Really not sure how to feel about this part lol, I mean I get it, but at the same time this is very ugh.
Really not sure how to feel about this part lol, I mean I get it, but at the same time this is very ugh.
If you remove the flag (pain), harm will continue.
I worry a lot about aging, and I'm also afraid of things like tumors or cancers that I might not feel until it's too late. As an example, I can't feel cavities forming and I didn't even notice my wisdom teeth piercing through my gums when I was a teen.
Many years later we found that the actual cause was a Cerebrospinal Fluid (CSF) Leak.
After two failed surgeries to fix it, she had enough and checked herself out.
See our documentary Pain Warriors for the whole saga.
That said, the article may not be fairly representing what happened in the first place, so...
Clicking "FDA" in the bit you quoted above takes you to a different page wherein the FDA laments the lack of data around the drug (eg, the "hypothesized mechanism"). It also suggests that the companies intend to work with the FDA more on this.
Was the vote against approval a move to "completely prevent a drug from entering the market and being used", or was it a desire to better understand it before saying "okay"?
Why do you present this as an either/or?
> Clicking "FDA" in the bit you quoted above takes you to a different page
Indeed, where I found that...
> That said, the article may not be fairly representing what happened in the first place, so...
...this is exactly what happened, i.e. I was successfully misled even before reaching your false dichotomy. Yay.
>... your false dichotomy.
I appreciate you giving me the opportunity to answer your first question before coming to the conclusion that I was using a false dichotomy.
I didn't intend to present it as an "either/or", though I can see how it can be read that way. I simply read you saying that they "completely prevent[ed]" something from coming to market when, perhaps, they're not "completely" doing anything and are open to doing it provided that they know more about it. That the "incomplete justification" you lamented may also have been how the FDA felt about the data provided to them.
It could also be for other reasons, absolutely! This is just one possibility that seems very obvious to me. There's no either/or from my end.
If I didn't already conclude that you presented a false dichotomy, why would I have inquired about why you did so? It's also not set in stone; from your reply I can just change my mind afterwards. But why do it in two rounds when I can do it in one?
I understand if I came across as hostile though, I admit it was sadly reflexive, and I apologize.
> perhaps, they're not "completely" doing anything and are open to doing it provided that they know more about it.
That's not a nuance I intended to disregard. Yes, I understand they can revisit the drug's approval later, didn't mean to suggest otherwise.
Gosh I hate natural language sometimes.
Especially when it's sometimes hard to read tone, even moreso from a stranger whose communication style we're unfamiliar with. Even harder still, comments online generally don't lend themselves well to nuance and assumptions can easily be made, such as my leaning too heavily on your use of the word "completely"! Should we hug it out?
Hope you enjoy the rest of your day. :)
The more I learn about pharmacology, the more I realize this is the norm, rather than the exception.
https://www.sciencedirect.com/science/article/abs/pii/S03785...
And that's not even taking into account its cardioprotective effects.
But hey, it can be hard on the stomach in SOME people so we developed alternatives with all sorts of nasty side effects, up to and including heart attacks and strokes (rofecoxib, valdecoxib, etc.) Hell, a decade ago, the FDA issued an advisory across the board that "Non-aspirin NSAIDS increase the risk of heart attacks and strokes":
https://www.fda.gov/drugs/drug-safety-and-availability/fda-d...
Some day we will look back on the attempted replacement of aspirin with these other drugs the same way we now look back on the replacement of butter with margarine (and the replacement of saturated fats with trans fats more broadly).
The agency bears zero responsibility for the pain and suffering its caused by overcaution.
Thalidomide.
Patients (and often doctors) really don't have the skills or information to make an informed decision.
They can however have 'feelings'. This is not the same thing.
To continue my example of thalidomide, the FDA's Dr. Frances Oldham Kelsey prevented millions of American babies from being born with devastating deformities.
At the same time millions of American mothers and their GP's were clamoring for the anti-nausea drug that the British mother's were enjoying. And they too said the FDA was getting in their way.
Experts aren't "made of finer clay" : they just know a lot more than the populace about specific topics. There are other topics where I am the finer clay. See 'specialisation'.