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Re: Anyone used Rutuxin?
| J | 17 Jul 2006 18:12 |
> Has anyone received Rutuxin foe arthritis symptoms? My joint pain had > become very difficult to manage and after the FDA approved the use of [quoted text clipped - 4 lines] > frequent episodes of dizziness, light-headedness, I feel like I am > going to pass out after I stagger. Is it hot where you are? I was having those problems on no pain meds.
> I have been able to just hold on to > something until it passes but I am concerned. Any input is [quoted text clipped - 6 lines] > unsuccessful in ever getting off the predisone. Every time we below 6 > mg I experience a full flare - yuck! I don't have Lupus but lots of joint pain. After working (physically) yesterday, I could barely walk nor sit, nor stand for the pain. Joint and muscle pain. I took a Sulindac 200 mg and within an hour, I was almost totally painfree. (some spots did not respond) and I could walk and feel normal again. It's supposed to be for osteoarthritis, but it also helps with me inflammatory joint pains (elbows and shoulders and knees and hips). and some of the muscle pain. http://www.rxlist.com/cgi/generic3/sulindac_ids.htm I do have a history of gastric ulcer, but I take it "with food". Meaning I take some bites, then take the pill, then finish the meal. I also take a gastro med.
I can even sit at the computer now (without pain). Beofre I couldn't.
Ask your doctor if it's worth a try...It's mentioned here http://www.lupus.org/education/brochures/nsaid.html I'll update if any nasty SE's occur. J
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| NorCalLupie | 16 Jul 2006 07:51 |
Has anyone received Rutuxin foe arthritis symptoms? My joint pain had become very difficult to manage and after the FDA approved the use of Rutuxin my Rhuemie started this therapy on me. The joint pain has diminished dramatically but I am concerned about side effects.
About two weeks after the first infusion, I began to experience frequent episodes of dizziness, light-headedness, I feel like I am going to pass out after I stagger. I have been able to just hold on to something until it passes but I am concerned. Any input is appreciated.
I am looking forward learning more from you all. FInding this group on Lupus is new for me. I have been diagnosed for over ten (10) years now and have managed to keep working with the help and cre of my Rhuemie. We have been unsuccessful in ever getting off the predisone. Every time we below 6 mg I experience a full flare - yuck!
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