I have a question about omeprazole, the medicine generally prescribed to protect the stomach lining from prednisolone side effects.
I take 7mg pred/day and have been prescribed 2x20 mg Omeprazole/day. I'm not a fan and usually take 1 x20mg omeprazole every other day. It can contribute to Osteopenia/osteoporosis, as far as I understand.
What do others think about Omeprazole? How much do you take, how often? What gut side effects have folks experienced due to prednisolone?
Thanks.
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Cyclo5
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I was prescribed with just 1x20mg, though in the end I couldn’t get on with it. Was there a reason they wanted you to have 40mg or just belt and braces? Does 20mg do the trick?
Some people aren’t bothered and you are taking only 7mg , though that would still have burnt a hole in me. However, if you decide to discontinue, do not just stop it because you can get a rebound acid production, so it needs tailing off. It might be worth asking a pharmacist whether you can just stop 20mg of the 40mg or not.
The dose depends on why you are taking it - reflux, for example, is usually 10mg in the evening. Otherwise the dose tends to be based on need.
I've never taken anything because of pred - haven't had problems. I did take something for a week while being given infusions of high dose NSAIDs - no desire to repeat either!
Thanks, I've never had reflux or other pred side effects since reducing to under 12mg. I did have stomach cramps when taking 20mg and down to c12/15mg, they would last about an hour then dissappear.
I avoided all stomach protection tablets, a pro-biotic Yoghurt with a teaspoonful of Manuka Honey (natural antibiotic) before taking pred and never had a problem.
I had GCA and started on 60mg and finally into remission 5 years later.
Omeprazole, read the side effects, one of the common ones is aches and pains.
Be careful on omeprazole I have ended up with acute kidney injury Stage 3. The tablet has caused inflammation in the tubes. I should have had blood tests to monitor my kidney function but along came the pandemic. Have had treatment now but nearly caused dialysis or worst case kidney transplant. Will be monitored for the rest of my life fingers crossed there is no further reduction in my kidney function!
No blood test August until end of January probably when the damage was done, next blood beginning of April when diagnosis swiftly followed! Yes pls nag drs re bloods
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Hi I’ve been on omepraziole too for R A and GCAj and many other drugs. About 4 years ago my doctor called me in as the hospital had warned him my kidney function was down to 40 percent. Nothing was ever done and as I hav
I have been constantly offered PPI's for years, well before being diagnosed (to my mind IMHO this is part of the Leaky Gut scenario viewed as potentially contributing to the vasculitis lying at the root of PMR) but they don't agree with me. I certainly don't want to be on them long term as there is sufficient evidence based info out there that this is not a good thing. A trained herbalist suggested I try Marshmallow Root powder which I take before each meal (teaspoon in a glass of water) to line the stomach and I find it incredibly effective.
Glad to hear someone else takes marshmallow root powder. I too use marshmallow root. I was so impressed by the anti-inflammatory effects I am now growing it in my garden. I have been using the leaves through the Summer, but haven't yet had the courage to dig up the root in case I kill it off. The whole of the plant is edible and has different uses. Tulsi is another impressively anti-inflammatory herb. I planted this in my garden too, but my little Italian gardener dug it out thinking it was a weed. Tusli is wonderful for the respiratory system as is marshmallow root. I have two cups of Tulsi tea every day now,
Great!! I order it as don't have the patience to do all the things herbalists do but it lasts. It has certainly been a great boon with my reflux etc. over the last year.
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