Prednisone symptoms and conditions

I am 50, pretty healthy, but have had a new condition of inflamed and severely painful joints and muscles limiting activity. Doc put me on 60 mg prednisone for 3 days, then 40 mg 3 days and 20 mg 3 days. First day was ok. Since then I have been a raving lunatic! I read the post about the person chasing their cat around and had to laugh and relate. I flipped off the neighbors workers because they were backing up a truck and it was noisy! It is all I can do to keep myself in check. I have canceled/rescheduled all unnecessary appointments until next week when I am finished. I "sleep" about 3 hours a night. Last night I peed the bed. I eat constantly. I have to work and concentrate (teach college) and that is so hard. I imagine my students must think I am on meth. I can't take it any more. I have 1 day left and I am not going to take the last one. I hope that this regimen will have calmed down the inflammation and if it recurs I will seek alternatives. AM NEVER going back to prednisone unless it is life or death situation.
Good luck to all those out there who have to take it long-term. Bless your hearts.

Hello I am 40 yrs old and got a lung infection which cause swelling in my lungs so the put me on high doses of prednisone via IV for 21 days in the hospital. The drug saved my life and took it at the same time.

After I got out of hospital i was on 60 mg for 6 weeks the 30mg for 6 weeks then 20mg the 10mg. It has been a living HELL over the last 5 months or so.

I told my DR. i have very bad blurred vision and he said it because the med runs my sugar up but I check my sugar and limit my sugar and it around 100 all the time which is normal soits not sugar. Then he said well them you need to see an eye dr. cuz your eyes are going bad. I begged to differ with him and told him if there was something wrong w my eyes then why is is one day I see fine and the next day all blurred and then back to normal!? it this stupid steroid if you ask me plus on day my right eye is bad and next day my left uggh!

The WORST side effect it the brain fog as yall call it. OMG I feel like im loosing my mind and going crazy. The dr. says hes never heard of such with a wise remark and says you know where your at now right? I know where i am and what I say but I feel like its not really happening. Its like im dreaming it. I feel like Im trapped in my head and I lookout blurry eyes.

Before I was a very confident independent person but now I feel scared all the time i feel hopeless and ive went through 3 girl friends over the summer because of the extreme forward attitude the med gives me. I am not the same person I was. I some time just want to die. I'm extremely tire if i do any exercise at all.

Plus I have all the other typical side effect like the moon face and weight gain. I don't even look the same cuz my eyes have huge bags under them and a double chin I never had.

I feel for all of you because i know what your going through.
I saw one comforting post in here where someone said within 2 weeks of completely getting off the pred. he was his normal self.
I CAN TELL YOU HOW GLAD I WAS TO READ THAT!

Please if you have finished the med and have got back to normal don't forget about this post. Please let us know because we need any hope we can get to keep our chins up and not loose hope and go completely crazy or worse kill ourselves.

I have about 4 more months of this LIVING HELL and I will surely let you all know if it get better. If you have come off of it and are reading this PLEASE let us know if we get back normal at least w the brain fog. I can take all the side effect ok except for the crazy dream zone zombie feeling.

I WOULDN'T WISH THIS KINDA HELL ON THE DEVIL HIM SELF!!
Let's pray for each other that the Lord keep out minds strong until we get off the nightmare drug call Prednisone.

side effects:
brain fog, blurred vision, puffy eyes, depression, confusion, dizzy, moon face, buffalo neck hump neck, hopelessness

I started taking this on October 8 for a sinus infection. by the 13th I was suffering intense headaches, nausea, fever of 102 and anxiousness. I thought that on top of my original ailment I also had the flu. After 2 doctors and a trip to the hospital in which no one thought of the side effects of this drug, and with the discovery of a full body rash 2 days ago, I finally called my pharmacist yesterday who told me to drop the drug. I then looked up everything I could find myself and this is obviously the result that so many people describe. I am now on benadryl and prednisone and still quite miserable. I think they should take this off the market since so many people have a bad reaction!!!!!!!!!!!

hair loss, neuropathy in my right leg, complete exhaustion, numbness and tingling, stabbing pain in my back that wraps around my chest, headaches, depression, paranoia, stomach pains, chest pains, tremors in my head, pain down my neck, pain in toes, blurred vision, tearing pains in feet, very weak, moody, pain in face, really bad symptoms week prior to period, cracking sound in joints, -- Have had symptoms for three years and just had a neurologist confirm today that all of these problems have been caused by my doctor prescribing avelox and prednisone!

