Guest guest Posted January 25, 2001 Report Share Posted January 25, 2001 melissa takes voltaren 75mgs 2 times a day 2 tylenols 500mgs each up to 4 times a day flexaril 25mgs when needed the voltaren from what i heard has the arthritis med in it along with a pain med the flexaril is a muscle relaxant this helps alot with pain the stressed muscle will cause pain she also takes zyrtec and proventolin inhaler and albuterol solution but thats for her asthma the doctor gave her tylenol #3 but that never helped her at all Robbin Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 25, 2001 Report Share Posted January 25, 2001 , Have you tired Ultram? It works much like narcotic pain killers but isn't supposed to be addictive. At least that's what the dr told me when he gave me the script for it. I do know it is reccommended you do not take it if you have a narctic addiction or have in the past. I'm not sure about the kidney effect though. Arthrtis Inisght has a bit on it and link to other sources. http://www.arthritisinsight.com/medical/meds/ultram.html--- Hendricks wrote:> what meds do your kids take specificly for pain? > not treatment, just pain. > i have tried several with no luck and have kidney> problems to work around. > if you know of anything with really good results,> besides narcotic pain > killers, please reply, brandy> _________________________________________________________________> Get your FREE download of MSN Explorer at> http://explorer.msn.com> > I'm not under the alkafluence of inkahol that some thinkle peep I am. --------------------------------- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 25, 2001 Report Share Posted January 25, 2001 , I took Ultram once and My head felt so strange. I will never take it again. One time a man came into the ER and he was complaining about the way his head felt. He was taking Ultram. So if you try it and your head feel strange at or confused STOP. Good Luck SHU Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 25, 2001 Report Share Posted January 25, 2001 > , Have you tired Ultram? hi waynette, yes i have been rx'd ultram before but i cannot how well it worked for me. i have been addicted to naroctic painkillers before, but it was done on purpose by a surgeon. when my knees were replaced, the pain was more than i could handle and i am not normally wimpy, so they left me on percasette and tylenol #3 too long knowing that it would cause an addiction, but there was no choice. is that kind of addiction you are talking about? i didnt want to take them, i had no choice, the pain of having both knees replaced at the same time was not managable. thanks for your help, brandy _________________________________________________________________> Get your FREE download of MSN Explorer at> http://explorer.msn.com> > > > I'm not under the alkafluence of inkahol that some thinkle peep I am. > > > --------------------------------- > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 25, 2001 Report Share Posted January 25, 2001 > , > > I took Ultram once and My head felt so strange. I will never take it again. > One time a man came into the ER and he was complaining about the way his head > felt. He was taking Ultram. So if you try it and your head feel strange at or > confused STOP. Good Luck SHU > > thanks shu, relafen made me feel like that, brandy > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 27, 2004 Report Share Posted May 27, 2004 Hi Polly, I do not blame you for being concerned about Neurontin. I am on it (but it works well for me), at 900 mgs. per day and I do worry about what it is going to do to me in the long run but I take so many other meds that they probably are doing the same. If the Neurontin gives him too many brain fogs there are other anti-seizure drugs which are effective for Neuropathic and neurogenic pain. I've heard great things about Gabitril, Topamax, and Zonegran all which are anti-seizure drugs but seem not to give as much brain fog as Neurontin. Also tri-cyclic anti depressants help with this kind of pain like Amitriptyline and NOritriptyline. I am on Amitriptyline, 25 mgs at bedtime. Sincerely Ama thepmfarm@... wrote: My husband had asymptomatic spinal stenosis until a bad construction accident/fall. Long story for another day. He was basically losing his whole left side - foot to fingertips. He is now 2 1/2 years post op. Rods and screws in C-3 through C-7. His myelopathy is very bad - the burning sensation on one side of his body just won't quit. The doctors now seem to have basically written him off. And he has been treated at a world-class teaching hospital in Boston, Massachusetts. The main "pain" medicine they have him on is Neurontin. At about 700 mg per day he seems quite clear-headed, but the burning prevents sleep for up to 48 hours until he collapses. At about 900 mg he gets a few hours of sleep every night, but he is really foggy/confused/illogical. At one point he was on approx. 