Hacker Newsnew | past | comments | ask | show | jobs | submitlogin

We spent the better part of decade catching and locking up doctors who prescribed opioids out of guidelines, so much so that doctors are now terrified of prescribing them to people who legitimately need them.

The problem is that the prescribing guidelines, which were written by the pharmaceutical companies themselves, described a regimen that would get pretty much anyone physically addicted to their product.

So you had doctors acting in good faith, prescribing medications only when indicated and following their manufacturer's prescribing guidelines, inadvertently creating new addicts where the manufacturer's literature said there would be none.

Not only that, but we spent several decades treating chronic pain patients with opioids, such that they are completely dependent on that class of drugs to manage their condition. Only very recently have prescribing guidelines adjusted to reflect the reality that opioids are not a good treatment for chronic pain. When those pain patients are driven off of their opioid prescriptions, even if their doctor is well-meaning, some of them turn to heroin/fentanyl to manage their pain.



Shouldn't the FDA be checking whether the guidelines written by the pharmaceutical companies are safe?


The guidelines are almost always on the conservative side of safe because people who died as a result of taking the medication the manufacturer recommended way turn into slam dunk lawsuits. Part of the reason the opioid problem flew under the radar is because people got hooked and weren't dying until they OD'd so it never came back to bite the manufacturer. What are the odds of another opioid type situation? What else could the FDA do with those resources?




Guidelines | FAQ | Lists | API | Security | Legal | Apply to YC | Contact

Search: