Solu medrol symptoms and conditions

I was prescribed generic Wellbutrin two weeks ago today. I took it for 10 days with no problems except mild headache, mostly pressure. I felt great even after only 10 days and had tons of energy. I know it usually takes 3-6 weeks for the full effects but I was already happy after only 10 days. I thought this was a miracle drug. On the 11th day I had a few hives on my inner thighs and on my chest but I didn't think too much of it. On the 12th morning I had tons on my thighs, entire torso from abdomen to chest, shoulders upper arms, neck and back. I even took pictures to show my doc of the ones of my back. I tried to get in touch with my doc which was this past Wednesday 5/27/09 but his office closed early that day. I then called my pharmacist. He told me to go to the ER immediately. He asked if I was having shortness of breath and I told him I couldn't tell if it was related to meds because I am prone it anxiety and I was a bit anxious about the hives all over. I went to the ER and they gave me a shot of Solu-Medrol (a steroid) in the hip and but me on a steroid (prednisone) pack for 6 days. I only took the prednisone that Wednesday night. Yesterday (Thursday the hives were visible but soo much better, and today (Friday) they are completely gone. I am so disappointed that I had this reaction because I loved taking buporion (generic wellbutrin). I wonder if it's just the generic that does it because I read someone else say that the name brand didn't give them hives but the generic did. I will have to check in to that. The ER doc told me to stop taking so my last does was Wednesday morning. (ohhh by the way I was on 150mg once in morning and once at night, so 300mg/day and I was on the wellbutrin SR kind)

I was diagnosed with Optic Neuritis in my left eye, at the time of diagnosis, I felt fine. Had an MRI to check for lesions on the brain, there were none. I was put on IV solu-medrol for 3 days, then 90 mg of prednisone for one week, with a rapid taper the second week. 6 days into the prednisone, I started have shortness of breath, etc. Went to the ER and my white count was 22,000. Had bronchitis and the beginnings of pneumonia. Because of the breathing problems, I only did 2 days of taper (doctor's advice). I have lost site completely in the left eye and now I have blurred vision in my right eye. Extreme fatigue, and a mental fog I just can't explain. A "twitch" in my left left hand and muscle weakness. I just don't feel "right". How long does it take for this drug to leave your system? Has anyone had a similar experience? My eye doctor was considering another round of prednisone for the optic neuritis, but I am not so sure I can survive it.

I was given solu-medrol for an allergic reaction to something unknown. I was given benadryl just prior because of my itching hives.
Immediately after the RN injected the solu-medrol into my IV I started choking, I couldn't catch my breath, I felt as if I had a rush of adrenaline but at the same time it felt like my heart was fluttering. My blood pressure and my heart rate jumped up considerably. I was unable to speak and had a hard time swallowing. My vision was effected and I had light sensitivity, everything suddenly seemed very bright. My thought process was very distracted, I would try to speak and within a second forget what I wanted to say. I had to concentrate extremely hard just to get out a single word.
I also had slight numbness or loss of sensation in my hands.
I don't want to know what would have happened if I hadn't been given the benadryl first! I felt as if someone was inducing brain damage onto me and instantly turning me into a vegetable.

I have MS and FINALLY tried the Solu-Medrol. 3 days infusion and then once a month for the next 5 months. I have been on it for 3 months. The pain in my joints goes away almost completely, though it comes back sooner now than at first. It feels great not to hurt. The metallic taste and bloating is worth it. The first several years after being diagnosed, I would not take it. Now I can hardly wait for my next infusion. I also take Betaseron injections every other day.

I had solu medrol 1gm/200 ml infused for 3 days for new MS. First day I became pale and "dead" looking. I had weakness and confusion. Day 2 I was irritable and weaker. Day 3, I was even weaker and began having shortness of breath. Day 4, I woke up feeling like I was drowning. I shuffled as I walked, had a total of 10 pound gain, I was weak and unable to eat. I began to not urinating and had extreme abdominal distention. I could not go to the bathroom. I had to sit or sleep upright. I spent a lot of time sleeping. Day 5 sudden 6 pounds more gain. Had a feeling of death. Heart rate was high..checked in the hospital..BP 90/50. I was so weak that a whisper is all I could do. I spent 3 days in the hospital. Today out of the hospital, I can only eat same amounts. solu medrol caused my system to stop functioning.

Follow up to my post earlier today...

I took the my son to the doctor this morning and he was somewhat dismissive of the recent reports on Singulair...says he's had a lot of kids on the drug and never heard a peep about side effects until last week when the report on suicidal tendencies showed up. He did advise that when these kinds of behavior changes happen after a new drug is started he would recommend that we stop taking the drug no matter what it was, but I still felt uncomfortable with his response to us.

I felt like he was accusing me of making it up or only coming up with it because of recent news and message board posts. In fact, I made the appointment BEFORE I saw the posts. I was worried about his behavior BEFORE I saw the posts. It's just that seeing the stories from everyone else basically confirmed my suspicions that it might be the drug causing the problems.

I feel like I definitely wasted OVER AN HOUR waiting for a doctor to spend five minutes making me feel small.

Last night was the last time my son will take the drug, and I don't care what the doctors think of me.

