Solu medrol and pregnancy

Common Questions and Answers about Solu medrol and pregnancy

solumedrol

923105 tn?1341827649 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...
Avatar m tn As far as taking Solu-Medrol with Grapefruit juice, I checked with my eye dr. and my Neuro and they both say that its fine, and actually better absorbed by the liver when mixed with Grapefruit juice vs OJ; although slightly. I have also read several articles by body builders on taking oral steroids with Grapefruit Juice.
Avatar f tn I have just had 2 days of intravenous Solu-Medrol and went to be given the third when I was informed that my body was reacting to the steroids and could not continue. I am swelling all over, it's uncomfortable and not very pleasant!! Has anyone else had this problem and once the swelling goes down are they likely to continue with the treatment?
320873 tn?1253089068 I just got off Solu-Medrol last week and ended up having to have another boost + oral prednisone taper to get me over a flare-up and then a rebound flare-up. I agree with Jason, it is ok to take something to help with sleep as insomnia is a common side effect. Even if you are off it, the effects of such a high steroid dose can linger for a week or two until it is out of your system. Tylenol PM is definitely worth trying.
Avatar n tn 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" ?
Avatar f tn Anyone have any ideas how to cope with the solu-medrol headaches? I slept about 3 1/2 hours, nurse is coming back in 2 1/2 for round 2 of the infusion, so have a couple of more days with the headaches.
Avatar f tn 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!
Avatar f tn lol I did not have any the typical water weight gain ....and I was on steriods 3 months after the solu-medrol ....I was lucky I guess but it did help drinking two glass of warm lemon water a day...it helps flush the system per my neuro dr....
Avatar f tn 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!
Avatar f tn 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.
Avatar f tn I was diagnosed in 2000 with MS, and for years I have been getting IV Solu-medrol treatments every other month, for three days. Is it possible this affects my menstrual cycle? Can Solu-medrol cause not building up the endometrium? Don't worry, I have had all tests: blood, bone density, ultrasound, pregnancy, and I am very healthy: un-pregnant, taking birth control, and so on. I "only" have MS. My period doesn't happen and I am way too young for menopause.
1125401 tn?1262898927 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.
Avatar f tn I finished my IV Solu-Medrol on 9/19, and now only a little over 2 weeks later, my eye is hurting again. Could I already be relapsing? My vision is still o-kay, but the pain is definitely back.
Avatar f tn A week later I had double vision which prompted my first round of Solu-Medrol. The drug did seem to help, and I saw a steady improvement until the beginning of April, where I estimate I was about 95% of normal. Only if I looked to the far left I saw double. Well, I began a new relapse mid April (other sensory symptoms) which I was given another round of Solu-Medrol in the beginning of May.
Avatar f tn 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?
Avatar f tn 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.
559187 tn?1330782856 I am exacerbating right now and again took the Solu-Medrol 2 days ago and am on taper pills now. I am glad I took it again. The symptoms I am having this time are both new and old, though the old ones got much worse. For me, the steroids definitely made a difference in my flares. This time I waited about 3 weeks before caving and taking the Solu-Medrol. It helped me from being pretty much severely debilitating to being able to function better. I don't regret taking them.
450140 tn?1317947304 I finished my last day of Solu-medrol today. I am miserable! Caught a cold, fever, headache. I feel completely drained of all my energy. No appetite, I know right.......Anyone have any suggestons??
Avatar f tn 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.
Avatar m tn 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).
1336491 tn?1340619541 Went to neuro-optho who placed me on three days of solu-medrol (IV) and three weeks of oral steroids (3x day). A year later and still no change in optic neuritis. However, I wanted to know why. Got answer through MS neuro who followed through on tests and uncovered MS. Second symptom showed up two weeks prior to the anniversary of the optic neuritis, pins and needles in feet. Now on Neurotin to help with parathesia. Slows me down a little but it's helping.