Chronic Pain Support Group
Physicians and professionalsdefine pain as chronic if it lasts longer than three to six months and is persistent. It's distinct from acute pain that is a direct result of injury or trauma. This support group is dedicated to those suffering from chronic pain. Discuss treatments that have worked for you, find advice for your specific experience, and find support. You're not...
honor435, please let us know if the MScontin works for you, because if that's the case about the oxycontin not coming out with a generic version until 2013, then I need to go to plan B
Stay Gold!
Oxycodone SR is the generic name for OxyContin. At least that's what it used to say on my prescription bottle. I got it in 20mg and 40mg. My husband also once had a bottle of generic 80mgs. I also took Oxy IR (instant release) for breakthrough pain, which I believe comes in a 15mg formulation, which may be what you're thinking of... I know the IR (also known as Roxicodone) comes in 5mg, 15 mg, and 30mg. I think it is also made in generic form as 10mg and 20mg instant release. However, I believe that Perdue Pharma now also makes a 15mg OxyContin, but I don't remember there being a 15mg when I was taking it...
And no, none of those have tylenol in them (not oxycontin or its generic, oxycodone SR or oxy IR), they're all just oxycodone and fillers.
So yeah, i'm still confused about all of this. I KNOW I took a generic.
I do not have the info handy but if you look into it online I bet you can find it!
Just wanted to let you know!
I hope ms contin helps me too, so sck roller coaster ride.
I'm sorry it didn't go as well as you had hoped. I understand that you had side effects, but I am curious to know how well the MSContin did its intended job- relieved your pain. Did it help with your pain but make you tired? Or did it just make you feel terrible and give you no relief? If it helped with your pain, I would say that you need to give it more time. All meds have side effects... I spent a few weeks recently with some pretty icky side effects from a new med I was taking for acid reflux- but it completely stopped the burning pain in my stomach and chest, so I stuck with it... and my body has gotten used to it. So, if something like that can cause problems, of course a strong narcotic like morphine is going to have side effects... so my advice would be to stick it out for a while to see if the side effects diminish as your body gets used to the stronger narcotic. I think it's hard to expect no side effects like what you described from a narcotic. I've been taking the same dose of methadone for SEVEN YEARS with no change (which means my body is totally used to it- to the point that it gives me NO pain relief), but it still makes me tired even after all this time! However, nowhere NEAR as tired as OxyContin did- I literally slept away a year and a half of my life when I was on that. So I couldn't live with that, so I chose something that gave me less severe side effects... so now I just take a short nap in the afternoon, when I get the most tired. It's not ideal, but I've had to make more than a few adjustments to my life because of my pain (that's an understatement). So that's my advice- I would give it at LEAST a week for your body to adjust- you're throwing some pretty strong medication at it.
However, I also understand that some side effects can be deal-breakers with certain meds. So if you really feel that you can't work with the current side effects, maybe you should contact your doctor and see if he can start you on a lower dose of MSContin... I forget, did you tell us what dosage you are taking now? You could also try to shift the times you take your meds to try to work around your work schedule- to make it so that the time you're least tired (like for me, I feel the least tired for the first four hours after taking my meds) is the time when you're working.
It sucks, I know.... there is just no damn miracle cure for pain- and then the things that HELP just come with their own problems (like not being able to go to the bathroom for three or four days at a time- fun!) so it's like a choice between the lesser of two evils sometimes- the meds that help your pain (complete with side effects) or just trying to go it alone with your pain (and massive amounts of Advil, for me!). It's so damn frustrating because there's no easy answer. I know some people who had to stop working and go on disability/SSI because of that very thing- they had too much pain to work, but the meds that RELIEVED their pain made it impossible to work. So either choice (taking the meds or taking the pain) was going to change their lives drastically. It makes me very angry when I think about it, about the things we go through dealing with chronic pain, losing our entire lives sometimes. Pain is such a basic thing, something every human body experiences from time to time and always has- it's not some new 21st century discovery. You'd think that in the thousands and thousands of years, SOMEONE would have discovered a way to STOP pain without having to cloud our minds with drugs. Opiates don't actually do anything for the source of the pain- they just change your PERCEPTION of the pain. Where's the meds that actually stop the pain itself? It's crazy that there isn't anything yet.
Anyway, back to your problem. I also think you definitely need to call your doctor and tell him or her your concerns and see what he/she recommends. Your doc might have a plan b in mind (or i guess I should say a plan c, since this was plan b) that will work better. Our bodies are all different... morphine may not be right for yours. Or it may be if you give it more time. There's no way to know. One thing I can suggest though, when it comes to a long-acting pain med, is to maybe discuss the fentanyl patch with your doc. Have your ever used them before? I have seen ssooooooo many people say they get great relief from those patches with pretty minimal side effects. I used them for a little while and had no side effects. Another suggestion I can make from my own experience with pain meds is Dilaudid. I don't know if you are deteremined to stay with a long-acting pain med, but if you decide to go back to a short-acting, maybe try Dilaudid if you have a problem with drowsiness. Dilaudid tends to cause less side effects than most opiates, especially when it comes to sleepiness. In my experience, it was amazing for pain relief and lacked most of the side effects of other meds. There was a long-acting version of Dilaudid (hydromorphone) out there for a bit, I think it was called Palladone, but it seems to have disappeared and i don't know if it has been replaced yet with a newer long-acting one. Anyway, there are a lot of other options if the morphine doesn't work out- but I think you need to give it more time than just a weekend. And you definitely need to call your doc to at least share your concerns about the side effects and try to follow his/her recommendations. Let us know what the doc says!
Best of luck with all of this... you WILL find the right med or combination of meds for YOUR body. It just can be a long, frustrating process sometimes. Hang in there. :)
the reason many won't pay for it right off the bat is BECAUSE it is expensive...they want to make sure you have exhausted all other (read: cheaper) options before they will cover. it sounds like you have. mine had a list of drugs that i HAD to try before they would pay; i had tried almost all of them. one of them was, however, the patch. my doc doesnt like prescribing it at all; but b/c my ins required i try it, he had to write me an rx for it just so we could say that it didn't work. go figure. anyway, the total cost of my rx w/o insurance is about $1,500 a month. no way i'd be able to afford that!!!! good luck.
Ive had 2 migraines since starting and stopping the ms, im back to short acting- for now.
Oh, my ins said they would cover 40mg oxycontin, not the 20mg that I need!
I looked for med cost help online- nothing.
Thanks everyone I will keep you posted.
i can try and help you if you want to PM me. I also was on the ms contin for awhile and it made me really out of it. my current rx really helps control my pain and I am able to work; and NOBODY knows i am on it (unless they are one of the 3 people I trust, doctor included). i just feel for anyone that isn't able to get the meds they know work for them b/c of insurance issues.
good luck!!