Hello, my name is Rob and I have been on Remicade for the past 5 years. I had a reaction to my first Infusion, shortness of breath and feeling flushed. They then added Benadryl to all future infusions and everything has been fine until this last infusion in April of 2008. Halfway into the infusion my face became flushed, the person adminisitering the Remicade said it was hives, this was accompanied by tightness in the chest and headache. They stopped the infusion, gave me some Benadryl added to the IV, that did not work, they then added Solu-Medrol 125MG into the IV and it seemed to reduce the effects of my reaction. The infusion was completed and I went home. Upon arriving home I looked quite pale until that night. My face became red, almost as if I spent too much time in the sun and I have had a headache followed by chest pains. This condition has continued into the next day but it does not feel severe enough to go to Emergency. Should I be concerned or will this pass? Is it possible that I have been on it so long that I am now building up a tolerance to it?

my bf had an asthma attack and was given a iv injection of solumedrol at the emergency. when we got home he slept for 3 hours then got up in a bad mood. my daughters boyfriend started some arguing with him and my boyfriend was violent. we have lived together for 4 years and NEVER has he even raised his voice. he was irrational and very, very loud. this drug made him very angry and hyper. he said he felt like his adrenalin was through the roof. after work he came home and was calmer but his eyes were bothering him. (all day they bothered him) i will not let him take this injection again. this guy could drink a bottle of tequila and not be loud or violent. he is a very calm man. the hospital said he would have no side effects to really speak of. it took all i had to try to calm him. he also had 5 doses of albuterol inhalation and 3 doses of ipratroprium brom inhaled. could be combo of all, i don't know. but never again solu-medrol

I Have ms I just found out. They thought I had a brain tumor and the admitted me to the hospital and started treating me immediately with Prendisone.It has just been horrible do you hear me horrible!! after I weened off of them the moon face became horrible. I have knee pain and they swell. my legs and feet and stomach. I have swelling in my back that looks like a buffalo hump. It is horrible.please help me. I feel so unattractive I just cant help it. I am very grateful that it has helped me. I was numb on my entire right side that is another reason why they put me on it. I am glad that is gone, but I almost think I would rather deal with the numbness than I would all of this. It is really scary because nobody said anything to me about how it was going to effect me. Actually the nurses said that there were no side effects to worry about. well let me tell you it has been one roller coaster; i was pumped full of the Prednisone through an IV for thirteen days straight in the hospital,, then was sent home and was given the pill form. all together I have been on the Prednisone for 26 days straight. I will just be so grateful when all of this subsides.All I want for Christmas is to get this swelling off of me and get rid of the moon face and the joint pain. is that tooooo much to ask my goodness. I am so glad that I found this site. it has really been most helpful. I hope everyone out there has better luck with this than I have. it sounds like allot of people have problems. thanks

For optic neuritis, and arm and shoulder pain: I had a combo of 3 days of Solu-Medrol infusion (steroid via IV) and then went on the following regimen of Prednisone: 5 days 60 mg; 3 days 40 mg; 2 days 20 mg.
Side effects have been terrible with the WORSE CASE OF FACIAL ACNE I have ever had. I'm 28 - I have my 10th high school reunion, weddings, and more -- and it may sound vain, but if you saw this acne (hundreds of tiny pimples all over my cheeks; sides; chin; and upper neck) you'd feel my pain. Also, got shoulder, arm, back, and chest acne -- which I can take b/c I can find ways to cover that up. But face! It's terrible. I'm using Pro-Activ and see minimal improvement. The #2 problem has been SEVERE heartburn during the tapering off phase. I have never felt that much pain and it only went away after I completely went off the drug - I treated this with ginger drink (a hot tea sold in international food stores) and Pepcid AC. Also, due to my original symptoms I can do virtually no exercise when I used to exercise 6 days/week. I'm really worried about weight gain which I already see in my arms and face. My appetite has been through the roof. Irritability was the worst but I forewarned my family. My original symptoms have greatly improved, but I'd honestly rather fight through that original pain than endure the craziness that is prednisone.

I have been on pred for 6 days after takin solu medrol dose pack for 6 days for an allergic reaction. The med helped the rash and itch immediatly but as soon as i taper down the rash is back full force. I dont know what to do I cant take the steroids anymore, I am a rotten crabby person on these, i have heart palpitations and sever muscle spasms, it has to be from the steroids. If anyone knows how i can feel better please let me know. I also urinate constantly and only sleep in broke up cycles with wacky dreams..........

I've been taking prednisone for about a year, started with solu-medrol infusions of 1000mg for 3 days with a prednisone taper of 180mg a day for 7 and down from there, I have had 4 of these this year and now am taking 20mg a day, I've had many symptoms of taking so much pred, but it helps keep my vision normal and keeps the headaches away, weight gain, sleepless nights, now acne and just feeling bloated all the time are my main complaints, I am going to see another specialist to get me off prednisone, and will try another immunosupressant drug that dosent have near the side effects of pred, but all I can say is it works, but who knows what will happen to me down the road, I'm a 37 yr old male who feels like I've aged twice that.

I started on IV Solu-medrol this past Monday for an MS exacerbation. I was on it for five days. Yesterday was the fifth day.

I have had trouble sleeping, heart palpatations and today my face is very bloated and all flushed. The biggest thing I feel is that I am really out of it and feel really tired, but can't sleep. I hope these treatments are worth it and slow down the exacerbation. I went from 4 to 14 lesions in six months and have a new one on my brainstem. I am also on copaxone, so that could be causing the heart palpatations too.