Today my dr gave me gabapentin. She's thinking it will help the pain. I'm wondering if anyone knows anything about this medication? Does it actually work for pain? I just want relief for the daily pains. Any suggestions would be great!
Hello, I take gabapentin 3 times daily. Honestly I am not sure how much it helps me. At first I started out at 1 tab in AM and PM. Now I am up to 1 in AM 1 at noon and 2 at night. If I miss a dose at night I can really feel it. I do not sleep well, and I get nerve pain/jitters (I get the restless leg syndrome but it is in my buttocks too and I am up off and on all night) Anyhow, I do think it defintely helps me with sleeping...huge difference. Beware, I had a lot of side effects in the beginning, give it a good couple of weeks and they subside. Ecspecially the foggy head/tiredness. Sorry I can't be more help. I say give it a try, hopefully it helps!!
Gabapentin is mainly prescribed for nerve pain. Fibromyalgia is known to cause nerve pain. I'm taking it just now for post Shingles nerve pain. I am taking a very low dose, so I'm not concerned for myself. But, the high doses are the ones to worry about. Tapering both up and down is necessary with the higher doses. My PCP told me that is in the range above 3,000 mg.
Even at the very low doses, Gabapentin (Neurontin is the brand name) can cause drowsiness, which I'm noticing as a side effect. This is listed as a known common side effect. Of course, I am also a light weight when it comes to pharmaceuticals and have the added bonus of Multiple Chemical Sensitivity (MCS), so less is more with me and pharmaceuticals. Still, just the same, drowsiness is a common known side effect that you need to be aware of.
My doctor put me on gabapentin last May, after I had been suffering severe fibro pain for nearly a year under another doctor, and within 2 weeks, I was feeling like a new person! This medicine saved my life, as far as I'm concerned, because I was effectively disabled by the fibro. I tolerated the medicine well, if there were side effects I hardly noticed. It has also seemed like the longer I've taken it, I continue to slowly get better. I do see now that I was suffering with multiple types of pain, because I still suffer pain, but it's a much more "normal" type pain - for lack of a better way of saying it, ha! I can sleep now, I think more clearly, I can do things! I don't think I'll ever be the person I was before the fibro came into my life, but I'm so much better after the gabapentin. It is my one medicine I really trust!
I started taking it yesterday. With the first pill I felt like I was a little drunk. That's the only way I could describe it. I also take 3 more meds for my night time pain/restless leg/insomnia. Night time is the best right now. I just don't know much about fibro. I feel kinda lost actually. Thank you so much for replying. :)
I took Lyrica for Fibro nerve pain and found it made me loopy like I was drunk and I could not tolerate it so I stopped. A couple years later my doctor gave me gabapentin for the same thing as I wanted to try it again. It takes a couple weeks to supposedly start working and I took it for 3 months and found it didn't help me whatsoever which was frustrating. For me gabapentin does absolutely nothing.
Neurontin/Gabapentin has been a miracle drug for me. It helped not only the Fibro pain, but my nerve pain I have due to inflammation compressing nerves. I have an inflammatory arthritis disease, Ankylosing Spondylitis. My ulnar nerve, sciatic, & a nerve in my neck & shoulder were bad, very painful. My dr had me work my way up VERY slowly. I basically added 100mg a day until I got to my target dose of 1800mg. If I had side effects, I stayed at the same dose for 3 days to stabilize before adding another 100mg. I think I only had issues twice.
I was put on gabapentin about 2 yrs ago as an off label treatment for anxiety. My neurologist upped the dose when I developed neuropathy, and when I started having chronic migraines, they upped it some more. I just got diagnosed w fibro, after a lot of " process of elimination", very glad it isn't ms. Anyway, I take 4 800 mg pills a day. Honestly, they help the neuropathy pain a lot, but I seem to have a different kind of neuralgia, caused by fibro, that causes severe numbness& parasthesia & the neurontin doesn't help this at all. It also seems to have zero effect on my migraines, and the only reason it seems to help w the anxiety is it makes you feel drunk & disoriented. The only good thing I have to say about neurontin is it Really helps w the ants on your feet feeling of neuropathy.
