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[i]I was prescribed neurotin almost a year ago for pain in my right leg. The think the nerves are pinched from my disc fusion in 2000. I had no idea of all these side effects. I'm not quite sure about the memory lost part of it. Can anyone help me on that. I'm tired all the time and yes the shaking of the hands. I also take ultrum with it. A pain killer. I hate the way it all makes me feel. Always tired and a lot of the time I feel sort of out of it. Can anyone help with all the side effects of this drug that of course your Dr.'s don't tell you.
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EXACTLY... I was on the Neurontin/Ultram combination for two years. I have Trigeminal Neuralgia. Let's see... overwhelming sleepiness, couldn't even keep my eyes open,... was physically sick if I tried to move too quickly (meaning more than a crawl)... could not even walk further than about 10 feet after a while on the meds... I cannot even describe the loss of strength I experienced... I was a gymnast and used to being stronger than most women, but I became so weak I could not even pour my own milk... shaking hands you say?... could not stop my whole body from convulsing; and, even today, two years after going off the meds, my hands still shake. What else? Hmm... horrible dizzyness, VERY low blood pressure, seizures, and major depression. I attributed the depression to the fact that I was sick until I stopped taking the meds and realized that I my normally positive outlook was returning slowly.
As far as the accusations about Neurontin being linked to Suicide... that is not difficult for me to believe. Before I went on the drug, I had a very definite opinion about the value of the life God had given me and the tragedy it was that people who took their own did not see the possibilities of the future. Even having that as my core belief, I have to confess that after I had been on the drug for two years, my mother had to pick me up off the floor (both of us crying) because I had told her that I did not think I could face another day. The only reason I am still here is because of the strength of my core beliefs and my faith in God. I attributed my deep depression to the overwhelming difficulty that accompanies the pain of Trigeminal Neuralgia (and every other dibilitating illness... loneliness, financial distress, loss of prior goals, dreams, and lifestyle etc...)
Anyway, I deal with my disorder now without medication... and, Thank God, it has become much more bearable over time. I am young for a Trigeminal patient, and at some point I realized the drugs were killing me and making my life worthless. My advice to you is to take as little of whatever they (meaning Dr.s) give you as possible and seek out every other mean of alternative medicing available to you. I have found that a medical massage once or twice a week makes a HUGE difference in the quality of my life, so when I was able to start working again, I was working solely to pay for that! :-) Now, I am doing very well... healthy enough to handle, successful in my challenging business, and strong.
One more warning about those meds... they take a LONG time to get out of your blood. It took me over a year after I stopped taking them to not feel like I was going to faint all of the time. The dizzyness and the hand-shaking still persist to this day. And just to give you some vitals... While I was on those meds, my resting heart-rate (first thing in the morning) fell to 37 beats per minute (off from the 55 before the meds) and has only come up to 42 since then. My lowest documented blood pressure was 84 over 47... rediculous! A forced glass of red wine every night helped bring that up, but I will admit that I have no idea what the reading is now.
Okay, I wish you all the best. I wouldn't wish these symptoms on my worste enemy!
I forgot to comment on the memory loss issue. I have been complaining about my loss of memory for the past 3 years, but I do have good news with regard to that. My memories are returning... not the ones from the time of my illness, but I am definitely remembering more of the time before I started taking the medication. They are all coming in unexpected and much valued flashes that develop quickly into full memories upon reflection. I very much appreciate the clarity of them because that is really what was missing for so long. I was worried that I would not get my memories back, but I have high hopes now that they will all be restored in time.
As far as the memories I lost from the time I was on the meds... those are really difficult to conjure... sometimes seemingly impossible. I had to look up my original neurologists name on the internet today because I could not remember who he was... not typical for someone with a brain like mine. Before I got sick I had a 4.0 at Columbia University. I joke now that I spent $100,000 on an education I can't remember. :-) Hey, maybe there is a lawsuit there! :-)
Hi stefanijall. Great post
for all. One year-- that explains alot right there. I especially like your memory loss one, because that is what I still have symptoms there. But my memory loss will come back 1 o2 days later at the wiederst times, whether in a dream or driving in my car. I have faith your college education won't be lost. Thanks for the two great posts. Encouragement for all!
