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PredniSONE and severe pain

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50 Side Effects posted for PredniSONE

September 15th
2008
12:29 PM

I took prednisone for 6 days ( the pack). Six the first day and five the next till day six I had one pill left. I have never experienced hair loss like this. I have a patch of hair that fell out in a circle the size of a 50 cent piece. I didn't notice it really falling out but noticed a bald spot and I freak out. I came on line to get info about this medication. This drug was ordered for me because I have severe pain in my back due to osteoarthritis, sciatica and back surgery. I was told taking this would help with the inflammation and might relieve some of the pain symptoms. Well, I think the pain would be better then the side effects that I suffer. I had loss of appetite and acne on my face. I feel dizzy and bloated. I pee all the time and seems like i visit the bathroom much more often for other reasons too. I have felt like a crazy lady and have less patience than normal. I hope that this does not last for ever. This is a small amount of the medication. I am sorry for those of you that have experienced a long period of time on this medication. I pray for you that they will find another alternative with less effects to your bodys.

-- By teralee65 | Reply | (3) replies | Private Message me

April 14th
2008
2:59 AM

I was put on Prednisonsone for Uveitis, inflammation of the eye. He started me on 20mg at 9 pills a day, then each week it was lowered to 6 pills then now i'm on 3 pills and then next week it will be 1 1/2 pill and i'll be off. I got the puffy face, my feet swelled, everytime i hate my stomach bloated and hurt, my face and neck turns red, i stayed hungry although i fought the temptation of eating for not wanting to gain a lot of weight, which I don't think I've gained any. But now I wake up in the middle of the night and severe knee pain, it feels like my knees they are in some kind of device that is crushing my bones they hurt so bad. i caught a bad cough and it's been around now for about 2 weeks and won't go away, i told the nurse about it and she says, i probably just got what everyone else has gotten, just a bad cough, well what's if it's some kind of infection? I look like a chipmunk, my face is so puffy. When i get off these prednisone in another week I WON'T BE going back on them, no matter what the case. I'm in more pain being on them and have more side effects while on them than the problem i was having with uveitis. I think some co workers thank I'm over reacting, but they're not here they don't see all the pain and frustration i'm going through while on this drug. The leg pain just started this weekend and i Know i can't deal with waking up everynight like this in severe pain. Everyone just makes me feel like i'm over reactin and it's nice to know that somebody out there is going through the same thing. Any comments will be great.

-- By tonyas | Reply | (9) replies | Private Message me

February 27th
2008
11:56 PM

Hi! I was diagnosed with wegener's in Dec. 2007. I was hospitalized for 6 days. When I left the hospital I was taking 80mgs of pred's. After 8 weeks I am now down to 60mgs.{per day} I found it amazing how the doctors didn't inform me on the very well on the side effects of pred's. Plus bactrim,actonel,protonix,vitamin-d and cytoxin chemo once a month for six months or more.{i have had 2 four hour infusions,getting ready for my 3rd one in a few days}.
I have severe moon face,buffalo hump. My neck and throat feel full. Almost as if I was drowning.I've gained 25 lbs.,I have severe pain in my legs and knees,my back between my shoulder blades from the massive hump that I have,which by the way makes it hard to sleep. I am puffy all over,I feel like a huge sponge in the ocean!!!!! I only hope that when the med's are over I will return to normal. I cry a lot because of all the changes to my body! I don't feel like getting out, afraid people are laughing at me, my clothes look horrible,and my memory has been fading! I sometimes feel like I'm in the "o" zone.
I am grateful for the wonderful care my doctors have given me,I just wish that they would of prepared me a little better for what I was facing for possibly a year!
For every one out there that are facing all types of effects,just remember not to forget who you are and things will get better.

-- By debbiewhite9221 | Reply | (2) replies | Private Message me

November 1th
2007
8:38 AM

I've been on Prednisone after and allergic reaction to penicillin (Amoxicillin) (bullous pemphigold - large blister on my arms and legs, some on the back and very little on the stomach) I've been on the medication for three days (40mg/day) I cannot standup or move my hands, my entire leg hurts and the foot is swollen (it could be from the penicillin). I'm hoping it will go away after I come off prednisone but has anyone experienced long term pain from this drug?

I'm pretty sure my pain is from the allergic reaction. Has anyone had long term pain from any type of bullous reaction?

-- By speedysa | Reply | (4) replies | Private Message me

November 8th
2005
1:35 AM

Six weeks ago, I took prednisone for ten days for joint pain and swelling (both hands, both knees, both feet etc. ). the swelling subsideded the fourth day. I lost 5 pounds of fluid weight gain. Ten days after stopping predisone, I had a second onset of swelling and pain with 5 pounds of weight gain. I took 40mg two days and lost the 5 pounds and severe pain. I also lost depression that has been with me 45 years. I experienced elation sustained for the first time since I was 18 years old. I am 63, retired, blessed with a good life within a prison of secret depression. I cut the dose to 10mg per day and saw a rheumatoligist who ordered 15 blood tests today and continued the 10mg dose. the elation continues and is joined by high energy. Is this a gift from God or what? Fred

-- By fred872 | Reply | Private Message me

June 3th
2005
5:51 PM

My father is 76 and taking 120mg of Prednisone every onther day(5 pills) he was taking 6. The only real side effect is the days he takes the Prednisone he is in terrible pain on his left side under his arm. It is ore to the touch. We went to the Dr yesterday and they still have no clue. I just tied this together. He is taking it for kidney disease. It has completely stopped the progression but the side effect of the pain (which I am convinced is from the drug) is bad. We can count on every otherday to be a really bad day. He gets confused, wobbly on his feet and severe pain. So far the Dr has not statred this is a side effect. We are now waiting for the results of xrays to make sure no brokern ribs.

-- By plamont | Reply | Private Message me


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