you really have to watch for side effects i was taking lyrica and it started affecting my vision really bad , and all of those nerve drugs are the sister drug to lyrica so be careful if it makes your vision blurry stop taking it ..good luck
I started Gabapentin. I was prescribed 300mg 3x a day every 8 hours.I didnot take the whole dosage I was afraid I am always concern when I start a new medication.I have chronic pain due to multiple conditions (3herniated dics,IC,IBS, but Fibromialgya is the worst! ) So I started with 200mg 2x a day and on the 2nd day I was able to move without feeling like I have weights on my arms and legsmy muscles dont feel tender to the touch anymore. it gave me energy enough to do daily activities like taking a shower, changing my babys diapers, cooking etc. on my 3 day I was already doing this I could not do before. I have Fibromialgya. I also take norco but even 5 norcos would only ease the pain a little but kept m eunable to perform like I wanted to.Gabapentin gave me my life back! I know it does not work the same for everybody and that we all react differently to different medications.I guess my best advice would be to try it and see if it works for you. Best wishes.
I have been on a low does of Gabapentin for mental illness for years. But when the dosage was increased (majorly) then the pain from my fibro has been lifted. I can handle water hitting me (before this was like needles all over to me). I can move and walk for hours without pain and swelling. This is my lifesaver. Oh and sleep, wonderful welcomed sleep finally. I am not in pain from just laying down as I was before. This is my miracle.
I have Fibro & have been on Savella. Im in the 7th week of severe pain /fibro flare. Today Dr put me on Gabapentin, About an hour after the 1st dose, I felt a little odd, it has helped the pain, but my head feels disconnected to my body, feel lightheaded,a little nausea, spacey feeling,dry mouth. I took one 300 mil pill,and on a plan to work up to 1800 mil a day slowly. Are these side effects normal? Do they go away? Get stronger or stay the same? I feel a little jittery as well. Thank you so much for sharing.
Ive been on gabapentin since I was 16, im 28 now. Back then they didn't have many good mood stabilizers, so they gave it to me for bipolar, I have irritable bowl too so they thought it would help that maybe, but I took it mainly for bipolar. I now have sciatica and they believe I may have Fibro bc of the wide unexplained pain all over. It really is a great drug, yet now I am on a very high dose. I take 3 300mg pills in the am & 3 300mg at night (I can break it up during the day if I want) so 1800mgs all together. I also became addicted to a medication a doc gave me when I was 15 so they gave me that in the hospital and I was knocked out for pretty much 3 days straight. I never noticed any side effects bc I started off with the medicine, unaware of anything. Maybe a little tiredness & dry mouth but nothing major. I do know being on it for over 10 years I wouldn't want to stop taking it bc it does help some w my pain (again ive been on it very long so im sure it will work much better for you) & really helps my nervousness. So if you have any anxiety you will be amazed at how much better it makes you feel on that end. Where I get my meds from have changed what the pill looks like (im not 100% on this but its a side note) & I have noticed a side effect a lot of ppl have, including my mom, that it makes you feel kinda drunk & its very easy for you to fall asleep if you try to even sit to rest after taking it. But other than that give it a go! There usually a lot less side effects w this drug than lyrica & other fibro/pain meds, at least w me, also when you compare the strength you need to get any kind of relief. Hope I helped at least some..i just have a lot of experience with this drug bc out of everything ive been on, this is one they never had to take me off of & in 12 yrs only had to tweak the dose a handful of times. None of the side effects are worrisome either, like lyrica which caused me horrible depression.& to the person above..don't let the jerking go on to long w out telling your doc bc the tremors may not go away if they are severe right now..best wishes!
O was put on lyrica, but insurance wldnt cover it, so I'm on gabapentin. I've been raking it for two days now, and feel a lot better, but my pain remains. If my doc would give me a stronger pain med, I think my pain wld be completelyknocked out. Yet, my Dr pretty much laughed me out of her office, saying I shld get in touch w a shrink. She thought its my amxiety causing my pain. She also told me to quit my job and go on disability! I was so upset, I just balled my eyes out in front of her. I demanded the lyrica, since my pain levels are always at an 8-10. I hate when Drs don't see anything wrong w u physically, so by their terms, u are fine. I'm at my wits end. Any advice??
