PredniSONE and pills

Hi

I just started taking 20mg of Prednisone for a shoulder injury. So far I have all but loss my appetite, which sounds strange to me since my doctor told me to expect to gain weight very quickly. I have also loss my need to sleep. I was up from Saturday 11:15 am morning the first day I began Prednisone and wasn't able to get to sleep until Sunday night around 10:00pm. I'm sweating like I'm constantly being rained on, it is so darn annoying. I also started to lose my voice last night and then again today, is that normal with is drug? I'm so full of energy all I do is clean our house, work out in my flower beds, etc. I'm kinda of scare of this drug and I'm glad I will be off of it next Tuesday unless my shoulder isn't better when I start physical therapy tomorrow. I wish you all the best while you are taking this drug.

Keep us posted on how you are doing.

Marlene

My son is suffering from psychosis because of prednisone. He had severe poison ivy and was given 10 day course of pills that tapered and a shot. Since then he has been in the psych ward for a week , released given respirdal and lithium. After 3 weeks we tried to wean him from the respidal but the psychosis came right back. ;He is 17 and never had any symptoms of psychosis or mania before. He has every symptom now. BTW his psychosis did not appear until he was finished with the prednisone for several days. Will he ever recover?????

My husband was stung by a wasp. He had a major reaction of hives and fainting spells. Naturally we went to emergency where the doctor prescribed.. you guessed it.. PREDNISONE !! sigh. He was told to take it only the next morning of his attack as the prednisone would make him too irritable to sleep. He woke up the next morning and all his rash was gone and he was feeling like a million bucks. NO more side effects from the wasp sting. We were always wondering WHY he needed to take prednisone for a wasp sting but wanting to listen to our knowledgeable and GOOD doctors, my husband took the prednisone. He was told to take 10 5mg pills in one shot, therefore, 50 mg. per day and then eventually wean himself off. Well, he took but the first 10 and within the 1/2 hour he developed an even greater reaction to hives than the day before. He became very agitated and moody... We drove back to the hosp. only to see the same doctor who'd tell us that he didn't HAVE to take the prednison if he didn't want to and that he was SURE that the prednisone had not caused this latest and worse reaction !!
For crying out loud. This is the year 2008. Couldn't the doctor have told us ahead of time that if the symptoms disappeared before even filling in the prescription ( which is what happened in this case ), THAT He should never have taken any drug? Prednisone is a killer. I know.. My mom DIED because of this darn drug only to find out that they were treating her for a disease that she probably didn't have after years of using PREDNISONE. These poor older people think that the doctors are GOD and that they have to listen to their every word. My husband, on the other hand, has thrown the drug away after just ONE USE. PLEASE, people, find other doctors and solutions and get second opinions.

Hi all. I would just like to agree that PredniSone sucks but it is the best out there for these diseases especially the auto-immune diseases. Drug companies do not make any money on prednisone because it is generic and there is no patent. I know I picked up 98 10mg prednisones yesterday for $5.00. Believe me when there is a better steroid that works as well and has less side effects it will be available to us all. It will cost tons but it will be sold. Researchers have been working for so many years trying to find an alternative, some have been found but do not work well enough. As bad as the prednisone makes us feel it does work on the diseases. You always have the choice to say no - that is why we should all have a health care power of attorney - just remember that when you decide not to take the prednisone you are agreeing that the disease may worsen and may be life threatening. I hate to sound so morbid but patients must be informed. When you are at the physician ask about the side effects, ask if they can give you something to counteract any mood swings, ask what lotion is best for the itchy skin (AmLactin works well for me and is over the counter). Also, my physician advised me yesterday that the side effects are worse on women due to our precarious hormones. I have told my husband to just stay out of the way and don't piss me off because I am not sure how this next 7-8 weeks is going to fare for him. I am 4ft 10in 110lbs and he is 6ft 1in 200lbs and believe me he is scared for his life. I am using prednisone for my ulcerative colitis so now that I am feeling better physicially I can return to exercise and that has definitely helped. So has turning up the music really loud and dancing and singing poorly. Yelling at the tv helps me whether it be politicians, soap operas or idiots on game shows who get the wrong answers. I also have been keeping a journal of all the rage I have and what kinds of things I could do to people who keep getting in my way at the store, on the road, in line at the pharmacy - I guess I need to put that in a safe place so it can't be used for evidence :}

