solumedrol vs solu cortef

Please go back to the doctor and ask for a solu-cortef act-o-vial. You do not want a dex shot as the solu-cortef acts faster and dex takes longer and in an emergency, you want fast. I think as well the dex shots were just recalled. You may have to ask around as not many pharmacies carry injectibles any more but call around and you should be able to find it. My insurance did not cover the emergency shot but last time it only cost $17 so I paid out of pocket.

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.

She told me it is very rare, but not unheard of, to be allergic to steroids. We did skin testing to Solu-Medrol, Solu-Cortef and Decadron. Only the Decadron did not react. So...it is not impossible. I now have my exacerbations treated with Decadron. I wonder if we see this because we with MS tend to get repeated exposure to SM/Decadron. Something I'm planning on discussing with the allergist sometime.

I was very recently dx with MS and have had my first excaserbation in the form of Optic Neuritis. My Eye Dr and Neuro decided it would be best for me to be on Solu-Medrol. I started off with a 3 day course, and the Nystagmus (uncontrollled eye movement) caused by ON actually worsened. At this point, my doctors decided that I needed another 3 day treatment.

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?

My daughter was born with Salt-wasting congenital adrenal hyperplasia, she has developed a Gi bleed at 2 weeks old, corrective surgery at age of 9months, diagnosed with Hypothyroidism at age of 3. Once The thyroid disorder happened she gained weight until she is morbidly obese. We watch her diet, try our best to do what 's right and then last December she had Sinusitis so bad her eyeball looked like it would pop out. Her pressure against her head was +55mmHg.

Hi everyone, I've been dealing with vertigo for the past few days and my neuro wants me to start a solumedrol treatment tomorrow. I've never had this before, so I was hoping you guys could help. I have 2 questions...1) For those of you who have had this treatment before, what kind of a heads up can you give me regarding side effects and recovery time? and 2) Is there anything I can do to lessen the negative side effects?

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.

I started my exacerbation in April of this year and immediately got on Solu-Medrol. I took the Solu-Medrol for 6 days at maximum dosage and tapered off with Prednisone. While my Optic Neuritis went away after only a couple of weeks or so, I soon had a Trigeminal Neuralgia attack. This only happened once, thank God, but a few days later, I began to experience difficulty walking. I still have difficulty walking, some days good, some days really bad, but the other symptoms have vanished.

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.

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 still am thinking Solumedrol is affecting my menses. Had some pretty extensive tests last month, and (gyn) docs are taking a wait and see approach. I had a pelvic ultrasound and then a sono-hysterogram which showed several polyps (uterine and cervical) but not enough to cause any action yet.

So I switched from prednisone to corfef because the prednisone bothered by stomach. The prednisone worked great, but now the cortef doesn't seem to work that well for me. I have only been on it for a few days. Am I feeling weird because the prednisone takes a while before going out of my system? I am wondering if I should have just stuck with the prednisone, even though it bothered my stomach because I felt good on that. Thank you to those who always answer my questions!!!!

25 mg a day vs cortef for AI. One woman in particular has mentioned to me that this has been a great therapy in that she has no highs and lows. I am on cortef due to pituitary AI. And while I have managed to get a pretty good dosing scheme, I still have early morning fatigue. Once I take my cortef I am fine. Is there anyone on the low dose dex therapy that was previously on cortef that has found this to be a better med for you?

My wife has been diagnosed with secondary adrenal insufficiency. This diagnosis was made approx FEB 2007 after many months of Hospitalization. Over the past month she has been getting worse. She was hospitalized 2 weeks ago. Earlier this year she started developing psychosis. At first the episodes were brief, lasting only a half hour or so. Now She rarely gets back to her normal mental state.

m on the Neurology floor of the hospital I work for ina private room, of course (it pays to work in bed management!). I am awaiting my second 1 gram dose of Solu-Medrol no thanks to my (now former) neuro, but rather to my favorite ER doc whom Icalled ahead to make sure he'd see me and would still be working after my afternoon shift. AFter my fave doc started the Solu-Medrol in EC, he made sure it was oredered on the floor. So, here I wait, getting better and better.

He said I needed three days of solumedrol at 1000 mg each day to close my blood brain barrier and selected Tysabri as the MS drug I will be taking. Frankly, I am more frightened of solumedrol than I am Tysabri,JC virus notwithstanding.So far, I have tried to load up on potassium,a few other basic electrolytes and he told me to get some Pepcid ac to protect my stomach lining. he called me and we discussed that part and he said,"now we're ready to roll.

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?

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!

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.

Solumedrol vs solu cortef

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