Medrol symptoms and conditions

I was prescribed medrol by my GP due to an ongoing rash that needed to get under control. I believe I had the 40mg dose/wein pack. The first two days I felt as though I were on speed. Day 2 at the grocery store I stopped to take my blood pressure because I was sure my heart was racing out of my chest. Thankfully, it wasn't and happened to be palpitations that I was having. I had hot flashes where my face and chest would get red like a sunburn. There were the sweats and the leg weakness/soreness. I did have sporadic headaches but, nothing a Tylenol wouldn't alleviate thank goodness. I've read here that numerous people had very bad headaches. My last day on the meds I started to experience the fatigue. Today is my first full day off and I certainly felt flu like. Sporadic lightheadedness, weakness and fatigue that would all come and go throughout my workday along with sporadic energy. I'm glad that I found this site so at least I know that this is normal and will subside in a few days. Other side effects I experienced were worsening of my post nasal drip along with a funny taste in my mouth, mood swings, insomnia, hyperactivity and muscle aches.

I received an injection from my doctor of what I thought was depo-medrol.
He gave me this injection in my upper arm. I now have an indentation in my arm.(I can put my finger in it.). The next time I got a shot, his nurse gave it to me and, again, I thought it was depo-medrol. I showed her the area from my last shot. She said "oh, a shot can't do that". Then, she gave me the injection in the same arm. (different spot). It was so quick, I did not have time to say not in the arm. This time it felt like someone pouring acid on my arm. I have never felt anything like it! I told her that it hurt. It was getting more painful, by th time I reached check-out. I was feeling overwhelmingly sick, and lots of pain. I asked for the doctor. He showed me the bottle that was given (dexamethasone) He said it was the same medicine that he had given me last shot. I showed him the indentation. He thought I was just having a reaction of anxiety from getting a shot.
This indentation in my arm seems to be growing. Now it is in an "L" shape and skin is red. I thought I heard him tell the girl at the desk that he gave me a shot of Kenalog, but he showed me the other bottle? I don't believe that these are the same medicine, but it sounds like the same symptoms.
My previous doctor's nurse used to give me the steroid shots in my buttocks. I never had any problems with them. If someone knows how to deal with this issue. let me know. I just want the spot to stop growing, and it is painful.

My Mom was prescribed Levofloxacin ( AKA Levaquin) by her retarded doc for a mild cold and a sore throat.
After taking 2 tablets of 500mg each my mom is down is severe pain all over her body! she has joint pains, neck pain, arms, palms shes got severe pain all over her body!
She also has severe itching on the palms and her arms as well..
Headaches,
Things aren't looking good.

She in real pain! She tells me she just wants the pain to stop and that she was better off with the cold and sore throat.

She has stopped taking Levaquin.

Anyone got anyway to help her? something?? She is asleep now but tmr Im going to ask her to drink some kefir..

Thanks

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)

On less than a week of Medrol Dosepak 4mg, swollen glands under jaw/chin area, neck, back and sides pain (fluid retention). Did not finish dose pac (left 3 or 4 tabs without taking). Increased appetite!!!, weight gain of 6-7 lbs! (in less than a week), dull headaches, increasing to a migraine even after not taking them for 3-5 days! Depression, tears flow out for no apparent reason at all. If any natural alternative med did a quarter of what this one does, the FDA would be shutting them down gestapo style in no time.

I am new to Topamax. Just started for severe/horrific migraine pain - I have been getting migraines that lasted 8 days long without relief for the past few years, popping imitrex like m & m's. Mine seem to be related to a drop in barometric pressure as well as to being perimenopausal. They were ruining my life. I am currently on the 25 mg in the am dose and 50 mg pm dose schedule to titrate up to 50 mg twice daily. So far I have had only 2 migraines in the past 30 days instead of 8-16!!! I am a much happier person- I can't even describe it. People at work even tell me I LOOK different! I do however, have some intermittent tingling/numbness in my fingers mostly, passes quickly, little back pain, and some little headaches that come and go. I can so deal with these. I have only had to take Tylenol or Motrin on three occasions in the past month. I used to take two imitrex and still had take 400mg of Motrin and 1000 mg of Tylenol just to numb my migraines. Can I tell you I used to be somewhat non-functional and still go to work everyday- I am a nurse!
So far Topamax has given me my life back because I seriously considered driving into a tree one day on my way to work before starting it. Wish me luck.

I have been taking Bupropion XL 150mg ("generic" Wellbutrin) once a day as a mood stabilizer everyday for exactly 2 weeks. I suddenly developed severe itching in random different areas on my body. My lower scalp, palms of my hands, and ankles were the first areas that itched but did not have any obvious marks on the skin as to what was causing it. About 3 hours later it became progressively worse and started showing tiny red raised areas in the previously stated places on my body and started to spread to my neck, wrists, mid-chest below my breasts, behind my knees, and upper thighs near the front panty lines, but even worse on my lower back.