8)
Aloha Skooze
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I only used Neurontin for 3 months. My memory left, I wanted to sleep all the time, increased appetite, was dizzy all the time. I was afraid to drive. I stopped taking it Oct. 3. Since that time I have times when I can't sleep at all, other times I want to sleep all the time, my appetite is still crazy, am still dizzy. The day after I stopped taking this my entire body was screaming at me! I am depressed although I have not thought of suicide at this point. People that know me are concerned about what is happening to me. I am becoming anti-social and at times argumentative. My personality is changing right in front of my face. Is all of this normal? Can anyone tell me how long it will be until I 'find myself' again or will I? I called and told my Dr. I was not taking it any longer and why and he said it was a good idea I quit!
I was prescribed Neurotin for several months as a pain med. I experenced memory loss, weight gain, and slurred speach to name a few. About a month ago, I had my first seizure. Now I am terrified of what this may do to my future. I've never had any head injuries or neurological problems. I was prescribed this med for pain because of an injury to my shoulder, I had no idea it was actually anti-seizure medications. Could this in any way have lead to me actually having a seizure? And now that I've had a seizure, does this mean I'll have to stay on meds for the rest of my life? Please help!!!
My CNP talked to me today about the above medicine. She is using this on some of her Fibromyalgia patients for pain and this is what I have. In reading these posts I don't think I want to try this Rx. I already have enough memory loss. thank you!
I'm so lost is there anybody out there ??
I'll give it a little while longer, but not holding a lot of hope just another dead end.
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I was prescribed Neurontin 1200mg per day to try to restore nerves in my left leg damaged in a fall. Over the six months I was on it, I gained 50 lbs, and lost my job as the master picture framer for a company I had been with for over ten years due to incompetence. This drug made my thinking so fuzzy I couldn't function in a professional capacity, and it came on so gradually, I didn't realize what was happening until I lost my job and my reputation.
I realize that the survivors of those unfortunate people who committed suicide are more deserving of being included in the class-action suit than those of us who simply lost careers, but it should be otherwise, and the suit should be expanded to include us!
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I was prescribed Neurontin (Gabapentin) 300 mg. twice a day. My Dr. has prescribed it for Headaches. I have had them all my life. I started taking various different meds at an early age to try to eliminate headaches. I have been to many Dr's. all of them focusing around "migraines." Neurontin is just another med. used for headaches, (migraines in particular). MY pain ALWAYS starts in my neck, as I have several vertebra that are pinched and cause constant pain. Headaches are a daily issue. I have tried EVERY alternate form of pain therapy ( chiropractic, message, acupuncture, potassium, many different herbals, Prolo therapy, etc...) nothing works. Neurontin, makes me dizzy, tired, and when I get up in the night to use the bathroom, I see things, shadows that move. Has anybody experienced that? I am not going to take this anymore. I'm 48 and want my 17 year old body back!!!!!!
