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I've had all three (and more) as have my close pain friends. I can tell you that while actuary tables hold true, we are each individual chemical factories and metabelise medications uniquely. I tolerate Norco well, but not Percocet. My best freind (multiple fusions, bilateral nerve damage, arthritis etc.) is polar opposite.
I find the best advice I get is direct from my doctor and then the pharmacist.
I will tell you that these medications while sometimes necessary can be dangerous. Fentynal almost killed me.
If your situation requires such strong pharmuecuticals I recommend time with a pain managment psycologist. It was he best thing I did. Pain is so intertwined with our brain that we need to look at the mental and nuerolgical conditions along with the physical ailments in order to heal the whole body.
Best of luck and keep us posted.
Tim
Finally, you can use opiates for a lifetime without damaging your body in any way. They are a natural substance, binding with opiate receptors in the brain. Used as directed, there is nothing to fear and much to be gained. Best of luck.
csw2@bex.net
I really wish I knew where to go or what to do...I am out of my mind with pain. I exercise as much as I can, walk, try to use the pool as much as possible, stretches...I just don't think it is fair to be in sooo much pain and no one will help me.
Anyway, back to you...How long have you had your disc problems and is this the first Dr you have seen or did you have to go to lots before you finally found one who would help you? I hope this medicine helps you and please continue to write so I can follow your progress...Thanks and take care
So an update on the medication...I took the oxycontin as perscribed for a week, and I couldn't take it anymore. The IR oxycodone I was already taking doesn't have the sedating side effects that the extended release oxycontin has, so I called the doctor and i'm stoping the oxycontin, and increasing to 4 a day of the 10mg oxycodone.. I literally felt sick and useless when I took the oxycontin...but in doing some research, the drug company that makes oxycontin has changed its formula from OC Oxycontin to OP oxycontin, which is supposed to deter drug addicts. I dont feel like I got to truely try the medication since it's been wayy altered from its older version supposedly.
Sorry for the ramble. But the thing I'm most upset about is the amount of pain I'm still in. I'm waiting til the next appointment and I suppose we'll try something different.
And as far as doctors...I've had intense back pain since 2008, and all of the doctors i've seen since then, have all been kind of arrogant and not very helpful. I'm in my twenties which doesn't help my case...but as soon as my primary doctor decided to refer me to a pain management doctor, that's when everything turned around for me. I've been treated like a human...I finally feel like I'm with "my" doctor now.
I have a close friend in Florida and asked her yesterday what the deal was. She said she didn't know because her PCP prescribed her opiates and her husband's arthritis doctor prescribed his. Both are for long standing chronic pain problems. Neither she nor her husband are terminal or anything like that.
Each doctor may decide for himself that he will not prescribe opiates, but it apparently has nothing to do with the legalities.
Take care, Annette
Take care, Annette
My own personal experience: I was initially started on extended release morphine. I was up to 60 mg per day before I was swiched to Opana ER. In my personal experience, the morphine didn't work very well at all to control my pain. It could be because the dose was too low or that I don't metabolize morphine well. I was taking 30-35 mg of percocet on top of the morphine to get meaningful relief.
When I was switched to Opana ER, it worked fabulously on my pain for the first 2 months and then began to fizzle out. It didn't last the full 12 hours just like the Morphine ER. After I heard about the reformulation of Opana ER and how many were getting sick by the new medicine and that it was 1/2 as effective as the original formula, I jumped ship before I was even put in a position to have to try the new formula. Plus, the Opana ER costs me $255 a month and my insurance paid 50%... when it stopped working the full 12 hours and my breakthrough pain increased, I decided it was not worth the money. The generic equivalent was worse in terms of pain relief.
I have never tried the oxycontin but my doctor almost RX'd it to me. I was hesistant to try it as it now has a known carcinogen in it called BHT. Purdue says it is in trace amounts but I don't feel comfortable taking trace amounts of a cancer causing agent over the long term just how I prefer to take oxycodone IR versus Percocet, which has tylenol in it.
We finally decided on the Fentanyl patches. I love this medication. I am on the 50 mcg/hr patch and I change it every 48 hours vs. 72 hours. The pain relief is very consistent. With the extended release 12 hour pain meds, I couldn't sleep more than 8 hours as if I slept for 9-10 hours, I would wake up in withdrawal and pain so I would have wait for the next dose to start working before I could do anything. With the Fentanyl, I don't have this problem and I like being able to less pills per day.
On ER pills there were also restrictions on when I could take my other medications as if taken too close to when I would take the Opana ER, it would interact with the Opana and I would get severe dizziness and vomiting. I ended up having to set my alarm to take some of my meds in the middle of the night so that they wouldn't interact with the Opana. The main med that didn't like to be mixed with the Opana was the Gabapentin. On the Fentanyl patch, I don't have this problem and I fall asleep pretty much instanly. The Opana caused insomnia for me.
So that's my personal opinion on the different meds. My pain levels are extremely low during the day on the fentanyl patches and I have less breakthrough pain. The pain is typically severe right when I wake up in the morning due to the nerve pain shooting down my legs which opioids don't do a great job on anyway. And, once I get moving and take some Aleve, the leg pain reduces quite a bit. Then I take the Gabapentin around noon which really helps reduce the radiculopathy.
Good luck on making your decision. My doctor has let me try most meds (that I can afford on a continual basis) to see which med worked the best. I think this is the best approach. As Charles said, you may have to try many different medications to find the one that works best for you. Doctors that only let you try one or two meds and then box you in whether your pain is controlled or not, are not taking the right approach. Some of it is due to DEA paranoia I think.

Peace
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