Solu medrol for copd
Common Questions and Answers about Solu medrol for copd
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Hi twopack, You are absolutely correct about the steroids being of two different types, However, from what I have read, I understand that they are metabolized in a similar fashion. As for Solu-Medrol making joints feel better, this would be the case with reduced swelling, but it looks like I was retaining water pretty heavily, so this is probably where the stiffness and soreness came from.
I was diagnosed with Lupus Nephritus IV , my doctor had me do a 3 day IV treatment of 1g solu Medrol , each, that was a week ago. I was already on prednisone 60 mg a day and right before the treatment Cellcept was added. I am feeling like I got hit by bus ! I read elsewhere that most of my current issues are withdrawal from the Solu Medrol . I was wondering if anyone else has had this treatment and how long it took to feel" normal" ?
Famliy Dr started a Decadron taper saying that it looks like MS but symptoms worsened. Neuro started IV Solu-Medrol 500mg x5 days and today was the last dose. Still numb arm. Just curious if any of you have experienced anything like this or how long it may take to get some relief from Solu-Medrol. Any information is very much so appreciated. Kinda freaking out here!!! Thanks!
I will have my first solu-medrol treatment at the end of this week. I have read the opinion of one person who has had this treatment before and they said that you should not drive or work. It was not clear if they were referring to just hours after the treatment or the entire five day course. I really need to work, and in order to work, I really need to be able to drive. Please tell me your experience with solu-medrol, especially if you continued to work during the treatment course.
I had my first experience with Solu-Medrol infusion in early August. My relapse had just started and was worsening daily-right before I was due to start training for my new job!
The immediate side-effects were quite obvious and well documented. I'm having less success finding out about long-term side-effects-in particular, rapid weight gain. I noticed the bloating quite early in my treatment, especially in my face and abdomen.
Hi,
I am 33 Years old, 7 months back I was masturbating and it seems I pressed too hard on my penis, the day after I felt severe pain on flaccid, I visited a urologist who diagnosed me initially with peyronies disases, and injected me with steroid injection (Solu Medrol 1g), which did nothing with pain. I have done 4 Ultrasounds during the last 7 months and all shows normal. Today I visited the urologist again, and he said there is no fibrosis, it is maybe the dorsal nerve.
Does Solu-Medrol cause bone aching to be worse and what do you find can ease this awful symptom?
All of my MRI's have shown only tiny lesions that are in my subcortical white matter and my doctor has attributed those to my migraines that I suffered in my mid-twenties. I am now 38 years old. But my doc does beleive that I am presenting with "clinical MS".
i had a 3-day solu-medrol infusion last week after a c-spine MRI revealed possible myelitis. i have had all the yucky side effects from the steroids which are subsiding--thank heavens--but instead of feeling better, it seems as though my other symptoms are getting worse--buzzing, achey joints, etc.
is this typical? is it the case where things will get worse before they get better?
I then have to sit for approximately 20 minutes and I can than walk normally again. Last week I went for an infusion of Solu-Medrol. I had one infusion for 3 days at 3 hrs. each. I feel pretty good afterwards and am not limping much at all anymore. My question is regarding side effects of Solu-Medrol. I realize that everyone is different but is there an average time frame for side effects? Today is the 3rd day AFTER the infusions were completed.
I am on day 4 without solu-medrol, but still have the increased appetite..Shouldn't this be going away soon? It's driving me nuts as I worked so hard to lose 48 pounds and sure don't want the solu to blow it. I'm not doing this again. The side effects were awful and the results have not been worth it at all.
I am new to this forum, so not exactly sure how this works. I have had MS for 30 years, been on Copaxone for 8 years and haven't had problems until this Spring. I had a horrible cold, sinus drainage, etc. that would not go away. Dr. gave me antibiotics, didn't help. Then he gave another antibiotic, felt a little better, but still not well. Had a fever for over a month too. Finally I saw a different Dr. and she sent me for a CAT scan that day, I had TOTAL opacification in my sinus.
Other medications are used (like the Solu-Medrol) during attacks, and to help with symptoms (like Provigil for fatigue). There are other medications that are used when the CRAB drugs aren't working, but have risks and side effects (like Tysabri).
On this site, there's a lot of information about medication and treatment, relapses, and pseudo-relapses, etc. in the Health Pages (see upper right hand corner).
I have a friend that went numb from the waist down and although her testing was mostly negative, except a borderline VEP, the neuro told her that he though it was MS and was going to treat her as such. She was given high dose solu-medrol for 5 days and thought she was going to die. All of her symptoms worsened and her whole body started hurting.
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