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I had 2 cervical fusions, one in 1996, the other in 2001. A plate was installed in the latter. C3, C4, C5, C6 and C7 are all fused. Each fusion was prompted by ruptured discs and both incidents caused damage to my spinal cord as bone spurs cut into it. I fell several times after the last fusion which caused spinal cord edema and caused more damage. Afterwards I was left with a multitude of symptoms including severe lower back pain, a feeling that my body cavity was pressurizing as I walked, and a feeling that the underside of my arms had all the skin scraped off from my wrists to my elbows. My shirt sleeves touching my arms was maddening as was water from a shower spraying on them and even air from the dash vents of my vehicle blowing on them was painful. I was in so much pain that even sleep was impossible until exhaustion would set in and I'd nod off. (I had a complete spinal MRI done about a year and a half after the last surgery to ensure nothing else was amiss. Nothing was found.) I was started on Oxycontin for the pain and it really helped. My mobility returned without walking around feeling stoned. I had my dose gradually raised until I was at a state where I still hurt a bit, but I could do all the necessary things to live a somewhat normal life. Current dose is 60 mg 3 times a day. However, the Oxy did absolutely nothing for the feeling in my arms. That provided my introduction to Neurontin. I was originally taking it 4 times a day; 300 mg 3 times and 600 mg at bedtime. It helped the burning. I still felt it, but it had lowered in intensity to that of a bad sunburn. After a couple months on it I started having trouble with throwing up a little bit in my sleep and an awful medicinal taste would be left in my mouth that brushing and gargling wouldn't take out. I reduced my Neurontin dosage to 300 mg three times a day and still had the same pain relief as I had on the higher dose. The puking up ceased. When I saw my neurologist at the next quarterly office visit I told him what I had done, and why. He was OK with it. Meanwhile I had started having severe leg cramps in my calves. It was both Charley Horses with knotted muscles and unconsciously bending my feet down as far as they would go and continuing to force them down. When I would get up in the morning I could hardly walk my calves would be so sore. I would walk like I had swim flippers on. The cramping spread to my forearms and fingers and would be so excrutiatingly painful I would actually start crying out in pain. They would come at random in that I didn't have to be doing anything to trigger them. Sometimes just trying to hold a pen and write would make my fingers go into painful spasms. These would sometimes go on for hours. When I walk my feet curl as I lift them so I would step down on the outer edge causing me to twist my ankle and fall, or just fall. My knees occasionally buckle without warning sending me down. My balance was easily upset and trying to recover it was an exercise in slapstick comedy as I would pitch this way and that, each movement an overcorrection for the last overcorrection until I'd fall. My knees hurt so bad I hate having to kneel down. Picking up something off the floor requires a movement in which I aim at the object, align my arm down my side, then I squat as rapidly as possible, try to grab the item and try to utilize the momentum of the downward motion to create a bounce to help stand me back up again. All my doctors have blown these things off and offered no recommendations to help with them. Recently I saw one of my neurologist's partners while he, my regular doctor, was out on medical leave. This guy never asked me a damn thing about my condition or my lifestyle, my job, or anything. He treated me like I was a criminal for taking Oxycontin and said I wasn't taking enough Neurontin and "we" could go as high as 5000 mg a day! He changed my dosage to 2400 mg a day from 900 mg. I've been on the higher dosage for about 10 days as of this writing. I spent the first 3 days so tired I had to hide out at work and sleep because I couldn't stay awake. I couldn't carry on a conversation without forgetting what was being talked about in mid sentence. I couldn't do simple arithmetic in my head. Since then the fatigue has subsided, but some days it comes back. I have no energy and just want to lay around. My stomach has been upset, the cramps are just as bad. I feel weird all the time in a way I can't explain other than I just don't feel right. I sleep all night and wake up feeling more tired than when I went to bed. I have bad dreams every night. I have started having cramps in my rib cage. Worst of all, this insidious feeling of hopelessness is creeping into my conciousness. I find myself wanting to give up because this whole thing with my health feels so pointless. I KNOW that's not me, but I am losing my conviction that I'm stronger than that. I'm scared because this new reality is spreading and this doctor won't listen. I'm only half-way to what he said he wanted to go to with the dosage he put me on. His concern seems to be solely getting me off the Oxycontin and nothing else matters. Not my quality of life, not my ability to continue to provide for myself as I have done my entire life. I told him I didn't give a damn what medicine I took- all I want is relief so I can live as normal a life as I could. I am 51 and probably don't have a lot of years left anyway. I sure would like to live them normally. But, I don't know what direction to take. All ends seem to lead to a bad place.