Was prescribed avelox for bronchitis. Took it for the full ten days. began having diarrhea. It has been 5 weeks since i stopped taking the medication and have continued to have diarrhea, cramping, abdominal pain. The diarrhea is a loose stool. Have had stool tests done and do not have a secondary infection from this.

i went 2 the specialist yesterday that put me on the prednisone due 2 me having crohns as the joint pain in my ankle has been so painful and his now told me that the prednisone has giving me arthritis im really upset about it im 25 and im in a lot of pain the specialist said 2 go home and rest my ankle for the weekend its been 2days and its still not better iv got 2 go back and see him on Monday and if it hasn't improved which i doubt it will his going 2 change my medication he wanted 2 up the dosage of prednisone to 30mg as im down to 10mgs now and i told him that i have received every side effect possible 2 the prednisone and its just starting to reverse and there is no way im going to le you put me on a higher dosage i want 2 come off this drug as quick as possible and he surgesseted another medication that will help with the arthritis in my ankle but it will make me nausea i told him id rather that then all the symptoms iv been having in the last month then be put back on the prednisone

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.

iv been diagnosed with crohns 2months ago iv now been on prednisone for 4weeks i started on 40mg and now down 2 15 the last week my ankles have swelled up and now my right ankle is so painful to touch and walk on, and nothing is making it better, pain killers don't work, massaging it doesn't work, putting deep heat on it so to night i iced it for 15 mins and put a heat pack on it several times the pain went away for 10mins and came back its so painful im almost in tears, im down 2 15mg now so im not eating as muchas i was b4 i wasn't getting full i just keeped eating, my mood swings arnt as bad iv got moon face as they call it and i hate it as theirs no shape at all 2 my face, im getting pimples as will iv retained all this fluid and i feel like a marshmallow can someone please tell me that this pain will go away or is their something i can take 2 make it go away this is the worst medication in the whole world when i get off the prednisone and i have another flar up id rather have the runs and stomach cramps then all this drama iv been having in the last 3weeks iv also changes my whole diet and its made a huge difference 2 how i feel

i was put on prednisone 3 days ago due to asthmatic bronchitis. i was put on 60 milligrams a day. which to my understanding is a really high dosage.
long story short my cat would not stop meowning and it made me so darn angry that i wanted to throw him around the room and kept chasing him around screaming at him to shut the bleep up and tearing him out of the window every time he tried to get up in the window. i love my cat dearly and he is like my child. i have never EVER treated him badly. he gets more love and affection than most people give their children. he was crying and scared to the point of defecating all over my room. this had no affect on me. it just made me more angry. normally when an animal is scared or hurt i am incredibly empathetic.
on top of it i have had severe nose bleeds, and severe heart palpitations. this is after only being on it for three days.
i know this product is good for its purpose but as far as the side effects go, i think i would just rather live with my asthma symptoms. i was scared that i was going to lose control and injure myself or my cat or anyone who got in my way. i do not recommend this drug by any means.

within about one or so hours after having been injected for a Ct Scan I began to shake uncontrollably and feel very ill and also had severe pain in my coccyx. I had to be admitted to hospital where I was treated with an IV drip containing about 100 mg of prednisone.My creatinine level increased above the normal limits but reverted to normal after about 2 days.I was very listless for about 3 days.

I have been taking prednisone for three years now and I love it. When I am off of it I cannot breath and I get fluid in my lungs and my arthritis comes back and I ache all over. I could not live without it. The only side effects I have is a little weight gain, sweating, and moon face but the side effects are better than the all over acheing and not being able to breath. This drug has been very good to me.

