That's of course when the addiction rate for opioids went through the roof. Entirely disconnected I'm sure.
I don't know if they should be used for pain. I'm not educated enough on it to make a statement like that, for or against. What I can say with absolute certainty is Purdue Pharama created a disaster on the scale of natural events by selling legal medication. Every facet of that should be analyzed so we can make sure it never happens again.
That would be heroin. Our institutional memory is woefully short.
My understanding is that they said opioid addiction (in general) was a relatively minor problem and it shouldn’t stop doctors from prescribing them.
“Delayed absorption as provided by OxyContin tablets, is believed to reduce the abuse liability of a drug.”
That's what the FDA allowed them to publish. Possibly the most dangerous single sentence in the history of medicines.
It is actually true though. Delayed release would be expected to reduce abuse liability.
That doesn’t mean OxyContin is not addictive, it just means it’s expected to be less addictive than immediate release oxycodone.
Although manufacturers have created a tamper proof version, but that just led users to move to heroin.
The first fault is that even the studies done by Purdue prior to release did not indicate anything close to the 1% addiction rate they advertised, it was more like 8-12%.
The second, most Oxycontin users who aren't well off eventually move to heroin, because the effects are very similar, and the street price for Oxycontin is much higher. Ironically, where Marijuana was demonized for a nonexistent gateway property in the original war on drugs, Oxycontin was actually demonstrably a gateway drug for heroin.
There's a very well researched episode of the podcast "Behind the Bastards" hosted by Robert Evans that drills down exactly into all of Purdue's dirty little secrets surrounding Oxycontin. Once you realized just how many numbers were fudged, how many studies fiddled with, it becomes clear just how much had to be made to go wrong in order for this epidemic to really kick off. It's quite damning.
The source of the issue really is just how hard Purdue was fudging their data. And I mean, you can say that a drug company shouldn't be the sole tester of it's own drugs and I'd agree with you, but good luck getting average people to want to pay for it by funding the FDA.
Which yes, is a pretty logical follow through, but also you'd expect more rigorous proof than "we think it'll do that" for medicines.
https://www.aafp.org/afp/2018/0301/p348.html
is one example, for patients presenting in the ER with extremity pain, and one that's specific to impacted wisdom tooth extraction is:
https://www.ncbi.nlm.nih.gov/pubmed/28586638
("CONCLUSION: Codeine 60 mg added to a regimen of paracetamol 1,000 mg and ibuprofen 400 mg does not improve analgesia after third molar surgery.")
There's a study I'm very curious to see the results of for this question for post-caesarian patients: https://clinicaltrials.gov/ct2/show/NCT03372382 (study is still underway).
And there's been really promising results for other forms of post-surgical pain management. One great example is the use of a QL nerve block administered during surgery to manage post-caesarian pain:
https://sci-hub.tw/https://rapm.bmj.com/content/early/2019/1...
"QL block has been associated with reduced postoperative opioid consumption and pain scores in patients undergoing cesarean delivery, [... but more study is needed because the studies weren't big/comprehensive enough ...]"
There are lots of caveats here (in other words, don't believe some random schmuck on the Internet over your doctor) -- different types of pain may respond differently, different people may respond differently, etc., etc. Ibuprofen impairs clotting and is inappropriate for use with some patients and some types of injury. Acetaminophen has to be dosed carefully to avoid liver toxicity. No free lunch. But it's certainly promising from the perspective of non-narcotic pain treatment _in some circumstances_.
(Please don't misconstrue what I'm saying, of course, as suggesting we can or should eliminate opiates. There's a place for everything in our arsenal. But there's been a lot of progress in the last decade that open up alternatives in some cases.)
Glossary, in case it's helpful: acetaminophen (US) = paracetamol (UK) = tylenol (brand name). ibuprofen = motrin = advil. oxycodone/acetaminophen = percoset (brand name; ratios may vary).
I'm certainly not well educated in medicine, so it's hard to say whether my experiences can be generalized to the broader population, but if my experiences are at all common it does make me wonder why the are so broadly prescribed, and why I was never advised to even try NSAIDs before escalating to opioids with their associated side effects and addiction risk.
I had a bone marrow biopsy, where they can’t anesthetize you and sure burrowing into my bone with a scalpel hurt. But whatever. Life is pain.