Pain Management :: Withdrawal From Gabapentin
Dec 30, 2013
So I had back surgery in July. I had used gabapentin the 3 years prior. Max dose 1200 mgs. My PM doc told me to take 3 months to get off of it. Seizure risk and all. I am now down to 400mgs a day. I have tried a few methods....right now pushing each dose out more time. So basically in withdrawal all the time. Hopefully someone can tell me a better way.
Years ago when I quit using Xanax to sleep I would make a cut, then hold. Wasn't painless but this is hideous.
Mentally I am strong no addiction issues. Just rather not be sick all the time.
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After 3 years of taking this medication I am ready to come off. My doctor told me not to stop cold turkey due to seizure risk. And sounds like he think I could do it in a week's time.
Hoping someone here has had some experience with coming off of this medication. It truly helped before my surgery this summer.
I don't love the side effects.
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I wrote in march about my anal fissures driving me to despair. Meanwhile I had 5 surgeries including 2 botox injections into anal sphincter without success, one double sphincterotomy that should have fixed the problem but wound infection occurred. One surgery with laying open of perianal fistula and the last one was a drainage of a perianal abscess. The last two led to hospital stays of several days. I have been prescribed oxycodone 10 mg since mid feb but usually only took two doses in 24 hours, on bad days 3. Approximately last three weeks I have been on targin 10 /5 mg twice a day . As my pain drastically improved after last surgery a week ago I stopped slow and fast release oxycodone 3 days ago.
Since last night I am suffering terrible withdrawal symptoms that leave me restless, agitated and unable to sleep. How nan I deal with it?"tried valium yesterday, temaze tonight but it doesn't stop. Can't stop moving and twitching but I am dead tired...
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Any experience with gabapentin causing chronic pain problems when taking or withdrawing? During my taper I developed major issues with sciatica and my hip. I'm also taking forever to heal from a frozen shoulder injury (14 months). I had preexisting issues. My guess is it's from all the couch time necessary to heal. But it feels like it shouldn't be this bad. I'm only 29
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Was on Gabapentin for a year and worked up to 3200 mgs a day. Was taking it for Osteo Arthritis in feet and knees. Didn't do much for pain so decided to get off of it. My Dr said to take 1600 mgs for 5 days the drop to 800 mgs for 5 days! This was 3 weeks ago still fighting withdrawal. It's eased up some but still have some anxiety and like pressure in my chest. Almost makes me feel short winded at times. Has anyone else had this and how long will the withdrawal last? Have heard the longer you was on it the longer it takes. Tired of it just want to feel normal again.
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Was on 600mg Gabapentin 3 times a day for peripheral neuropathy to little effect. Was prescribed Amitriptyline, took 25mg for 3 days then 50mg for 5 days - replacing the 2 Gabapentin at night. Reduced Amitriptyline to 25mg after awful side effects. Took for 2 days with 300mg at night (in addition to the 600mg in morning and new GP said stop Amitriptyline and increase morning dose to 900 mg. Was OK for a while, but then feet and lower legs started severe pins and needles, difficult to walk. Disturbed sleep last night and feet and legs still bad. Is this withdrawal from Amitriptyline? How long will it last? GP rang and said gradually increase Gabapentin to 900 mg 3 times a day and if necessary go to 1200 mg 3 times a day. Any suggestions? Will this gradually get better?
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Does this help? If so what is your dosage?
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I have now fully weaned off of Gabapentin. After several months of constant right arm pain - mostly in my deltoid - I now only have intermittent pain episodes. However, my hand and neck sensations of being swollen have returned to about 50% of their worst. My right hand dexterity has definitely declined again.
I also have to note that I've been on vacation from my desk job for a week - so maybe it was all the computer work putting the strain on my arm? I have had to learn to mouse with my left hand, so at least I minimized that strain from my right.
Anyone else go off Gabapentin and have unexpected results? How long until it is fully out of your system?
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My family member said she has a drug called gabapentin and said maybe it would help me thru the tough part of my wd. As its a med for nerve pain. The worst is the crawly skin for me..anyone had any experience. I don't want to take something that is going to minimize the pain then once I stop taking that it come on stronger than before. As I've heard with people taking tramadol for wd.
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My doctor just put me on this today, to help me sleep...I haven't taken it yet, as I get scared with taking new meds. Should I take this medicine? Is there major withdrawals, if I forget? And does it actually work? What symptoms r most common? Sorry for so many questions...I'm just a worry wart. I already went through withdrawal symptoms a few months back, b/c I quit Effexor slowly, and switch chef over to Wellbutrin. I had shocks, shakiness, panic, etc...it was scary...and I don't want to start a new med that's going to do the same thing...so can someone please help me? Thanks.
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I was switched from Nucynta 50mg to to Opana 5mg (OxyMorphone) by my Pain Mgt doctor and I have a total different experience. I don't know if they messed up or what, but here's the issue.
While I was on Nucynta, I would take it, and eventually feel the effects, i.e. the lightheadedness, the "high" feeling, and also the pain relief. The reason I was switched was that Nucynta gave me migraines. Bad enough where I got ill and had to run to bed with all lights off.
