solu medrol iv side effects

Methylprednisolone is the generic name for Solu-Medrol. We use the shorthand ,IVSM (IV Solu-Medrol) for it on this forum quite a bit.

For those of you who have had to get the solu-medrol treatment IV for 5 days, how did this affect you and your body? It has been a couple weeks since I stopped the out-patient treatment for the IV. I am still awake a lot of the time when I should be sleeping. I got about 2 hours of sleep last night, and today, I lay down to rest and I can't still.

I am on day 5 of 6 now taking this wonderful/awful medication at home (orally) So far it has not been fun, with side effects ranging from swollen hands/feet/joints, pain in joints, weak teeth, high blood pressure, low blood pressure, you name it :) Some advice I can give to those who will be taking Solu-Medrol orally. 1.) Take it with Grapefruit juice, not orange juice. I have read that Grapefruit juice helps your body to more efficiently process the steroids.

I see a lot of people going on solu-medrol lately, some multiple courses within a short period of time. This really concerns me, especially in regards to the potential serious side effects - some which I have experienced personally. My neurologist is very conservative about prescribing solu-medrol He's explained to me that he doesn't give steroids for sensory symptoms like tingling or feeling numb unless it is a new symptom. He orders an MRI to see if there is any change.

After great thought and some research, I decided to go for my first monthly infusion of IV Solu Medrol. I had my whole spine MRI, including the lumbar just recently, and over these years I've probably had the best workup done, as far as the mimics are concerned. So far the MRI of the spine has showed nothing (nothing structurally) and I've never "hit" on any MS mimic blood panel, so I felt comfortable enough seeing what effect the steroids would do.

Debs, It sounds like you mights as well take the Medrol - try it his way and then if it doesn't work out, you can go back and as for the solu-medrol. I'm guessing it is very close- just the "solu" means it is a liquid form (soluble) - again that's just my guess. Sorry you have to tough it out and take the meds - we all are taking stuff we would rather not ingest but do so because we're adults and understand the alternative. :-) Let us know how it goes...

I had a 5 day iv round of solu-medrol from my personal experience I didn't have a problem working or driving to work. ( it might different experience for others) The biggest problem I had for the first two days of treatment I stayed up for about 48 hrs straight so if I need it again I'm going to ask for some type of sleeping aide. Beside the no sleep and the nasty metal taste and very thirsty all the time ...I felt like I could of repainted my house...

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 have the metal taste in my mouth, I could eat my family out of house and home, I can sleep at night fine but need a nap during the day and I can sometimes be very warm or very chilly.

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 have a quick question for you all... My neurologist says he doesn't want to give me Solu-Medrol for this "flare" because he said it would affect the MRI results as well as the LP if we do it fairly soon. Is what he told me true or is he just making me suffer for no reason? I don't know any better and thought who best to ask than you guys. Thanks so much.

I have been prescribed iv solu medrol infusion for 3 days, but after my first dose today I noticed severe leg pain (aching), weakness and some swelling. Is this normal? I still have 2 more doses of the treatment. Has anyone else ever gotten the leg pain AFTER starting the medicine? Thank you.

Technically, any neurological symptom lasting more than 24 hours is considered an exacerbation. Solu-Medrol has proven to shorten the lengths of exacerbations, but has not shown to alter disease course in any way. With that in mind, steroids are completely optional unless there is something life-threatening happening that the steroids may possibly put a halt to. What is life-threatening? Good question, the opinion varies from Doctor to Doctor and patient to patient.

Does anyone have any information on side effects of IV solumedrol? I have taken it before, but that was several years ago. I just finished a 3 day course and today is day 5. I am feeling very stiff and am having much more difficulty walking. Water retention may be a factor, although I am on a low salt diet. I have travel plans next week and am hoping to feel better by then. If anyone has any recent experience with this please reply.

I have just been weaned off of steroids after being on them for a month (MD put me on IV Solu-Medrol every 2 hours when I was hospitalized recently for bronchitis; followed by Medrol Dose pack which did not work, followed by prednisone). The side effects of the steroids were intolerable. When I was on them, I felt better and functioned better, but had horrible insomnia and euphoria.

My question is whether this feeling is a side effect of Solu-medrol or an MS symptom that his not being relieved by the Solu-medrol? I would be grateful for any insight!

Feeling cr@ppy and symptoms are not significantly better 5 days after a 3 day treatment of IV Solu-Medrol. In fact some symptoms are worse , i.e. rib and right leg bone pain; falling in bathroom; complete and sudden urinary incontinence which is now back to urinary hesitancy and urine retention. I don't recall how long it takes to see significant results and I searched some on here before posting.

I have been DX with MS for 4 years now. I am not on any DMD therapy and choose NOT to be. I do not like taking any drugs that aren't absolutely necessary and the harmful side effects of the DMDs made my decision. HOWEVER, I am in a flare (or progression) for the past 2 to 3 months now with may one or two days I felt "nearly normal". I'm to the point of thinking I need relapse treatment. I have Type 2 diabetes as well so steroids can be very bad for that!

Solu medrol iv side effects

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