Oh no that's awful! You sound just like my mom. He made her feel awful & she is applying for disability, but she hasn't been able to work. I'd say twitch docs that's what I told her bc there are some good ones left. Mine is awesome & is trying all he can to get me outta pain, which has involved trying any good med, of course trial an error. Pain meds sometimes are needed at least need to be offered. He pretty much said the same to her, but then put her on a pain management plan, yet made her feel like a drug addict even tho she's been w him 22 yrs. If he doesn't care now, he won't later. Find someone who will fight as hard as you to get all the relief you can to enjoy life!
Gabapentin has saved my life. I've tried almost every psychiatric drug over the past to years. I was extremely Manic which eventually landed me in jail. I would sleep 3 hours a day but get nothing accomplished when I was awake. I couldn't even write this post back then. I started self medicating with Alcohol and Marijuana is dumb my racing thoughts. I recently started Gabapentin and sure enough in 2 weeks, it changed everything. I can think clearly, can focus, sleep and dream (couldn't get into rem sleep for years), more motivation(I'd lay in bed all day before), and an overall well-being feeling rather Anxiety all day and night. I also feel more confident than I've ever felt and I'm just 3 weeks in and feeling better each day. I don't drink hard alcohol anymore and I was up to a 750ml a day for about a year, which also hurt my wallet. I'm on 600mg x 3 times a day. I works so well, it brings to tears of joy when I think about what it has done to life. I hope that it can work for you as well. :) best of luck in finding a cure for your Bipolar Syndrome! Keep the faith.
I have been on Lyrica for a year, and cannot take the side effects anymore, especially the weight gain. Have you had any weight gain with Gabapentin? I have not only gained 60 pounds in a year, but have swelling in legs and feet, plus the severe dizziness. I obviously read what side effects you experienced, but have you had any of the ones I mentioned? Anyone else that reads this, please comment and let me know if you have taken both of these drugs and your experiences, I'm desperate but don't want to be a test rat if that makes sense.
I am so glad you got a new doctor. I had the same issue. I had a good doctor but then he transferred to another area and I was assigned a new doctor. I stuck with her even though I felt like she didn't take me or my pain seriously. He talked to me like I was a child. She also took away any paid meds I had to "change to something better" but I realized later she was only getting me off of all the pain meds. I ended up with nothing but 800 mg ibuprofen and otc drugs. I looked around for a different doctor but they all had a free practice or they didn't for a good reason. Anyway, I just lucked out early in Jan and got a new doctor. He has already helped me. Right away I felt like he BELIEVED ME! He seems to be very knowledgeable about what I'm dealing with. He asked me if I'd ever taken gabapentin and when I said no he asked why. I'd never heard of it and no other doctor had ever told me about it. It started helping me right away and it is amazing. It made me so angry that I'd been suffering in so much pain for so long and this could have changed my life so much. I would have liked to have a good time during the summer instead of laying in bed in pain and wishing I could move without hurting so much.
Anyway, I am also like the person above that is a light weight when it comes to drugs. I was given 100 mg caps so I could start with 1 and increase needed. I took 1 of those for 3 nights in a row and it really helped my pain but I felt so drugged and couldn't get out of bed. I slept almost a full day and then I called the pharmacist to see what I could do. I ended up taking the capsules apart and taking half of the contents every night for a few weeks and them moving up to a full one. Now I've just started taking 2 and I feel so much better and I'm sleeping really good at night. I am finally starting to wake up after 10 hours. I have been having daily headaches and I am thinking it may be the drug. I am hoping it is go away as I get used to it. Anyway, I hope you are still doing well and I hope everyone else finds some hope somewhere.
As the wife of a Cardiologist, it is UNACCEPTABLE for any physician to dismiss what you tell them. The problem was the "Doctor", NOT you. When people find themselves with a doctor that makes them feel misunderstood they should always..always find a new doctor. They're just people like anyone else, and as humans we don't mesh with everyone. Doctors are NO different. Please, find a compassionate physician who is a better fit for you.
Good luck to you!
my doctor diagnosed me with multiple chemical sensitivity disorder many years ago and you're the first one on the fibromyalgia blog that I've seen who has it I would like to hear more about how you're dealing with it and how it makes you feel you can reach me ************ I would really like to find out more about how you live with it and what you do to protect yourself. thank you
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