I am so relieved to have found this site... i have been miserable for almost 2 weeks, i broke out with hives last week and never found the cause but with that and some breathing problems they put me on prednisone. I have been miserable since, i couldn't eat drink sleep or do anything else at all pretty much and i have had diarrhea, and a ton of other symptoms... i feel bloated acid reflex muscle aches headaches dizziness chest pain & pressure very weak feeling mood swings and depression the jitters and heart racing and from what i read and researched this is all from the steroid prednisone.... thankfully the doctor ended my dosage sooner than it was prescribed and last night i took my last pill... i now am just wondering when or how long will it be till i feel myself again and can have a good nights rest?? I will never use this medicine again!! I am just soo relieved to have found some answers on here.

I had a bulging disk and a pinched nerve and was put on PREDNISONE - 60mg for 5 days, then 40 mg for 5 days and then 20 for 5 days. I had a round face to begin with, which I always hated, but now, my face just looks like a balloon that someone painted a face onto. I have a huge face, a double chin, huge stomach, I look 5 months pregnant and I absolutely HATE myself on this drug. I've been off now for a week and nothing has subsided except the sweats -- very embarrassing! I work and in the middle of a meeting, I sweat so badly that it rolls off my giant red face in rivulets. I'm just miserable. Does anyone know how long it takes to get rid of the side effects of this demon-drug?? I want to stay in the house and hide.

Hello,
How long do side effects last after completing steroid treatment? I've been off of pred for 4 months for crohn's first time. I was on 40/30/20/10 for a 6 week period. When I got to 30 my legs went into extreme pain. They felt like they were on fire, burning knees. Went to several doctors. One said steroid withdrawal, one said inflammation of nerves from Crohn's. Neurologist put me on neurontin to get off of the pain meds. I am still in excruciating pain and wondering if it really is steroid withdrawal. I can barely walk at times with extreme sharp pains, like someone is stabbing me in the legs. Can't stand for long periods of time and pain pills barely touch the pain. During steroid treatment, they gave me 3 rounds of Dilaudid in the ER and I was still crying, and I don't cry. Has anybody ever had this effect this long after being off the drug??

My husband was prescribed 80MG of Prednisone a day because he had cerebellitis. Yes, they saved his life so for that I'm happy, but now he is out of the hospital and I have little to no patience with him. He is crying all the time. Everything I say or do makes him cry (and he's never been the crying type). He is needier than he's ever been before and I go to school full time and work full time so I have very little time to spare. It is very difficult to have all my home time taken up by everything he is afraid of----because that is all he can think about. In fact when he can't cry or talk to me about his fears (about not getting better) he obsesses about them keeping him from sleeping. We are finally able so go off the the medicine so I'm hoping that his anxiety will go away with the meds!

I used prednisone for sinus inflammation and it gave me bad side effects such as: irregular heartbeat and stomach upset and anxiety. It actually did help with the inflammation but I stopped using it because of the side effects. It made my lip puff out too, which i did not mind because i have small lips and i looked better with a bigger lip, lol! I am thin so if it made me swollen i did not care because i need to gain weight, i am only 105 lbs. I just started taking methylprednisolone tablets packet and they seem to work better and if it causes increased appetite that would be good for me because i lost so much weight because of my teeth and sinus pain i had everyday for four months. So far it is working but i just started it and will keep you posted. It does seem milder than plain prednisone I suggest you switch to this if the prednisone is not working for you. It sounds like most people are on too high of a dosage and take with food and a lot of water. Hope everyone feels better soon.

SINGULAIR'S LABEL HAS BEEN UPDATED:

The following has been added to the "Precautions" section of Singulair's label:

"Neuropsychiatric Events
Neuropsychiatric events have been reported in adult, adolescent, and pediatric patients taking SINGULAIR. Post-marketing reports with SINGULAIR use include agitation, aggressive behavior or hostility, anxiousness, depression, dream abnormalities, hallucinations, insomnia, irritability, restlessness, somnambulism, suicidal thinking and behavior (including suicide), and tremor. The clinical details of some post-marketing reports involving SINGULAIR appear consistent with a drug-induced effect.

