Prednisolone symptoms and conditions

I've been prescribed Prednisone since April and just recently experiencing hair loss (I'm Female)

hair loss after prednisone?

i took 60 mg of prednisone for 1 month for a kidney inflammation. i tapered down for months and finally have been off it completely for a few weeks. i did lots of natural things and really had no side effects- my face did get puffy when i was tapering, at about 30 mg but that's gone now. and my lip hair came in fuller but it's pale blonde so it wasn't too much of a bother

however, suddenly my hair is falling out like crazy. i took advair for many years (only 1/2 dose) and didn't connect it with my hair thinning until i started reading this site. i weaned myself off advair and noticed soon after that my hair loss in the shower was minimal

then i went on the prednisone and i was still fine. has anyone noticed hair loss after stopping prednisone? will this stop after a while?

I have been on prednisone since I was two years old (I am now sixteen) because I have Autoimmune Hepatitis IIa. I would like to point out that there is still a life worth living being on prednisone, maybe I say this because I do not know life without it, but at least we're alive! Last year I had a flare up of the AIH and had to 6x my dose of prednisone. It sent me into a spiraling depression of constant sleep, crying, hopelessness etc....but I made it through. Just PLEASE keep hope that things would get better, because I know what it's like being on the dreaded drug better than most.

I was on Prednisolone for 6 weeks and finished them 2 weeks ago....I gained 18lbs in weight, which I still haven't lost..The swelling in my face has started to decrease...My stomach is so bloated, I look about 6 months pregnant and cannot get into any of my Jeans..I suffer permanent indigestion and constipation, plus discomfort and aching in my chest and around my heart..I have booked to see my GP again this week as I feel so uncomfortable.

I wrote a post few days ago about Singulair and how great my daughter is doing since she started to take this medication three months ago.
Then I started reading about all the side effects that other children had because of Singulair. I GOT SO SCARED!
So scared that last night I stopped giving Singulair to my daughter.

From January to September my daughter had asthma every other week. She was put on steroids (prednisolone) every time she couldn't breath. Then in September the pulmonologist said we have to take control of the situation because so much steroids can damage a little body.
She made me feel I had been a terrible mothers since I always refused to give her singulair.
She convinced me and then I started Singulair, but now I feel worst because I have the feeling I am giving poison to my daughter even if her asthma is under control.

My 7 years old stopped Singulair 12 hours ago, I do not know what is going to happen now. Of course I cannot call the pulmonologist anymore in case my ds gets bad.
Somebody here said that she is giving her son Nordic Naturals Fish Oil, Culturelle probiotics, vitamin c, and changing his diet - increased magnesium and decreased dairy.I will love to have more information about this alternative way of controlling asthma. I do not remember who wrote this post. If there is a web site of a doctor I can contact i will do right away. I live in New York.

I need help. Thank you so much.

I have been on Prednisolone about 4 times in recent years. the highest dose was last year when i was on 80mg reducing weekly by 5mg. I have had most of the side affects you all talk about above. I have severe colitis so the side-effects of this drug are something i have to put up with. at the moment i have all the classic side-effects i usually get, rapid hunger, swelling to my face (moon face), neck has layer of fat, swollen back (buffalo hump), bruising easily, horrible taste in my mouth, swollen stomach. the one good side effect is it gives me lovely smooth skin lol. anyway the point of my post isn't to rip this drug appart as i have to say for me its a wonder drug and this time has prevented me from having my bowel removed! from personal experience once you finish the steroid treatment after a few weeks you'll notice the swelling go, my hunger usually fizzles out quite quickly (altho i have a large appetite in the first place!!) none of the side effects are permanent, so please all rest assured you will go back to normal just try not to put on too much weight while on the drug.

I was put on Prednisone for my COPD. Right after starting a 30 day script (I don't remember the dosage) I started experiencing SEVERE muscle cramps. Legs, feet, hands, abdomen, ribs, back. It was the most terrible experience I have ever had and I refuse to take it again. I also gained 30 lbs in 30 days. Which I have had extreme difficulty taking back off. I am now, two years later, experiencing great difficulty with my knees. I believe that I will always suffer the side effects of this, yet another, wonder drug. The wonder is how many people's lives is it ruining...

After reading all the horror stories on here, me and my husband soon began to realize that we were having a lot of the side effects listed here and not listed on my son's actual Singulair prescription. The side effects my son had were behavioral changes, irrational behavior, inattentiveness, not able to stay on task or stay still -- in fact he broke his arm twice being so hyper, yelling, screaming and just plain mean.

We took our son off of Singulair as a trial for a few days. Immediately we began to notice differences in his behavior. He wasn't as agitated and quick to yell or get angry. (He's only 5 years old). He actually would be listening when we would speak to him. He would sit calmy and read books and the one huge thing he would do was look at us and smile. He even said to my husband once, "I love you Daddy," which just brought tears to our eyes. I never realized what a Singulair fog he was in and what it did to him. Here we were pretty close to getting him evaluated for ADHD or even Aspergers. So now we're in the same boat as others that are searching for other asthma meds to give my son. Right now we have gone back to Pulmicort, Xopenex, Nasonex and Allegra. I'm so glad I read this forum because I was desperately searching for answers for my sons behavioral issues. Oh, by the way he was on Singulair for 1-1/2 years.

