to provide definitive answers any other way as of yet. This is why one "practices" medicine and not "does" medicine. And administering a drug to a patient is called a "trial." There is simply no way to know the outcome until the outcome arrives. Years of experience can give you a fair indication of what to expect, but expectations are not definitive answers.

As a keynote speaker ER Doctor stated at an EMS seminar I attended, "No matter how much knowledge and skills we think we know and have, modern medicine still boils down to doing things to keep the patient amused and letting nature take it's course." As a simple medic, that was a thought that stuck with me through my 15 years in the back of the bus. It scared the bejeezus out of me.

[–] ClockworkOtter@lemmy.world 25 points 2 days ago (1 children)

When it comes to therapies that are likely toxic, e.g. chemo, that's why the sponsor has to demonstrate through pre-clinical data that there is a high enough likelihood that the benefits will outweigh the harm that it is a legitimate therapy to trial on humans. Even then there should still be thorough, audited processes for obtaining fully informed consent before recruiting patients into these trials, including making certain they are aware the trial may cause more harm than standard of care.

It's the burden of evidence required in pre-clinical data that makes me defend animal testing despite being vegan.

[–] Neuromancer49@midwest.social 14 points 1 day ago (1 children)

The consent process for clinical trials has a ton of guidance (ICH GCP), but the onus is on the clinical monitors and hospitals to make sure it's done correctly. Many trials now generate supporting documentation in which hospital staff are required to describe the circumstances in which consent was acquired. If the documents are generated, then it's auditable.

Things get a bit hairy when you look at trials in Alzheimer's and other cognitive disorders, because the patient may not be coherent enough to withdraw from the trial. In those cases, a legal guardian is responsible for the decision.

[–] ClockworkOtter@lemmy.world 6 points 1 day ago (1 children)

Yes, though if the sponsor is doing it on the cheap then they might pick facilities and monitors who don't care or don't have the capacity to pick up on all the details, or scrutinise minutiae. The monitor can only QC what's written down for example, and an investigator can be perfectly capable of having the bare minimum of a consent process and copy pasta as if it was done thoroughly.

I'm glad all my participants are of sound mind; the idea of navigating the world of incapacity and research gives me the heebie jeebies.

[–] Neuromancer49@midwest.social 5 points 1 day ago (1 children)

Good point, I'm assuming all monitors are as good as mine.

[–] ClockworkOtter@lemmy.world 2 points 1 day ago

I wish all mine were as good as the best I've had.

[–] captainlezbian@lemmy.world 14 points 1 day ago

Unless you actually start looking into the whole of the aids epidemic its easy to miss what an absolute clusterfuck it was. The systems in place weren't prepared at all for it and through a combination of maliciousness, ideological hardheadedness, and novel circumstances more Americans were killed by a virus than by the Viet Cong. But because it hit a group that was already fighting for our rights as well as the fact physicians in high places understood that their duty was not to the public "morality" but to public health things were able to be fought.

[–] altphoto@lemmy.today 7 points 2 days ago (1 children)

Opening someone's head to pretend to have done something sounds very unnecessarily cruel and stupid.

[–] webghost0101@sopuli.xyz 23 points 2 days ago (2 children)

Thats their point. How do you test placebo effect for a surgical operation?

[–] bss03@infosec.pub 2 points 1 day ago* (last edited 1 day ago) (1 children)

You can do single-blind. You do prep, anesthetize, then open the card that decides if the surgery continues, or if the patient is simply awakened at the expected time.

You can also do it for surgeries that use locals, but then the surgical staff has to do a lot of miming/acting instead of actual cutting.

Medlife Crisis did a couple of Placebo effect videos, and mentioned that he participated in a single-blind stent study.

I don't know how you'd do double-blind.

[–] webghost0101@sopuli.xyz 2 points 1 day ago

That a great take.

Double blind could be a different team comes In and either does the surgery or fakes it. And this team also does or Fakes the after care.

This team is never to communicate with patient or normal staff.

[–] ToastedRavioli@midwest.social 5 points 2 days ago* (last edited 2 days ago) (1 children)

Either way, that is a pretty massive digression from the article, which is about medications. Apparently more people are dying on average from recently approved drugs than are dying from all illegal drug use combined. And the examples are not for extremely rare medications

“We need an agency that’s independent from the industry it regulates and that uses high-quality science to assess the safety and efficacy of new drugs,”… “Without that, we might as well go back to the days of snake oil and patent medicines.”