I was becoming a bit scared and annoyed by the constant itching and the hives that were forming in those areas. I had never in my life had hives before. The bottoms of my feet were so itchy but they did not have any hives on them, they just itched! I took 2 benadryl and tried to sleep but woke up quite a bit during the night because of itching.

By morning, the hives were worse and especially on the back of my neck where it was swollen and red and I could not even bend my head back. My face was slightly swollen and my eyes were puffy as well. My right palm was so swollen and painful and I could not make a fist.

I called my doctor but he was on vacation, so I had to talk to a message service he had set up in his absence!
I went to the emergency walk-in care center near my home and was evaluated by a physician who concluded that all this was actually due to the Wellbutrin which I myself found hard to believe and wanted to deny it in my mind. He ordered me to stop taking it and prescribed all sorts of drugs to counteract the hives and itching.

I am writing this only about 9 hours after seeing the emergency physician and have had some rest and taken my prescribed medicines, Medrol ( a steroid-type drug) to treat the swelling, Hydroxyz hcl for the itching, Allegra for allergy, and Zantac for the side effects (stomach pain) of all these drugs I now have to take for a while!
The swelling has gone down a bit and itching has subsided somewhat. In conclusion I must note, that it was the pharmacy's decision to substitute the Wellbutrin my doctor had prescribed with a "generic" version (bupropion) that is still so new to the market and is still undergoing studies on human subjects. We are the guinea pigs and did not even know it.

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.

Hello everyone, I just started taking Prednisone today for severe Sciatica. I have read all your stories and now im so weary of taking another pill. Some of the side effects that y'all have experienced are awful. I think i would go crazy if i got all of that. I am on the Medrol Dose Pack and i started 2 pills before breakfast and now i have some stomach pains. Its sad that you have to take this for pain and inflammation and then end up with all other kinds of problems. Thanks for sharing your stories. I think im gonna stop taking it all together. Stacey

As a Doctor myself I think drugs are NEVER the answer except in EMERGENT issues in Heroic life saving... YOU however and all individuals are and should be MORE accountable for your own health and STOP DEMANDING the Drugs and look to LIFESTYLE changes in DIET and EXERCISE to achieve the GOALS so necessary for quality and quantity of life.... The tools are at your fingertips ... The almighty internet ... And your OWN imaginative mentation is your TRUE limitation... So TAKE control of yourself and BE accountable .... Sorry so blunt but MORE tough love and Educating people is whats needed.... NOT more drugs....

MDG

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.

HELLO EVERYONE....IM SITTING AT WORK AND JUST DECIDED TO RESEARCH THIS DRUG LISINOPRIL...BECAUSE I AM REALLY BORED....WHEN I GOOGLED THE NAME I CAME ACROSS THIS SITE.....OMYGOSH...I THOUGHT I WAS GOING CRAZY...I HAVE BEEN TAKING Lisinopril FOR ABOUT 6 MONTHS NOW....I ALWAYS READ THE INSERTS THAT COME WITH THE MEDICATION BUT I NEVER SEEN THE SIDE EFFECTS THAT WE ARE HAVING ON THE INSERT...I SING IN THE CHURCH CHOIR AN I ALWAYS WONDERED WHY MY VOICE WOULD BE SO HORRIBLE AND MESSED UP..I AM SO HAPPY I GOOGLED THIS DRUG...DOSE ANYONE KNOW HOW LONG IT TAKES BEFORE YOUR BODY GOES BACK TO NORMAL AFTER STOPPING THE DRUG....

I'm a physician. Usually Kenalog injections can be avoided and oral steroids used like prednisone. The local dimpling effect may occur if the injection is too shallow, actually there is a temporary "disolving" of the subcutaneous tissue, the muscle and joints are not damaged. It is usually viewed as a "cosmetic" adverse effect. The Kenalog injections was primarily designed for joint injection and the kenalog or similar depo form stays active in the joint for a few weeks. All steroid medications can cause irritability and this is usually temporary for a few days. Steroids can cause muscle weakness- this is usually associated with high doses for prolonged use like being on prednisone for 3 or 4 months. Steroids can have an adverse effect on menstruation, but this is usually associated with chronic use. The most serious problems with the steroids result in bone weakness(osteoporosis) and serious damage to joints like the back and hip. Steroids can also result in weight gain, diabetes, high blood pressure and cataract formation. I don't think Kenalog is any different than other steroids such as Medrol or Prednisone in terms of the side effect profile. These are dangerous medications that can also be very helpful in saving lives and diminishing pain.

