Solu medrol vision

Common Questions and Answers about Solu medrol vision

solumedrol

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 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.
1336491 tn?1340619541 Hi Jan - Just a few words on my personal experience with solu-medrol. I was on a 5-day infusion for loss of vision. Took a month afterward before I started to see results, but who knows if it was b/c the steroids or natural wane?... Next time I had the 5-day infusion was in March for heat band and down my leg. Felt better after 2 weeks.
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...
320873 tn?1253089068 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.
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" ?
559187 tn?1330782856 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.
Avatar f tn i had on hand a solu-medrol had my boyfriend give me inj 1.5cc Im glute but he gave it too me about 1 inch to the left and now i have swelling at the site about the size of a quarter i am a nursing student and try to walk him through it and made sure he aspirated will i be ok???
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.
559187 tn?1330782856 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.
Avatar m tn I am bumping this up in hopes that Quix or Cobob see this. I do know it is important that your neuro is aware of the problem. They do usually get IVSM into ya pretty quick with it.
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 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.
Avatar f tn 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.
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.
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.
703392 tn?1228522962 During her episode of ON earlier this year, she was on the IV solu-medrol again, and also on a slow taper of oral steroids. At present, she is suffering through a bad cold and I'm hoping it will not lead to ON again. Thanks again!
Avatar m tn Then He said “we need to inject three injections(Methylprednisolone sodium succinate for injection USP – SOLU-MEDROL 1gram)”. We agreed and he did injections and multivitamin injections also. Right Now He did not get vision for left eye.
Avatar f tn Hello! Sorry your son is going through this! I just wanted to share with you my experience! I had a successful decompression! But I have had to deal with horrific side effects. Since the surgery I have dealt with a lot of headaches. With the right dr and with time I'm learning to find the triggers and a lifestyle change to avoid them. I am not going to lie....it's a big lifestyle change and not a lot of fun! Initially he diagnosed it as migraine headaches.
Avatar f tn I HAVE BEEN ON STEROID INFUSIONS MARCH 2007,JUNE 2007,OCTOBER 2007,DECEMBER 2007 AND MARCH 2008,PLUS I HAVE HAD BOUTS OF ABSENT VISION FROM OPTICAL NEURITIS AND MY NEURO WILL TREAT THAT AGRESSIVELY WITH 1500MGS OF SOLU-MEDROL IN 15 MINUTS HE HAS DONE THAT TWICE NOW. THE INFUSIONS ARE GREAT IN REDUCING THE IMFLAMATION,BUT TO BE ON THE SAFE SIDE PLEASE CALL THE HOSPITAL.
Avatar n tn I was diagnosed with MS due to the eye pain and blurred vision via an MRI, Optic Neurtis. Did the 3 days of Solu-Medrol and I had NO improvement. Had my last IV dose 9 days ago, no taper. I have read that most people have immediate improvement. Can anyone help? Was diagnosed 2 weeks ago and I am still a mess over this. Was laid up in bed for 6 days due to the spinal headache and failed blood patch.
324913 tn?1302869517 Hi everyone. I'm new to this forum on medhelp and would really appreciate opinions on people in the know as I'm on my 2nd day of a my first 3-day run of Solu-Medrol (1000mg) and am a little concerned. I've read lots about the various side effects but I'm still not sure about what's going on with me. I'll try to keep this short but a brief history. 1st attack - 1997 - numbness in extremeties and my skin was numb all over from the neck down. Lasted about 5 weeks.