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[quote]I had 2 cervical fusions, one in 1996, the other in 2001. A plate was installed in the latter. C3, C4, C5, C6 and C7 are all fused. Each fusion was prompted by ruptured discs and both incidents caused damage to my spinal cord as bone spurs cut into it. I fell several times after the last fusion which caused spinal cord edema and caused more damage. Afterwards I was left with a multitude of symptoms including severe lower back pain, a feeling that my body cavity was pressurizing as I walked, and a feeling that the underside of my arms had all the skin scraped off from my wrists to my elbows. My shirt sleeves touching my arms was maddening as was water from a shower spraying on them and even air from the dash vents of my vehicle blowing on them was painful. I was in so much pain that even sleep was impossible until exhaustion would set in and I'd nod off. (I had a complete spinal MRI done about a year and a half after the last surgery to ensure nothing else was amiss. Nothing was found.) I was started on Oxycontin for the pain and it really helped. My mobility returned without walking around feeling stoned. I had my dose gradually raised until I was at a state where I still hurt a bit, but I could do all the necessary things to live a somewhat normal life. Current dose is 60 mg 3 times a day. However, the Oxy did absolutely nothing for the feeling in my arms. That provided my introduction to Neurontin. I was originally taking it 4 times a day; 300 mg 3 times and 600 mg at bedtime. It helped the burning. I still felt it, but it had lowered in intensity to that of a bad sunburn. After a couple months on it I started having trouble with throwing up a little bit in my sleep and an awful medicinal taste would be left in my mouth that brushing and gargling wouldn't take out. I reduced my Neurontin dosage to 300 mg three times a day and still had the same pain relief as I had on the higher dose. The puking up ceased. When I saw my neurologist at the next quarterly office visit I told him what I had done, and why. He was OK with it. Meanwhile I had started having severe leg cramps in my calves. It was both Charley Horses with knotted muscles and unconsciously bending my feet down as far as they would go and continuing to force them down. When I would get up in the morning I could hardly walk my calves would be so sore. I would walk like I had swim flippers on. The cramping spread to my forearms and fingers and would be so excrutiatingly painful I would actually start crying out in pain. They would come at random in that I didn't have to be doing anything to trigger them. Sometimes just trying to hold a pen and write would make my fingers go into painful spasms. These would sometimes go on for hours. When I walk my feet curl as I lift them so I would step down on the outer edge causing me to twist my ankle and fall, or just fall. My knees occasionally buckle without warning sending me down. My balance was easily upset and trying to recover it was an exercise in slapstick comedy as I would pitch this way and that, each movement an overcorrection for the last overcorrection until I'd fall. My knees hurt so bad I hate having to kneel down. Picking up something off the floor requires a movement in which I aim at the object, align my arm down my side, then I squat as rapidly as possible, try to grab the item and try to utilize the momentum of the downward motion to create a bounce to help stand me back up again. All my doctors have blown these things off and offered no recommendations to help with them. Recently I saw one of my neurologist's partners while he, my regular doctor, was out on medical leave. This guy never asked me a damn thing about my condition or my lifestyle, my job, or anything. He treated me like I was a criminal for taking Oxycontin and said I wasn't taking enough Neurontin and "we" could go as high as 5000 mg a day! He changed my dosage to 2400 mg a day from 900 mg. I've been on the higher dosage for about 10 days as of this writing. I spent the first 3 days so tired I had to hide out at work and sleep because I couldn't stay awake. I couldn't carry on a conversation without forgetting what was being talked about in mid sentence. I couldn't do simple arithmetic in my head. Since then the fatigue has subsided, but some days it comes back. I have no energy and just want to lay around. My stomach has been upset, the cramps are just as bad. I feel weird all the time in a way I can't explain other than I just don't feel right. I sleep all night and wake up feeling more tired than when I went to bed. I have bad dreams every night. I have started having cramps in my rib cage. Worst of all, this insidious feeling of hopelessness is creeping into my conciousness. I find myself wanting to give up because this whole thing with my health feels so pointless. I KNOW that's not me, but I am losing my conviction that I'm stronger than that. I'm scared because this new reality is spreading and this doctor won't listen. I'm only half-way to what he said he wanted to go to with the dosage he put me on. His concern seems to be solely getting me off the Oxycontin and nothing else matters. Not my quality of life, not my ability to continue to provide for myself as I have done my entire life. I told him I didn't give a damn what medicine I took- all I want is relief so I can live as normal a life as I could. I am 51 and probably don't have a lot of years left anyway. I sure would like to live them normally. But, I don't know what direction to take. All ends seem to lead to a bad place.[/quote]
I need not post with my small issues with headaches. You and others on this posting site are the real soldiers. I just have bad headaches. I can still do everything, Ride motorcycles, karate, dirt bikes, etc...I can even do the splits. Some of my headaches are painfull enough to make me puke, but I now consider myself very lucky. My hat goes off to all of you. Drs. do want to prescribe lots of drugs to mask the problem insead of finding out alternate ways to efliminate to root.
