Honestly don't know the answer. Maybe no one here gets those.
(begin off topic rant...)
Consider yourself lucky, my new ins wont cover any more than 60 opana er per month. It is not enough, not even close.
Get 30's right now and would be nice to switch to 120x15mg generics but they wont cover it. Not sure what to do. Certainly not gonna panic over it but do want to continue using this med for daily necessary pain relief.
Being in bed a good part of the day really sucks when functionality is easily achieved with the right meds administered the right way. Do doctors and ins companies not get this? Maybe things are so far gone and messed up that they trust no one and really don't want to help, its all about making and saving money.
People who just want to function and have legit issues where the meds help so much get treated like absolute shit, even falsely accused of drug
seeking and abandoned by those who are most able to help. Its so wrong. Wish there was some punishment we could hand out.
Its crazy, if everything were legal and over the counter I would just pick what it would take to achieve functionality every day, fast and first thing in the morning bam get right, get out of pain, and get on with a productive day.
The way it is now just sucks, undermedicated struggling, lingering debilitating pain, non productive, in bed often and losing the progress made on physical condition that was worked so hard on. Must fight on but things could be so much easier and better if the doctors and ins companies would just help out and cover a bit more.