Patients and prescribes should be alert for neuropsychiatric events. Patients should be instructed to notify their prescribe if these changes occur. Prescribes should carefully evaluate the risks and benefits of continuing treatment with SINGULAIR if such events occur (see ADVERSE REACTIONS, Post- Marketing Experience)."

I used the Neutrogena 30 sunblock for the face with self tanner this past weekend with Helioplex. Unfortunately it was the only sunscreen we had on the boat, so I also used the sunscreen on my back, arms, neck, and knees. I broke out in a rash/hives within 24 hours of using it in all the areas that I applied the sunscreen. I am on a full week course of prednisone because Benadryl alone was not helping.

I do have sensitive skin and was excited about a sunblock & sun tanner combo. I thought I was being healthy--take one look at my face and it doesn't appear so this week!

My husband was given Levaquin and Prednisone in April for a bad chest infection. The last day of Levaquin, his knees began burning. He has been suffering with pain and cramps from his toes all the way up his legs. It has been in his fingers up through his elbows. He has shaking in his hands. He had an abnormal EMG. He has intermittent low grade fever. He started having trouble swallowing a couple of weeks ago. He now has to go to speech therapy because his tongue muscles aren't working correctly. He had none of this UNTIL he took this medication. The doctor now finally feels it is as a result of taking the Levaquin. The prescribing doctor had the nerve to lecture us about NOT stating he was allergic to the medication because he would be in the hospital with an infection otherwise. We are not returning to this doctor.

My 62 year old husband has had Parkinson's for about 10 years now. The other day he was prescribed Prednisone (20 mg tablets, twice a day) for 5 days. After the first day his pinched nerve problem was greatly improved, and as a side effect, his Parkinson's symptoms disappeared completely and he was like normal again! This is a miracle to us and we are looking for medical research to help prescribe Prednisone for Parkinson's', or some agent similar. Did the Prednisone make the other Parkinson's drugs more effective; or did the Prednisone fix the Parkinson's on its own. We don't know. For 5 days, it was bliss; I hope we can get someone to weigh the side effects against the miracle of being normal without any Parkinson's symptoms!

I have no idea if these are side effects from Remicade or not- because doctors always dismiss it as "probably just you". Definitely HEADACHES. I would occasionally get headaches before, but since being on Remicade the past year, I get really bad headaches. Neck/scapula pain/strain. I have woken up with immobile neck 3 times now in past 2 months. It's getting ridiculous. The doctors just say I need PT or to stretch. But I really wonder what's up and why I've never had that in my life until now. Also flushing with inital infusion, but that really is no biggie. I definitely feel STUPID. I've heard of "chemo brain"- does the same thing happen with Remicade?
I am 31 and taking this for inflammatory condition NOS. I have an autoimmune/inflammatory eye condition NOS that left me with significant Retinopathy. I did Prednisone, Methotrexate, Humira, Cyclosporine, Tacrolimus, Cellcept all for a few years- and nothing helped except steroids. Which obviously you shouldn't take long-term. Plus I HATE them, they make me fat, hairy and psycho! So Remicade has been a god-send in some ways. But I am a mother of 2 and love my husband, and worry that I may not go blind but will die young from side effects of this medicine. But why should I worry? Every health care professional says there are "NO" side effects. What's the deal?