You people are freaking me out. I just started today with my first dose of prednisone for my first bronchitis diagnosis. I've been sick for 3 months and thought this would be a good med for me to rid the coughing. I'm starting to reconsider taking any more if all I can expect is long term adverse effects. I took this once before years ago for a severe skin allergy. I got the psychosis initially but then adjusted the dose. Then, I would get euphoric and full of energy, like being on a stimulant. I had no idea the round face thing was due to this, I thought I just ate too much while I was home sick for 2 months. I think I'll try the herbal alternative route. If it works, I'll write again and let y'all know. Thanks for all the comments.

I had been on a prednisone dose pack (not too strong??) about a month ago for a neck injury to take away some inflammation. No side effects to mention and my neck felt tons better. Yesterday I went back to my dentist after 5 days of pain from a root canal. He put me on a prednisone dose pack saying there was some inflammation in the bone, very common, and the prednisone should take care of it. I took my dose yesterday, didn't sleep well (common side effect it seems) but then today my heart is racing and feels like it skips a beat. I have read this happening to folks on much higher doses, anyone have this kind of side effect with 20 mg/day?

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.

Hi All

Don't know what to do.. Been daignosed with Pneumonia, completed 7 days of Amoxicillan 500mg and now on day 4 of Clarithromycin 500mg, and 7 day course of Prednisolone 40mg per day.
Like everyone else, the most horrific taste in my mouth tried everything to rid of it. It is Sat night and I am NOT going to take my next dose of Clarithromycin as it is upsetting me so much. I will have to wait until Monday am to speak to my doctor and hopefully he can give me something else. I am still struggling with pneumonia however I will take the risk. The bad taste, and upset tum must be the worst side effects ever what do you all think? The companies surely mus be able to something about this and put us patients out of our misery!!

hi, Finished a 6 day pack of Prednisone and am so very tired. I feel a bit sick and have hot/cold flashes. More than the normal for my age. I do not feel energetic. I don't know if it is the winter and gray sky doing it to me, but I don't think so. I feel so blah. Could this be from the Prednisone?
Thank you in advance for your help.

Hello EveryOne out there...OK OK....

Now Why have I been out of touch since Sept 14th.... 2007???

I have been VERY VERY ill.....

Y'See, I went to see this new Doctor (Quack) for continued pain in my chest (sternum) area....that I have been having trouble with all Summer. (Severe Costochondritis/Fibromyalgia) By Sept 14th, this Quack who claims to be a Doctor had given me this prescription for Prednisone pills (20 mg each)....with orders to take mega doses of this toxic poison in order to combat the pain I was suffering. I was so desperate to get out of pain that I went ahead and filled the prescription and started taking the pills that eventful Friday night. I made the fatal mistake of trusting this Doctor!!!

If I had any sense God gave green apples I would have researched this a little before taking this medicine!! I would have run like all heck in the opposite direction!

I had been taking these reccomended large doses for approx two weeks back then per Doctor 'Quack's' order.... I have been hooked after the first week....and now currently desperately trying to get off of it with only marginal success!!

I have been on this Prednisone crap for some 49 days, currently and desperately trying to get off of it....with terrible side effects!! I have experienced every side effect known to the Devil himself and even discovered some new ones that I never knew was possible!? Case in point! I can't sleep night after night without terrible withdrawals all night long!!! I am forced to contend with them every night here. Not to mention I fight the withdrawals all days long too. I have this inept doctor and I am sorry I even went to him in the first place...!

The withdrawals I am now getting are harder to deal with than the original chest pain itself!!! Not to mention even eating the so-called 'wrong' foods sets off even more withdrawals almost immediately. I am now extremely sensitive to light and the sun~ not to mention.....noise....and stress....

I am much sicker from this Quack Doctor's so-called "HELP" than I ever was before....

I don't mind saying his name and trying to steer everyone away from this jerk Doctor here in Las Vegas who takes advantage of people in pain when they are desperate by feeding them toxic poisons and passing the poison off as something harmless thats gonna help them??? Just ask me who he is and I will tell you. I have no qualms about it....

Bottom line is I have spent this last month trying to get off this crap and I just found out that the withdrawals may bother me up to a YEAR after I take my last dose of this crap poison!! I have been going thru H***!!! A nightmare I would LOVE to pass onto this Quack who pretends to be a doctor!

I am down to about 7.5 mg per day now from about 180 mg that he gave me originally Sept 14 2007. Believe me this was not easy thing for me to do. I went "Toxic" on this drug weeks ago and it has affected my ability to process, think and reason properly. I feel like part of my mind is now missing or went on permanent vacation!! Dizziness,feeling like I'm gonna pass out, Brain Fog and Mass Confusion is the order for the day~depending on the time of day???