I was prescribed a 6 day pack of 4mg Methylprednisolone (Medrol) at the ER for an allergic reaction I was having to a gel that I used on my sking. The Medrol worked great at stopping the allergic reaction. My swelling, pain, and rash began to rapidly clear up. Unfortunately I began to have many side effects. On day 5 I was unable to get out of bed I was so tired and dizzy. I had a headache and mental confusion and unclear thinking. I called my primary care provider on a Sunday to ask if it is okay to stop taking the steroid. She said it was and that it was unlikely the medrol was causing my symptoms. She told me I had a virus. I told her the symptoms I was having were listed as side effects on the drug info sheet but she did not believe me. IA few days later I made an appointment to see a doctor, not the same one who took my phone call. This doctor said all of my symptoms were from the Medrol. She knew because of personal experience she saw in her mother who was also taking steroids. She told me medrol can cause a manic response or a depressive, the latter is what I was having. As part of my exam she wanted me to have blood work but said I should wait at least 2 weeks to allow the drug to get out of my system. It is now 19 days since my appointment and I am still having side effects: nausea, complete lack of appetite, dizzy, and tired all the time. I put a call in to my doctor today and am waiting to hear back. I am sorry that I took this medication, will never take again. How long will it take for this med to get completely out of my system so that I feel normal again?
A friend told me her mother had a manic episode on steroids. When I was younger I took steroids for a brief period and had much milder side effects.

Hello all,
I'm in the same boat but near the end.... I was given Bactrim for a UTI. I woke up after 2 days with horrible aches in my joints and muscles. I was immediately taken off the Bactrim and put on Doxycycline. I was then put on Prednisone for the aches (which helped). I developed blisters and a rash after a few days. My aches went away after about two weeks but now I have itchy, sore and peeling feet, buttocks, mouth, and genitals. Stomach upset as well. I have been tested for everything (STDs, Lyme Disease, West Nile, etc, etc) and everything has come back negative. I was diagnosed with Stevens-Johnson Syndrome from the allergic reaction I had to the Bactrim. It has been 3 weeks since the first dose and I am finally starting to feel better (except for the insane itching). Good luck to everyone. Never again!

I've been getting Depo-Medrol injections in my back for years for degenerative disk disease, and many other things with my back. I recently moved to an area where they have given me 180 mg of DepoMedrol in my neck, thoracic and lumbar spine. I have gained 30 pounds. I am a tiny person and this weight gain is affecting the way I live my life. I've been trying and trying to loose it and it just won't come off. Can anyone help me?

My jaw dropped after reading all of these posts. I started on Yasmin 3 weeks ago. I've never really been on BC's before, so I thought that my headaches, numbness and fatigue were just because of school. I finally connected the dots and looked on the internet to see if it was the Yasmin or if i was just crazy. I am so thankful to have found this website. I wish it was in the paper or advertised. Doctors should not even be able to prescribe this drug.

I just finished my seventh day of Avelox today for rhinitis (sinus). The dry mouth and throat is very bad. I wake up about twice a night to drink water. My mouth and throat gets so dry. It even gets dry and sticky throughout the day. I am drinking so much water. I have noticed about an hour after I take it, I get dizzy and become very anxious. I even start thinking about all of my symptoms and begin to freak out. I have had about two panic attacks this week. I do not like the changes it has done to me. I have also been very emotional and sad. I think I have cried about three times this week. I am glad I am finished...no more depression! My sinus infection is better though.

Prescribed 500mg of Levaquin for sinus infection, along w Medrol Pak steroids. Although steroids can cause restlessness, they do NOT cause COMPLETE anxiety, nightmares insomnia and aphasia. I took only 4 pills, 1 each day, and it's like i boarded THE CRAZY TRAIN. Fluoroquinolones are apparently known for their intense and dangerous side effects, and if it is true that this is also an antidote for anthrax poisoning, it's probably something that should not be prescribed for sinus infections. SEVERE side effects, chest tightness, etc. No wonder they will not rx it for teenagers-I am a healthy 42 yr old woman and would NEVER take it AGAIN,.

I had been taking bactrim for a week when one morning i woke up feeling achy, tired, and light-headed. I noticed a slight rash forming on my arms but didn't think much of it bc i had been on the Bactrim for a week already. Then the symptoms got wayyyyy worse. I started to form lesion like sores on my vagina, and I immediately saw a doctor to get tested for STD's. The gyno examined the area, and she said it did not look like herpes but that she would test for it just in case. She put me on augmentin bc she said I definitely had some sort of infection down there. After taking 4 doses of augmentin almost all the lesions went away. The STD tests (blood, culture, and urine) all came up negative, as I expected they would. Has anyone else had genital reactions to bactrim???? Because as of right now the doctors are unsure what caused this outbreak/infection.

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?

i had this shot last June. i would never do it again. i had insomnia and night sweats for a month. i was up every hour on the hour wiping my self dry i was dripping wet from head to toe.. i had to wear my husbands running clothes for the sweat. the sweat was making me cold with my pj's. had to sleep w/ towels.every morning i would be so depressed from not sleeping i couldn't function at work. had severe anxiety( had to go on Xanax) had hair thinning, I lost 6 lbs went down to 100lbs and I'm 5 ft. become severely anemic the doctor wanted to do a blood transfusion. i could not stop bleeding for months clots galore. this is just a short version of the problems. the drug finally stopped working after 9 months.doctor wants to give me depo medrol. i don't think so!