GOOD LUCK ALL AND KEEP YOUR CHIN UP.
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Wow... I have never really thought about what these drugs can do to you.... I mean, I was just blindly taking any pill the doctor gave me..... I was prescribed Neurontin about a year ago and was on it for about six months.... They gave it to me to help with the pain in my legs after a spinal cord injury... I have been reading aobut all these side effects like memory loss, aterations in sleep patterns, depression, and others.... and I know exactly how you guys (and gals
) feel... I actually tried to complete suicide right before taking myself off the drug.......And since then.... I have the worst short-term memory in the world..... I am always tired, but can never sleep... I am just glad that there is a place where people can come and talk about these types of things...... I think I have said enough for now though.....[/color]
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i am sick of medicine. i am a forty-nine year old woman that is dealing with fybromylgia for the last fourteen years along with arthritis,two different kinds and dealing with diabetes. i also have high cholesterol. i have tryed all the pain meds. and nothing seems to work. i also took neurontin my dr. started me out taking one three times a day until i got up to twelvehundred mg a day, i was walking into walls crying all the time didn't care if i lived or died. iwas always tiried but couldn't sleep my family didn't understand they just kept saying maybe it's the medication your taking all i know is that i hurt i would have tryed almost anything to stop the pain. sometimes i would set up at nite and just cry and think that i didn't want to live anymore. i stayed on neurontin for about fourteen months and i would never go back on it again, you don't know how bad it was for you until you get off it and you can start to think again. i still have alot of pain everyday and take other pain meds that don't work very good either, there is days i can hardly move and it makes it hard to keep going ahead. as if i didn't have enough problems my dr. put me on a drug that just about killed me. he said that my cholesterol was to high so he put me on crestor 10mg. at bed time, i only took it for six nites after the forth nite and the next morning i went to get out of bed a fell into my bedroom wall due to severe cramps in both of calf. i though i had just bruised my shoulder but the pain never went away it only got worse and my arm keeps getting stiffer so my dr. finally order a x-ray and a mri. just to find out that when i fell i tore my muscle and tendon up to the shoulder. i now have to go get hooked back togather i only hope they can make it right. to every one out there please research the drug crestor if your dr wants to put you on it, my personal though is i wouldn't and will never take any drug to lower my cholesterol i also had trouble with lipitor and tricore that caused severe pain in the legs and all three drugs left my legs and arms week and in alot of pain. crestor caused severe cramping and after only six days of taking it.
good luck and god bless
rose
tsvjmv7784
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I am so glad I found this forum - now at least I know I am not
alone. My surgeon gave me this "wonder drug" after fusing my spine with two rods and eight screws and bone from my hips. Our pharmacy did not have any in stock and my husband was told that he had to find it - that I would not be able to stand the pain without it - there was no mention of side effects!
I was up to 3600 mg of neurontin daily in addition to pain killers, muscle relaxers and meds for depression - from what my family tells me - I was a basket case. I do remember sitting on my bed at night rocking - not wanting to live. I remember falling all of the time and I also remember trying to jump out of my daughter's moving truck - that was when I started to take myself off of the drugs.
I have been off neurontin for almost two years now and I still have major memory problems - both long and short term. My kids will talk about things we did when they were young and I just can't remember - I will read a book or go to a movie and
not remember much about it.
Does anyone know if there has been any testing done to see
if the damage caused by neurontin is permanent? I read one post where someone is started to get some of their long term memory back - I would like to think that this is possible - sometimes I feel like an outsider in my own life.