We basically are already there now, it seems

[–] Neuromancer49@midwest.social 11 points 1 day ago

Fair point, but a lot of the article talks about how many studies aren't meeting all four pillars of clinical trial design - that's where my issue comes in, I think reporting that X% of trials do not meet all pillars is a bad metric.

And, not all medications these days are pills or IV infusions - some medications and treatments, which are governed by the FDA, are more invasive and more complicated.

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[–] billiam0202@lemmy.world 66 points 2 days ago (1 children)

Phenylephrine is back on the menu, boys!

[–] AbidanYre@lemmy.world 29 points 2 days ago (7 children)

That's the best case.

I'm thinking thalidomide.

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[–] mienshao@lemm.ee 45 points 2 days ago (2 children)

Not arguing against the substance of the article, but I can’t help but wonder if this is the best way to address this issue. Measles was eradicated from the US but is now back and has claimed lives purely due to vaccine skepticism. I just worry that yet another article criticizing the FDA for pushing drugs that aren’t safe/effective will do more harm than good at this point. Idk, I just sincerely question if now is the time to give americans more reasons not to trust medical professionals. (Again, not arguing with the substance of the article—very disappointing and disturbing that FDA is doing this—but just concerned about the time, manner, and place of this criticism.)

[–] brucethemoose@lemmy.world 34 points 2 days ago* (last edited 2 days ago) (14 children)

Both can be true.

It can be true that the FDA was corrupted/captured to some extent and needs more 'skeptial' and less-industry-friendly leadership. At the same time, skepticism in science is not the answer.

This is my dillema with MAGA. Many of the issues they tackle are spot on, even if people don't like to hear that. They're often right, even when the proposed solutions are wrong and damaging. I think this a lot when I hear RFK speak, nodding my head at the first assertion then grinding my teeth as he goes on.

[–] SnotFlickerman@lemmy.blahaj.zone 18 points 2 days ago* (last edited 2 days ago) (1 children)

This is such an important thing to note. The MAGA set aren't completely oblivious. It's the same issue with how they don't trust "mainstream media," the problem doesn't lie in accepting that media must be viewed with skepticism and critical thinking, the problem lies with the critical thinking ending at "I can't trust the mainstream media."

What the MAGAs are actually practicing is cynicism not skepticism. They have thrown the baby out with the bathwater. Because they have realized some sources aren't always entirely trustworthy, they stop trusting them entirely and instead listen to random jackholes on the internet. It's actually an abdication of critical thinking. Just flat out rejection instead of reading with a critical eye and skeptical mind.

[–] taladar@sh.itjust.works 1 points 1 day ago

They also don't apply the same attitude to those random sources they use instead. That is really the biggest problem with their approach. Literally going "you can't trust anyone any more" would be better than what they do.

[–] thesohoriots@lemmy.world 9 points 2 days ago

Yeah that’s absolutely how they lure people in. Sensible issues to be concerned about, starts out normal, then about two links of thought in, the tinfoil hats come out and the solution is fucking nuts.

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[–] darkstar@sh.itjust.works 6 points 1 day ago

Hmmm, now where have I heard this before?...

[–] por_que_pine@lemm.ee 15 points 2 days ago (1 children)

Sell drug, make money, bribe officials, repeat....Seems like it works fine, for big pharma.

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[–] trailee@sh.itjust.works 18 points 2 days ago (2 children)

American health insurance companies are famously miserly, and this seems like a great area to use penny pinching for good. Where the hell are the insurance CFOs who should be demanding efficacy proof instead of being swindled along with the masses?

[–] AbouBenAdhem@lemmy.world 18 points 2 days ago

They’re busy researching new and exciting ways of denying coverage.

[–] ragebutt@lemmy.dbzer0.com 10 points 2 days ago (1 children)

They absolutely do this. A drug with a lack of efficacy data is a great way to get shortlisted to insurance denials

It’s one of the frustrating things bc people can then easily manipulate the issue. A drug that can be prescribed a doctor and filled by a pharmacy being denied by an insurance company is very easy to write about online. Then it’s a slam piece, “x insurance company denied me my meds”. Basically 0 people will have any interest in the nuance that the medication is bullshit or possibly even harmful. Too bad insurance companies made their bed by being absolutely horrible for decades, I guess.

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[–] BitterChocolate@lemmy.zip 6 points 2 days ago

Since "evidence based medicine" has been a corrupt joke for many decades now, why be surprised now? As long as people continue to claim that real science - which assumes and even demands skepticism and testing and trial and even disagreement as a never-ending process that works for real results and continued improvement - is somehow "anti-science", there is no limit to how whacked "medication" or "treatment" can be or become.

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