Onced I was switched to Opana 5mg, things were different. I took 3 last night, my very first dosage, and took the first. No effects, no pain relief, no "high" feeling, nothing. So, about a hour and fifteen minutes later, I took another one. Still nothing. So I wait again, same amount of time, took a third pill...... Nothing.
So, when I saw the doctor originally and was switched, I was told that Opana was an equivalent to the nucynta. So, if it's an equivalent, why did I go from 50mg to 5mg? I'm just curious. I know they are different drugs and probably manufacturers. Can anyone shed some light on this bizarre issue?
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I was in a car accident about a week ago and 4 days after the accident I started having pain on the left side of my ribs right under my breast when I take deep breathes, yawn, sneeze, ect. It a little swollen but doesn't hurt to touch. what could this be?
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Couple days ago I stepped out of bed and almost hit the floor as the excruciating pain shot through my calves. I have not exercised or done anything extreme. I have tried stretching and over-the-counter pain meds ..
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I have excruciating pain on my right side almost constantly and when I take a 1mg xanax, my pain goes away. Why is this? A Lot of people question this when I tell it but in all honesty it works. I wouldn't be telling it on here as telling it on here doesn't benefit me at all. I would just like to know why a xanax will stop my pain on my right side. Any ideas?
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I have asked to be removed from all pain medications as they were not helping at all and did not want to just keep increasing dosage. So my PM Dr. suggested i try Ativan or Diazepam before bed and also a muscle relaxant called Baclofen for spasms during the day (which i had been on in 2013) it did not work, but he insists on trying it over the Soma 350mg i had been on before the surgery.... any input
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I have been on 3 pills a day of norco 10/325, I want to slowly taper off. I need a plan that would be with no W/D's. I thought about starting a reduction of 1/2 a pill every week until I am free of the pills.
I also need to stop taking celexa, I am going to cut back 1/4 a week to iam off.
Will this work?
Or do I need to get suboxone and is that addicting.
Once off the pills, I don't know what I will do about my chronic pain.
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My dr. did a CT scan on my left side to see if I had sciatica as I had a lot of symptoms of it. It showed minimum damage to the nerve. I was not told what to do next? Should I get a follow up with what kind of specialist? Would a MRI show more information then the CT scan?
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will i have withdraws after taking suboxone 3 weeks? they put me back on pain meds because i having surgery soon
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I went to my Pm yesterday and let him know that I wanted off the methadone. So since I had to see the NP because it was considered an emergency visit they decided they were going to put me on the patch where you wear it for three day then take it off. So I asked about the side effect and after hearing them something in me panic and snapped and I said forget I want off of everything. So as off right now I am coming off of the methadone. I decided that with the scare of my heart and the new neurological problems they only way to know is if I come off of the meds. I am still on the Topamax he did not want to take me off of that because I have been on it for over a year and never had a problem. SO I am hoping in with 2 months we will know if it was the meds causing the neurological problems or the something else.
What made me snap was I was telling him that I wanted something for the muscle because I was having a lot of spasms and tightness and off of the methadone and he totally ignored me and said well we are going to give you something a lot strong and this should work since the methadone has not been working. It was as if he was not listening to me. He said to me you are going to Cleveland clinic (CCF) to be treated for the muscle so the will figure it out soon, I said yes but I do not get medicine from them because I have a contract with you. I don't know why he would not give me a muscle relaxer but I feel better knowing that I am coming off of the medicine for a while I just hope I can handle the pain long enough to see of it is neurological or a side effect from the methadone....
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.I had a C5-C7 disc fusion done 5 years ago that alleviated all of the pain in my neck and shoulders. What I am left with is a severe case of peripheral neuropathy. My feet and legs are numb to the touch but hypersensitive when I walk so I cannot go very long distances without the tingling burning throbbing pain. This pain is heightened at night when I go to sleep thanks mostly to the 300mg of Lyrica twice daily. I had an EMG nerve conductivity test performed which of course indicated severe neuropathy.
Now I am going to a neurologist who says I have to put up with the pain. I am going back on Monday to my neurosurgeon to ask for a lower MRI (never done) and I wanted a referral to PM because the pain is out of hand on 600mg of Lyrica daily. I have been on Oxycodone before and hated it and I do not like the stigma attached to these drugs so I thought I would ask my doctors to consider Methadone. What does everyone think? I know Methadone has its own stigma but is long acting and something I NEED right now and probably for good as I have had this neuropathy for 5 years.
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I have suspected Piriformis Syndrome & SI Joint Dysfunction also causing sciatica, have also had some nerve pain in the back of my thigh, occasional calf cramps, foot cramps, and foot pain. Since my last Cortisol injection into my SI joint it has made everything horribly worse, I cannot sit now for very long without severe left foot pain that makes me feel nauseous it's so horrible. I have informed the consultant of this and am on a waiting list to go back and see him, this is the 2nd time the injections have caused me extra pain so have now lost faith in these and want to try alternatives.
My consultant previously wanted to put me on Amitriptyline but I have been on this before and was taken off it due to serious sedative side effects (even fell asleep eating in a restaurant) was on a small dose and still didn't improve with time. So I've read that Nortriptyline is an alternative with less side effects, can anyone advise if they have had less sedative side effects with this than Amitriptyline please?
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