I've been on in a little over one day. The 6 day treatment. 5mg pills-6 the first, 5 the second, and so on and so forth. I have been SO HOT! I didn't sleep for very long, and woke up a couple times in the middle of night burning up. For me, the mental side effects have been HORRIBLE. I'm a 20 yr old fairly healthy female. 5'3'' 110 lbs. I have had unbelievable depression.... really really irritable and angry. I've just felt like hitting someone 24/7. I don't want to talk to anyone, I just want to sleep, I can barely keep my eyes open. I don't know how I'm going to take 5 more days of this. I also experienced the extra sensitivity to heat that others described. I read online that photo therapy... or sun exposure will help speed up healing and can be used alongside prednisone. I just really want this all to be over with. I look like I have the plague, and I feel worse than I look on the outside. Every little stress or worry just makes me want to end it, though I know that that isn't the answer. I'm a Christian, and I'm just going to pray about it. God will take care of me. I'm BURNING UP AS WE SPEAK! I've also been extra thirsty and my skin feels so dry!

my sister was put on Prednisone for a inflamed heart and fluid around the heart, she started with 6 pills a day at 5mg for 7days, then 5 pills for 7days then 4 all the way down to 1 a day. When she got to 1 a day the EXTREME chest pains came back she was in and out of the hospital so many times it was crazy, she was then put back up to 6 a day and slowing get weaned off, however her side effects are insane, major swelling, moon face, weakness, INSOMNIA bad, rashes and bruzes are appearing everywhere, coughing a LOT, sore throat, foggy vision, shortness of breath, thats put it this way she is a MESS and to top it off her husband of 24 years passed away on April 30th, 2008 with a massive heart attack at 47 years old, she feels like she is going to go CRAZY, if anyone has any suggestions it would be so appreciated. Thank you SAD SISTER!!

First time taking Prednisone, I was prescribed for an injured rotator cuff. All it took for me was one 20mg pill before bed. I only slept for about an hour and a half in that time i experienced extremely vivid nightmares i then woke up for the rest of the night with bouts of paranoia. for some reason i thought i needed to have my gun under my pillow, i kept thinking someone was going to break in my house.(this is not typical behavior for me) Stoped use of the pills immediately.

Hi all,

Well since my last post on April 23rd at 5:24, so far I have been coughing a lot. My throat is so sore just from coughing, I've been coughing up thick yellow mucous. Going into the 3rd day being on Prednisone, I couldn't take it anymore. The doctor originally requested me to take 3 pills a day for 4 days, then 2 pills for 4 days and then 1 pill for 4 days, I decided to change it. I took 3 pills for 2 days, then 2 pills for 2 days and 1 pill for 2 days, I couldn't take the side effects of severe insomnia, coughing, very dry mouth and shortness of breath going into the 3rd day. Since being prescribed Prednisone on Monday, I found myself today to be miserable. Whenever I cough my head feels like it's expanding, soon to explode and my brain hurts, I fear coughing because my throat hurts as does my body. I don't ever want to take this drug again, it's toxic. As for me now, I plan on going and laying down and sleeping like Rip Van Winkle and make up for lost sleep I didn't get during the week. Only being on this stuff for one week definitely made me sympathize with many of you who used it for years, one week was a rude awakening I don't ever want to experience again. Now I am going to go grab my stuffed bunny and crawl in bed for restful sleep.

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.

I started Prednisone 2 weeks ago and gradually started having leg cramps. They have gotten worse over the last couple of days. They are in my ankles and feet and I have to get up several times a night just to sit until they relax. We plan to decrease the dosage in two weeks, but this is most annoying. Of course, it's far better than what I was experiencing with pain and sleepless nights and had gotten so I could barely move. My hands were swollen and tight, my arms ached with every move and movements were very limited. My bones in my feet felt (and sounded) as though they were shifting around when I got up to walk. My knees were weak. I was just diagnosed with polymyalgia rheumatica. I feel 70-80% improved. Just wondered if anyone else has had these symptoms on Prednisone. It didn't do this with the dosepaks.

I have read some of the board and would like to know if anyone else has had prolonged side effects after being off Prednisone for almost a year. I think Prednisone caused all my current health problems. Was on the higher dose 5 day plan for a severe inner ear infection. I stopped taking it after the third day cold turkey, which I know was wrong because of blurred vision and stomach distention so bad I thought I was going to burst (almost the same as when I was pregnant). The first 4-6 weeks of stopping it were pure _ ell. So many withdrawal symptoms. I went to my doctor and he said I couldn't possibly be having all those symptoms from the Prednisone since I was only on it three days (but it is the regimen where you take the higher doses/multiple pills in the beginning and then it lowers the dose each day). Every few days it seemed I was having something new happen - heartburn, sweating, headaches. Then my thyroid function began acting up (hypothyroidism) and glands seem to swell with my monthly cycle. I started having a daily dry throat. All my symptoms seem to be on my right side: blurred vision, dry throat, swollen lymph glands, ear pain, groin swelling. It is one month shy of a year when I originally took the Prednisone and nothing has decreased, only new symptoms appear. My doctor keeps treating each symptom individually and won't look at the whole picture. I tried acupuncture and it didn't help. Any suggestions/comments?

