I do share other people's skepticism of the medical industry as you might be able to tell. He should have done more research, agreed.
They'll stay up to date with what is standards of care, but even that is dictated to them by their EHR software or what they expect your insurance will cover.
When I've gotten prescribed a new medicine, I don't really recall a doctor ever even telling me what side effects to watch out for. At most, they've told me not to drink alcohol while on someone.
I’m convinced anyone who doesn’t do this is either too young to know better or too dumb to have been paying attention.
I thought I was world worn and tough.
Then came AI and I was again on the doom and gloom train. Then I had a moment, realized this just the new thing and dropped it down a few degrees.
What’s next?
You kind of have to be a monster to say something that callous.
https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/02...
Among other things, it says “Physical dependence and tolerance are not unusual during chronic opioid therapy.” I'm no expert, but I think that explains why warnings about dependence weren't more pronounced. The drug was supposed to be distributed in a tightly controlled fashion due to these risks, after all.
In retrospect, the warnings at the start, and the information for patients read like recipes for abuse, though.
For dealers, it gets people through the gateway. For the anti drugs crowd, it's the equivalent of preventing teenage sex by not telling them how it's done
“Also at the time of OxyContin’s approval, FDA product labeling warned of the danger of abuse of the drug and that crushing a controlled-release tablet followed by intravenous injection could result in a lethal overdose. There was no evidence to suggest at the time that crushing the controlled-release capsule followed by oral ingestion or snorting would become widespread and lead to a high level of abuse.”
https://www.fda.gov/drugs/information-drug-class/timeline-se...