solumedrol by iv

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 had a 4 day Solumedrol drip and then step down pack in February and it made me worse. All my muscles tightened up and I have more pain than I did before. Call it a major fibromyalgia attack. Even now in May, I am still as stiff and woozy as i was after the glucocorticoid therapy. Sigh. Did nothing for me that I can tell. I did sweat a lot during the treatment so maybe i lost a few toxins?

t help, so I had the 3 day mega dose IV solumedrol. I did not do the tapering off pills, because I was having a reaction to the medicine. Since the end of February my ankles are swollen everyday, all day. I asked my neurologist, and she said it is a side effect of the solumedrol. Any one else experience this.....swollen ankles for so long? When will they return to normal? Help please. Thank you.

My understanding is (and hopefully someone will correct me if I'm wrong) that IV solumedrol is of the most use within the first weeks of a relapse. In the area where I live, steroid use for relapse is waning. There is quite a bit of research showing the in most cases, the relapse length is only marginally shortened. Given the risks (blood sugar issues, bone density changes), steroids are no longer given automatically. I would consider it if I lost vision.

I have been told I am going to get started on a 3 day course of IV steroids. I would like to ask those of you that have had this what they felt like during and after they had it? Did anyone have any adverse side effects? Did you feel they helped reduce the flare up?

I am 9 days out from getting 5,000 mgs. of IV SoluMedrol. I have had more results from a dosepack than this massive amount of steroids. It did make the inside of my mouth & lips swell and my throat felt like I was breathing fire. Gol bless MD Anderson. I wasn't able to eat either. I have RA, MS, Meniere's, and Also, if anyone out there has both RA and MS, would you please share what treatment regime you are taking? Soft hugs to all and Thank you in advance.

coming with hat in hand is how in te world do ones manage the bizarre psychotic type side effects from the IV solumedrol? I just finished yet another five course today and frankly I had hugs melt down scared my caegiver.. and fnally made th eprimary car e doc understand thath 72 hours of mania, depression, wailing, and all that jazz was no acceptable. This is the first time I have dome them in a home setting versus in patient..could that be afcator? or am I just a little nutty...

i have a PICC line as I have been going through a 2 mnth relapse with my MS and I finally gave in and went to the hospital....of course it is solumedrol pumping through it but its way different than when I had an IV port last year...question though; I feel so dizzy and have feelings l want to pass out at times even though I don't pass out. is it because of the PICC with solumedrol that is giving me a different experience?

ve had a horrible experience with Solumedrol as well.....Back in March I had extreme leg and groin numbness and went on IV Solumedrol for 3 days....I had a nasty reaction to it, but it DID take away the numbness and vision problems almost immediately....Well, within 48 hours anyway..... In May the left side of my head and face went numb and because I was visiting the MS Clinic at that time, I declined the Solumedrol treatment.....That numbness didn't go away for 20 days.....

ve only had one relapse, a year ago which resulted in my MS diagnosis, but I was hospitalized for the 5-day IV Solumedrol. It was 4 x per day -- every 6 hrs. The reason for the hospital stay was the need for round-the-clock infusions (no infusion center available at all hours), PLUS Solumedrol can raise blood sugar to dangerous levels, so I had blood sugar tested every 4 or 6 hrs -- got up to 145 once, and 130 twice (I'm not diabetic). I was given insulin shots then.

I am scheduled Monday to do an IV for three days of Solumedrol. Has anyone else done that and if so, what is your opinion. I am alittle nervous about it.

These are the same problems I have with Solumedrol. Diabetics have a hard time with Solumedrol and it seems that insulin or diabetic pills, cannot work hard enough to get high blood sugar levels down. Here where we live in Virginia, they will not do a treatment, if your blood sugar level is about 200. This is a good drug, but very hard on someone that is prone to high blood pressure and high blood sugar.

his office just called and wants me to take 1 IV treatment of solumedrol - equivalent to 1 gram of the medication. they said if my symptoms improve, this could be more evidence of MS....if they do not improve, then maybe not MS. my concern is that my symptoms aren't very strong and i don't know if i would really notice a difference...or maybe i would? geez, can you tell i am a mess about almost everything! so, have you done this?

I had IV Solumedrol in Oct. 2006 and again in Feb. 2007. In October, it was the most wonderful feeling to be able to function without pain again. My eye improved 100% and I felt good through it all...the downer was that it only lasted until February 2007. My symptoms from the Paratrigeminal Neuralgia came back, my eye drooped and the icepick restarted it's attack on my head. I had Solumedrol IV again for 3 days and felt great again other than the horrible taste in my mouth...

I just finished my first SoluMedrol IV bag. The lights are so bright! Has anyone else experienced this?

I just finished 3 days of IV Solumedrol.. I feel horrible, swollen painful lymph nodes in clavical, cerevical and back of neck, my ears hurt ...Has anyone ever had this after solumedrol? I have done solumedrol before but do not recall ever feeling this poorly.

m sorry you have joined our ranks. If the doctor is doing IV solumedrol with the orders for MS, then it sounds pretty sure to me too. At this point you need to go back to the neuro and sit down and discuss treatment options. All of these symptoms you describe could be from the MS and the neuro is the right source for information. It is hard not to panic when you get this dx. Alex is so right .... breathing is essential.

So today is 2nd day of solumedrol, plus about 3 other IV meds, for migranes and nausea. Tomorrow is my last day, and it will b 6 hours. As I am in the middle of the infusion, my PCP calls, and tells me my chest xray from yesterday shows pnemonia. Ok, so solumedrol with pnemonia.. I am no doc, but pretty sure that is not a good mix. I started with this chest infection about 5 days ago. Always something. I need to sleep, that might help.

t been on in a while because I had an exacerbation from the flu shot. Then, Dec. 5 I started IV soluMedrol at home. Nurse came every day and infused me for 3 days, then a nurse followed up with my sugars, etc. for another 4 days. It was great..only way to do it. Ah, but then it gets even better. On Christmas Eve, my family came over and my grandson either had a cold or the flu..By the next night I was sick..Wound up in the hospital January 2 with pneumonia and more soluMedrol..

Solumedrol by iv

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