"The side effects of prednisone include adrenal suppression, which can occur with periods of prednisone use to surpass seven days. Adrenal suppression refers to the body’s inability to synthesize natural corticosteroids, resulting in a dependency on the prednisone taken by the patient. This is why doctors do not recommend the cessation of prednisone when the patient has taken it for longer than seven days. They reduce the dose gradually over a few days in the case of short-term prednisone use, and over weeks or months in the case of long-term treatment. Stopping prednisone treatment abruptly can cause the life-threatening Addison’s disease, in which in the body no longer produces sufficient amounts of adrenal steroid hormones"

I want to SUE this Doctor for making me this sick!!!!!

SDR

GRRRRRRRRRrrrrr!!!!!!!

I took this medication seven years ago. After a couple of days I broke out into hives. When the initial Hives went away I kept itching. Then, the itching began to spread all over my body. I have been turned away by many doctors who wished me luck and said they were sorry but they couldn't help me. Since then, I have become a science project for doctors. I have taken a number of medicines to calm me down and an assortment of creams and lotions. One spray that takes the itchy hives away for awhile is CLOBEX. It's very expensive. It costs me $250 a month (out of pocket). The only medicine that relieves the condition for about a week is prednisolone (another drug that's not so great for you). I now take that once a month for one week’s relief. Each night, I have to scold myself in the shower to relieve the itching for a few hours so I can go to sleep. I'm currently at a new Dermatology Clinic. Guess what they prescribed for me? CEPHALEXIN, the drug that caused the poor quality of my life I now have. Doesn't anyone listen to the patient? The only best medical friend I have is my Primary Care Physician who has greatly supported me all these years. I pray that someone may read this and I have an answer me.
If you have not yet taken CEPHALEXIN, think about it long and hard. It's not for everyone and MAY not be for ANYONE. If you've read this far in my note, I consider you a new friend.

Someone please help!!
Still Itching in New Jersey.

Was on Prednisone 2 years ago for respiratory problems 30mg. Gained 25 pounds, fat face, felt tired, etc.

However 2 years later, after weaning off Prednisone my muscles ache, joints are most always stiff, esp. hands plus my feet feel numb and my short term memory has not returned to normal----does any one else out there have similar problems. What can be done?

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 was prescribed cephalexin for infection in my head and after the third day of using it I broke down into hives and started itching throughout my whole body.

I've been on it for about 4 months. It does seem to help but I've had problems with steriods (prednisone) taken as a result of colitis.
In the case of Advair I get the hoarse voice and sleeplessness.
I'm also concerned about the long term use of this drug on my lungs. It is a steroid. I have diffuctly in breathing, especially taking a deep breath.
Does anyone know of any studies on how safe Advair is for your lungs or the rest of your body.We have had very bad experiences with Steroids.

my 17 year old son needed a hip replacement as a result of steroids (not Advair) this summer.
BEWARE OF STEROIDS.
lets find out about Advair.
Does it have any adverse steroid Affects??
please let me know.

Thank you

Peter W
******

i'm asthmatic and used to weigh 10stone, now i weigh 25 stone, i was on prednisolone for 4 yrs and 40mg a day but my doctor 4got to tell me that the tablet had a side effect of weight gain, i was put on the tablet in 1989 and put 8 stone on within 18 months, now i have arthiritis in my knees, back and alot of pain in my hips, but due to my weight i have alot of other problems now, and i can't exercise, and i don't over eat either, but can't lose the weight, i'm only 35 and feel my life is over thanks to prolonged use of prednisolone and a doctor who failed to see what was happening,

Hiya. I was on prednisolone for 8 months 40mg a day. I have been of the steroids for a month now and cnt beliveve how much weight i have piled on. I don't eat excessively but have put on a stone and half since taking this horrible drug and it wnt shift regardless of excercise and healthy eating. I'm defo going to try some of your suggestions, hopefully the moon face and swelling may satrt to decrease. Fingers crossed eh!!

Hi, i was diagnosed with Crohn's disease and put on Prednisolone 40 mg/day starting June 1 of this year. I'm now down to 5 mg/day. My Crohn's symptoms are better but i have other symptoms that bother me a lot. Can't sleep at night, very weak in my legs and major depression. I'm supposed to see my doctor today. I'm afraid he may ask me to go back up to 10 mg/day. I just want to get off this stuff. I will appreciate any suggestion or help anybody can offer.

Regards,
Reza

I was on prednisone from 1998 - 2000 for a kidney disease. At one point I was taking 120 mg a day for 5 weeks. It stopped the progression of my disease my. They slowly weaned me down to 10 mg a day. I went from 155 lbs to 215 lbs. in about 2 months, but I ate less. It was like being "fat." It was like being filled with air. My face looked awful. When I smiled, my eyes disappeared. After I went down to 90 mg, I was put on cytoxan (chemo), so not only was I huge, I was also bald (real attractive) Now, I am somewhat back to normal and my disease is in remission, not cured however. The only side effect that I have that is a life long reminder of my battle is these horrible stretch marks. I have several of them. They range in width from 3/4" to 2" and when they first started appearing it felt like I was being torn apart, and they would bleed. I have them on my sides, on my belly, and under my arms. I was not a large person before. But the excess skin makes me feel so self conscious. Does anyone else have "scars" this bad?