I have been on a patch for about four years now and use cocodamol for break through pain. At first I started on 10 micrograms but found that to much and so reduced it to 5 micrograms. However due to other problems my GP on advice from the pain management people want to increase it back up to 10. My main problem with the patch is that once it's on its on and there is no way to reduce dose. I am quite happy to stay on 5 and wean myself on and off cocodamol as required.
To be honest I actually question myself if it's a placebo because I personally don't think it works that well, maybe takes the edge off. Previously I was taking a lot of oxycodone so the pain clinic wanted to get me off them after just over a year
Hello Fibroguy66, hope you are managing well. I've been using buprenorphine 5mg for the past 5 years. I felt horrible for the first two weeks. Up till now I have skin reaction to it. I can put the patch only on my arms as on my chest and back skin gets infected and need antibiotics. Because of that i can only use one brand. For me it was prescribe for arthritis in my hips, which ofcourse fybro makes the pain feel worse. I'm also on pregabalin which is for fybro and my other health condition.
I don't want to increase the buprenorphine because if I do it now what is going to be in 10 - 20 years time ? My arthritis will not get better and the surgeon doesn't want to operate my hip - too risky.
So yeah speak to the GP if it's OK to increase it but remember, this is not a tablet which you can easily decrease. Think about withdrawal from it ,what if the the higher dose doesn't work either . GP will advise you or the pain clinic.
Doctors always say it might take time to build up in your system. I never really believed that, unless it's something your titrating up. I always think the amount of pills we take probably does more harm than good. I take pills for everything though. I haven't heard of that drug, but if it isn't working I would definitely find out if there is another. It's all hit or miss. It's really hard, especially if the doc doesn't get it. I'm fairly certain my roommate has it. He is also diabetic. He was asking for something for pain and the doc told him he needed to deal with the reality. What a bunch of BS.
Hi fybro guy hope your having a reasonable day, I have tried lot of meds, including butec patches I had 10years on 5/10 microgram came off them as I suspected the cause of nightmares, after weaning off them proved right. A few months ago pain consultant advised I try them again, I did for about 3months but felt they did not help, I continue to take nortriptyline 10mg one at night which I up to 20mg if had a couple of poor quality sleep, Dr advised I can take upto 70mg (I don't think I would consider this) for me Prescription drugs are not helpful, when I had a few different med I found it difficult to assess what was helping and what was making symptoms worse, I do feel you have to try different options and observe the effect, but I concluded after a few years of trying different meds not for me, I now only take the Nortriptyline and paracetamol when I really have to, going down the holistic route, I occasionally use a TENS have consulted osteopath, physio (privately) which I feel helps,CBD helps with mood, also mindfully of pacing myself( Which can be challenging) It is all trial and error I know but I do feel my pain levels now more manageable, wishing you good luck with your journey π¦π
nortriptyline give me bad dreams & somewhat nightmares etc,so much so you remember them the next morning & there so vivid you could write a good book out of it all.Not for me thankyou π
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