I started taking Prednisone in late November for inflammation of my lungs, a complication of influenza A. I started at 50 mg daily, then went to 75, then was hospitalized and went to 160 intravenously. After about a week, I was reduced to 120 then 75 by mouth a few days later. After 15 days in the hospital, I was released only to come back two days later with internal bleeding. I was released two days later and my doctor knocked several days off my withdrawal plan. About midway through all this, I started having a constant mild headache. After my second release, the headache started to get worse. The headache became debilitating and I spent some time in the ER where codeine helped. (I'm allergic to morphine which would have been their choice). The codeine helped for a day or two, but when I got to 60mg of codeine with no effect I gave up on the pills. My doctor gave me some sort of anti-inflammatory shot which helped.

I've been off Prednisone now for over a week and still have a constant headache, but most of the time it's not bad and only moderate at times. On average I see a gradual improvement.

I have had increased appetite and energy (in the beginning) followed by face and neck swelling, headache, nausea, blurred vision, internal bleeding and large muscle weakness.

I know that I needed something to stop my lung inflammation, but the cure has been worse than the disease at this point.

Hi!
I have ulcerative Colitis. I had a bad flare up since Thanksgiving 07.I have been on Prednisone since the beginning of Dec.07. The first 3 days it was giving to me by IV every 6 hrs.I was hospitalized due to tremendous blood lost. After this my doctor put me on 60 MG a day. 6 pills of Asacol and I also was on ennama with Cortisone which totally almost killed me. The side effects were sooooooooooooo bad,let say I had them all.Right now I'm dealing with the side effects of the evil Pill " Prednisone" Moon face and this awful bloating in my upper abdomen, tiredness, no energies, heavy legs. It makes it really hard for me to get out & around.I hope my doctor will get me off this Prednisone. Not only messes it up your normal living no it also makes you look like a ugly bulldog! I hate it!

I agree, for me this is a horrible drug! This is the 2nd time my allergist prescribed it to me (last time was this past summer and I had severe panic attacks and thought I was losing my mind) this resulted in me returning back to my GP and him putting me back on Paxil (which I had been off of for a year). I was extremely reluctant to use this again but thought i might be able to manage it this time (with the help of Paxil).

My allergist prescribed Prednisone to me 2 weeks ago (5mg 3x's day for 3 days then, 2 2x's day then 1 for 5 days) I made up until the last 3 pills. I had severe brain fog and felt like I was floating through space. I couldn't even remember driving to work and parking my car! Extremely fatigued (I have diabetes (which is under control, but I had to keep checking my bg because I thought my sugar was dropping to low). Now, within the last week of taking the Prednisone I have experienced aching in my kidneys and I think I have a kidney infection.

Can Prednisone do this to you??

I am calling the doctor tomorrow. Today is the first day without Prednisone and I feel like I am totally out of it - really spaced out, dizzy, panicky and a bit nausea.

How long does it take for you to get Prednisone out of your system?

I was prescribed Prednisone for sinusitis and bronchitis. By day three I noticed I was taking 6 pills versus the 3 prescribed. I called the pharmacist and they recommended I take 1 for each remaining day. I declined, because by then I was experiencing a lot of leg pain. I thought I had a blood clot. Now that it's day 6 I've experienced muscle and bone pain throughout my body. Last night while lying down I felt lightheaded and like I was going to blackout. My legs are weak, I feel like I'm having an outer-body experience, and I'm restless. I've gained a little weight and have a dark red/purple rash on my chest. My stomach is still bloated, but does not hurt. I hope this ends soon. God Bless you All!

Along with Prednisone, I am on Methotrexate and now a slightly enlarged spleen that has reduced my red platelets to only 75,000

If my Doc takes me off of these pills for my RA, what kind of pain will I be in and is there any alternatives to Prednisone and Methotrexate. I've been on these for 5 years now.

I was prescribed 42 pills (20 days) of 10 mg Prednisone which I am to take beginning with 4 pills for four days and steadily decreasing every four days down to four 1/2 pill the last four days. I took my first dose yesterday and was told to drink lots of water. I do not wish to gain weight nor have a moon face. My doctor does not feel this will affect me in that way, but may have water retention (swelling). I am 73, and this regiment of Prednisone was prescribed to decrease inflammation due to a possible siatic nerve problem, which is causing extreme pain in my left leg. The pain is excruciating when I get up in the morning but eases down by mid morning with some pain all day and some nights if I move just the wrong way.Does anyone have a suggestion for the best foods to eat and what to avoid? I read that grapefruit juice may be beneficial.