3300 mg per day of the stuff. He is not supposed to drive and I watch him like a hawk all the time. I have SERIOUS concerns about Neurontin. I have had these concerns ever since he went on the stuff. This nerve-pain use of it is "off label". And the manufacturer of Neurontin was just fined $436 MILLION last week for pushing the off-label uses. The only thing it is FDA approved for is seizures. What advice can you give me? Any suggested medications or therapies for the burning sensation? I want my husband back!!!!! Thanks. Polly Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 4, 2004 Report Share Posted November 4, 2004 Hi I am new here but had to reply to this post my husband was put on this Neurontin back in May 2004 he was taking 300 mg 3 times a day and 600 at bedtime he ended up in the hospital in June 2003 due to memory loss he could not find his way home from work it is very scarey thing to go threw Diane > My husband had asymptomatic spinal stenosis until a bad construction > accident/fall. Long story for another day. He was basically losing his whole left > side - foot to fingertips. > > He is now 2 1/2 years post op. Rods and screws in C-3 through C- 7. His > myelopathy is very bad - the burning sensation on one side of his body just won't > quit. The doctors now seem to have basically written him off. And he has > been treated at a world-class teaching hospital in Boston, Massachusetts. > > The main " pain " medicine they have him on is Neurontin. At about 700 mg per > day he seems quite clear-headed, but the burning prevents sleep for up to 48 > hours until he collapses. At about 900 mg he gets a few hours of sleep every > night, but he is really foggy/confused/illogical. At one point he was on > approx. 3300 mg per day of the stuff. He is not supposed to drive and I watch him > like a hawk all the time. > > I have SERIOUS concerns about Neurontin. I have had these concerns ever > since he went on the stuff. This nerve-pain use of it is " off label " . And the > manufacturer of Neurontin was just fined $436 MILLION last week for pushing the > off-label uses. The only thing it is FDA approved for is seizures. > > What advice can you give me? Any suggested medications or therapies for the > burning sensation? > > I want my husband back!!!!! > > Thanks. > > Polly Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 15, 2007 Report Share Posted January 15, 2007 Hello, I wanted to see what the average range of pain medications are. I am currently on Talwin NX every 6 hours and its not cutting it... I'm alternating 4 ibuprofin every 3 hours. I have been on vicodin, vicodin es, percocet, and now the talwin. I am in a ton of pain and dont know what to ask for next. At what point did your docs say " ok its time for pain med mgt docs " and your gp be done with it? and what's the strongest meds your gp gave you? Thanks -- I can do all things through Christ which strengtheneth me Phil 4:13 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 16, 2007 Report Share Posted January 16, 2007 During the worst of my last flare, I was taking 2 Tramadol every 4 hours, with 2 Bufferin every 4 hours halfway in between. I'm down to 1 Tramadol at night only and no aspirin. Tramadol worked very well for me. regards, sherry z > > Hello, > > I wanted to see what the average range of pain medications are. I am Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 18, 2007 Report Share Posted January 18, 2007 In response to > > Hello > > I just wanted to say, I know that nothing I was on in way of pain meds helped at all until I got it under control with the Humira and Methotrexate, no matter what I took it didn't work until I was on the Humira and Methotrexate for about two weeks, and suddenly I was able to cope because the amount of pain I was in was much less than without those drugs, so now the vicadin works. Sincerely, Audrey > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 18, 2007 Report Share Posted January 18, 2007 > > > In response to > <mommytojared@> > I wanted to thank you all for you considerate and caring responses to my post about life after narcotics. I was able to print off all those replies and take them to my Dr. because they said exactly what I have ben trying to say but didn't know how. I am happy to report I am now taking the Duragesic Patch for continuous round the clock pain relief. No more ups and downs from the unsteady levels of vicodin in my sysytem. I have only been on it for 3 days and the differance is so signifigant I can hardly believe it. I am actually sleeping thru the night and able to function much better than I have for years. I am not thinking about pain constantly anymore. I was started on the lowest strength of 25mcg. I change my patch once evry three days so it's really nice not having to think about controlling constant pain! I hope this post helps somebody who might be stuck in the same vicious cycle I was in. I am now able to stay much more mobile and that also helps slow down the progression of this disease. I feel like I am getting my life back and thinking more clearly. I wonder if some of our brain fog and fatigue comes from constantly fighting and being in pain? It is hard to get your mind on anything when your are so aware of the pain. Again thank you all so much. I don't know if I would have had the courage to talk with my Dr without your support. I feel I was sent to this group for a reason and I hope others can have this same result...Thank you, Shaw Quote Link to comment Share on other sites More sharing options...
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