I am 18 years old. I started yaz three months ago. During my first month taking yaz, i had a really bad fever and started getting these electric shock sensations in my head. My heart was racing and I couldn't stop twitching. I was panicking and will skip the long er story but the doctor told me it was anxiety and an allergic reaction to my cough medicine and sent me home with vicodin and atavan. I got better and didn't have that sensation for the next week. However, I was growing increasingly anxious and panicky for no reason at all and would have long crying jags where I couldn't calm myself down. I am usually a very happy person, and I just feel so depressed. The shocks started coming again, along with the twitching and feelings of vertigo. I started thinking that maybe it could be the yaz causing it and went off it mid pack. I went to my doctor for the shocks and she had no clue. I had a mri of my brain and it came back normal. I have been off yaz for two weeks now, and have since seen a neurologist. She put me on an 80mg prednisone pack which she said would stop the shocks but only have me the worst migraine of my life and shaking so bad that I couldn't function or leave my bed for for four days. I went to a new neuro and am on an new migraine medication which seems to be working better as I am up and my headache is better. He seems to think the shocks are a result of yaz. Have any of you had this symptom, and the twitching? I feel like someone has turned an electricity switch in my body and I cant stop moving. I have no clue whats wrong with me and its really scary. The only way I can sleep at night is with ambien, and I cant stop twitching even during the day. If yaz can cause this why can they even sell this awful pill?

37 - Dx'd w/ Hyperthyroidism at 20 and have been on levoxyl since then. I started at .075 and was increased to .1 when I got pregnant w/ my 1st child at 29. I always thought I had anxiety so until I started reading the posts I didn't put it together. I was always shaky and nervous and super skinny before I was dx'd with hyper and after the treatment I was still anxious so I thought it was a different problem.

The anxiety has gotten much worse in the last few years w/ pressure, family, and career so I went to a psych last week and he gave me lexapro and klonopin. The klonopin had done nothing and I was treated 10 years ago with Zoloft which made things MUCH worse so I won't take the lexapro.

I recently switched to Synthroid .1 because I thought maybe the generic meds didn't work as well. I developed a small rash on my elbow a week or 2 later, then a week after that I got 2 big patches on my back over my kidneys. A bout 2 weeks later I developed a HORRIBLE itchy rash over my whole body. I thought the itching would drive me insane. I saw a dr who gave me prednisone (made me feel awful), after I took the dose pack it came back like crazy. I went to the ED and the dr gave me scabies medication (I was mortified) but nobody else in the house had anything. I went to the derm and they biopsied two areas and a week later have not given me the result. Meanwhile, I'm back on levoxyl and the rash is slowly getting better. It must have been the cause. Anybody else get that??

Warning: I do not know if this is related at all (or if there is anyway to know for sure). I accidentally saw a connection looking up conspiracy theories, and I can't seem to find any "real" information about it at all.

My daughter at 14 years of age had this shot. She didn't feel good after, but I thought "normal" vaccination reaction and haven't thought about it since. Feeling a bit faint, a fever, and such.

However, last September (a few months later) she was diagnosed with autoimmune hemolytic anemia. It started with her heart racing, she looked pale (and sometimes even yellowish), tired all the time, her urine turned a dark color, and fainting. Not knowing anything about this I assumed that she was dehydrated, and had her drink lots of water. Until she started fainting, at which time I took her straight to our family doctor. (Another reason that I wasn't to worried is she actually had been to many doctors who didn't seem to think this was abnormal.)

She started on high doses of prednisone to keep her immune system depressed, and has now moved on to mercaptopurine (as the steroids made her suicidal.)

I plan on bringing this "possible" connection up to her hematologist and I will report back (she has an appointment on the 11th.). However, I think it is better to do a little scare here, and possibly help someone rather than take for granted that I am not sure... (So take this information with a grain of salt.)

Also note that this was sudden onset, they can find no cause, and we have no family history nor any of the other typical reasons (sometimes can be "medicine" induced.) 10 months later she is still testing positive on her combs test though.

I've been on Prednisone for about a month now and have experienced the racing heart. I've been thru so much lately and hope we can help each other here....for the asthma and other reactive friends - try an ALCAT test. This will tell you what foods/meds you have an intolerance to. They send you a kit and you may be surprised what happens to your body when you consume something that your body doesn't like. They have also just given me a script for Methotrexate because my RA numbers are high...I've done my research and so far am refusing to consume that toxic drug. Has anyone tried Minocycline (or other drugs in the cycline family) for joint pain, RA??? I hear it works and at least those side effects aren't deadly.