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Thank you all for your stories. I have recently had my peripheral nerves and right arm tendons damaged due to Levaquin and, after meeting with the neurologist yesterday, he prescribed Neurontin for the nerve pain. Thank goodness I had the sense to do research before filling the prescription. I find it appalling and just plain hard to believe that this dr. prescribed Neurontin as a first choice of action. I was quite clear with him that I tend to be the patient that will manifest with the "severe reactions" listed on the data sheets. He assured me that this is a very safe drug that is well tolerated. Well this was EXACTLY what I was told about Levaquin and now I can no longer hold a coffee cup after only 2 doses of that drug. I keep thinking about all the folks that aren't aware of their options and don't have access to or knowledge of the internet's availability of info. Too many lives are being damaged by the quick and easy dispensing of drugs that are too little understood. Good luck to you all and best wishes for continued healing.
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Wow, I am amazed that any Dr. would prescribe this to someone! My mother in law is like a child on crack when she is on this! She doesn't remember my husband (her son) or any of her daughters unless they say say something Like "ma it's "so and so". It's the craziest thing I have ever seen! She's like a zombie sometimes and other times She giggles and snorts, she can't walk, she thinks the Green Berets are after her!! I am terribly disturbed that her doctor gave her this! I sent these comments to my sis in law so she could read them and talk to her (mom in law) Doctor about finding some other pain reliever.
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I would suggest you go to: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?CMD=search&DB=pubmed and post key words relating to your problem. Abstracts to journal articles therein may help you. Good luck.
Harold Boxenbaum, Ph.D.
www.arishel.com
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Trying to behave , thought I would see if anyone understands . It seems like I put myself on a blacklist in Kansas for legal aid , and I can`t really blame them . I so complicated my case , as I really have no case at this point in Kansas . I have A January hearing , again , but I dont know how to proceed . I`m trying to share the responsibility of my condition , not even sure what that is , to include Pfizer . Wanting to amend a workers comp claim against Boeing to include Pfizer as a respondent , and to get the case to another jurisdiction possible , hopefully out of Kansas , if possible . How does one make a case for suicidal tendencies if they are still alive ? I was put on 3200 mg of Neurontin for 7 or so years , ending in 2004 . Seems every motion I make or appeal I try just makes every attempt at fairness worse . Unable to stand without shaking , sit without twitching , or sleep without waking every hour or two , I`m written myself off as the guilty party for allowing myself to eat all the meds prescribed for me over the last 10 years . After losing my 17 year job for inappropriate behavior , as they say , I am still alive . 4 months before I was fired , I had carpal release on both hands . Within a week after opening a new work comp case in 2004 , I no longer had a job , unemployment was denied , and severance was denied . My ex doctor wont see me anymore , reduced the bill I owed from 300 or so to 15 last week , but will not reply for my request for assistance mentally or physically . Somehow , a year after I was terminated , I was given SSDI , without appeal , but I dont even know for what , except they say I`m severely depressed . I gave up a few years ago , but I wake every day wondering how to prohibit these drug companies from pushing some of there so called wonder drugs . Thank you for allowing this , if it is allowed , just so used to hearing my case , and my life , has no merit . Paul
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Hi!! I take Neurontin 2400 mg /day for the symptoms of RLS ! Anyway this med was supposed to help with the symptoms and so far it has not!! I am like a drunk walking around the house with RLS!! I also awaken every 1-2 hours when I am able to sleep! I`m going off this med ASAP!! But since I have tried all of the others including Dostinex and now I have cardiac valvular disease from that med!! There really is very little choice in the available meds left for me to try! My next step is a narcotic! And I do really hate to take that but I also am very desperate for a good nite`s sleep too!! Anyone have any other suggestions that they might share!!
Diane
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Hi, All! Just found out my surgery has been put on hold! Seems like the "flex rods" they were going to put in are going to be or already have been taken off the market because they are having problems with them breaking! I was offered to have surgery,(minus the flex rods) to relieve my suffering,but now, I just don't know what to do! Any suggestions? As long as I stay on my regiment of patches,Percocet, and Neurontin, I can manage the pain EXCEPT for the times when only morphine helps! And theres another problem! When I go to the E.R, I get treated like I'm a junkie lookin' for a fix! So, most times when I really SHOULD go,I don't! I really don't want to have the surgery without the flex rods,because I feel it's like putting a band-aid on a bullet wound! I'll just have to go in again to have it fixed again...and again...and again! Help!
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