Side effects of Prednisolone - Crohn's and Colit...

Crohn's and Colitis Support

5,287 members1,691 posts

Side effects of Prednisolone

jostafford0 profile image
12 Replies

Hi all,

I've recently had a severe flare of UC and was in hospital for a week on hydrocortisone shots. I was discharged a week ago and I'm now taking Prednisolone but I'm having horrible side effects of shaking and lethargy. Has anyone experienced these side effects as my GP said it isn't normal to feel like this on Prednisolone? I also felt very fatigued on the hydrocortisone too but didn't shake.

Any advice welcome

Jo x

Written by
jostafford0 profile image
jostafford0
To view profiles and participate in discussions please or .
Read more about...
12 Replies
tonyputt profile image
tonyputt

hi yes i have had this side affect from prednisolone as i have CD my GP gave me a mild anti depressant which helped . prednisolone is brillant at controlling but not so nice side affects . You may find you will want to eat for England and very restless but it does decrease when you lower the dose .. i hope this helps

jostafford0 profile image
jostafford0 in reply to tonyputt

Hi Tonyputt,

Thank you for replying - it's reassuring to know that other people have experienced these side effects although they are horrible. My GP didn't have a clue!

Jo

tonyputt profile image
tonyputt in reply to jostafford0

Your very welcome .

i was on these steriods for way too long . but an anti depressant will stop the shaking and any mood swings you may have from using the steriod. you are very right the side effects are horrible and they do not taste very nice either unless your lucky to have coated tablets. You should also have calcium tablets as well .

But they do work very well

willow24 profile image
willow24Administrator

I ended up with steroid psychosis - not pleasant at all. that was along with the fluid retention, esp knees so walking was really painful, heartburn, palpitations, not sleeping the list goes on. It totally messed up my metabolism too so was unable to lose any weight afterwards - did when had flare up, just to be put back on steroids again. I'm unable to tolerate them now so rely on different meds.

Hi,

I had a bad reaction to prednisolone too. I had uncontrollable shakes and heart palpitations to the point where one night I thought I was having a heart attack and was taken to emergency department. I also had really bad anxiety and mood swings. So I was quickly taken off it and changed to Budesonide. I've found Budesonide is working well for me with no side effects but it's not covered by the pbs so it's about $130-$160 depending on where you go to purchase this medication. I hope you feel better soon!

billi profile image
billi

Hi Jo , I was on prednisilone for almost 7 years , this was back 25 years ago when evenn doctors hadn't heard of Behcets. What I discover is ....it is only a plaster in that once you take it off everything comes back again. Also when you restart it you have to take a higher dose each time and it is only hiding the symptoms not helping to eliminate them. No I dont know your situation but I now have on my medical notes...NO steroids or tramadol. There are other and better meds out there such as Colchicine , azathioprine and many more. I suggest you speak with your consultant and find out your options. Hope this helps

Billi

billi profile image
billi

Sorry I thought I was in the Behçet's disease section so the medicines I mentioned may not be suitable but the prednisilone facts remain the same.

Billi

jostafford0 profile image
jostafford0

Hi Stuart, I used to just drink tap water but have bought mineral water from Liddel now. I'm thirsty all day so I do drink a lot of fluids including decaf tea & coffee. I haven't heard of consuming silica so will need to research this - thank you for bringing up the topic. Regards Jo

jostafford0 profile image
jostafford0

Hi Stewart, I researched Silica and was impressed by the claims so ordered bamboo silica capsules to try. I'm still on steroids - down to 15mg now and have horrible side effects every time I drop down. I'm still shaking and tired so really hoping this goes away when I eventually stop.

jostafford0 profile image
jostafford0

I must have sent my message at the same time you did lol! I've been taking the bamboo silica for about 4-5 days now so will wait and see if it improves my bowel movements. I am always thirsty and drink loads, I started buying mineral water (Buxton) as tap water wasn't doing me any good.

Bazmack profile image
Bazmack

My hubby started at 40mg of prednisolone reducing 5 mg every 5 days. At one point he was so dizzy and went very grey I called an ambulance as he has heart problems as well. We saw a really good doctor at A & E who said his steroid dose was too high and we were told to reduce by 5mg every 3 days. He has now finished the course and the dizziness has gone but he still eats for England . He suffers from CD and Lymphocytic Colitis and was very ill a few months ago before he received his diagnosis so he needs to put some weight back on. He went from 105 kg to 66kg in 2 years. Yes he was overweight but went to being malnourished because of CD and a useless GP who told him ‘you are an adult, eat’.

Bec_789 profile image
Bec_789

I didn’t have shaking, but did experience tiredness and my heart rate certainly felt strange whilst on it too. The worst thing for me was the brain fog- felt like I wasn’t functioning right at all.

You may also like...

How long for prednisolone to take effect?

put on prednisolone (40mg 8 week taper). I've been on it before but this time the side effects have...

Colonoscopy side effects

I had a colonoscopy earlier this week . I learned on friday that it showed i had collagenous colitis

Sulfasalazine side effects? UC and Enteropathic Arthritis

hours a week over 3 alternate days and seem to spend my days off recovering. I know that fatigue is...

Rectal prednisolone (UK)

help with ulcerative proctitis. I'm suffering from an extended flare, and the local IBD clinic...

Going to start prednisolone steroids 😳

the side effects are scary but I just want to have peace of mind and more control. Any advice...