Reducing Pednisone

Posted by pmr52025 @pmr52025, Sep 16 9:59pm

I have been on 15 mgs of Prednisone since May. Recently my doctor had me reduce it to 13 mgs for 2 weeks and now 12 mgs for 2 weeks. I have started having some pain again. Pain in hands, arms and back. Is this normal when reducing prednisone? Has anyone had to go back up in mgs while trying to decrease their dosage?

Interested in more discussions like this? Go to the Polymyalgia Rheumatica (PMR) Support Group.

Profile picture for John, Volunteer Mentor @johnbishop

Hello @pmr52025, I would like to add my welcome to Connect along with @beauty44, @st1300 and others. I think anyone that is struggling to taper off of prednisone might find the following discussion helpful.
-- Hello How to Slowly and Safely Taper Off Prednisone but ... no set rules.
https://connect.mayoclinic.org/discussion/how-to-slowly-and-safely-taper-off-prednisone-but-no-set-rules/
For both my occurrences of PMR I kept a daily journal of my level of pain when I woke up in the morning and my dose of prednisone for that day. It was recommended by my rheumatologist. When it was time to taper to the next lower level, I either went up half of my previous taper down or went to the next lower dose in my tapering schedule depending on my pain scale being less than 2 which was my acceptable level of pain that I could easily deal with.

There is an upcoming webinar that you might find helpful - Polymyalgia Rheumatica: Closing Gaps in Diagnosis and Disease Monitoring tomorrow, Thursday, September 18 at 6:30 PM Eastern.
Topics covered:
- How PMR is diagnosed and tracked
- Why some patients are misclassified or overlooked
- The role of patient experiences and reported symptoms in care
- Gaps in today’s practices and what can be done to close them

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@johnbishop thanks for info. I just watched. Wish o had signed up so I could get on their email list, etc!!

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Profile picture for kare1 @kare1

@johnbishop thanks for info. I just watched. Wish o had signed up so I could get on their email list, etc!!

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@kare1 if you go to their website you scroll down and there is a spot to enter your email address to sign up for their newsletter - https://creakyjoints.org/

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Profile picture for John, Volunteer Mentor @johnbishop

@kare1 if you go to their website you scroll down and there is a spot to enter your email address to sign up for their newsletter - https://creakyjoints.org/

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@johnbishop

Great !! Thanks.

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I started Actemra 6 mos after diagnosis and had been on as much as 40-60 mg Pred since my symptoms & diagnosis. I’m tapered off Pred now but remain on Actemra after 1.5 years. I don’t see how it’s helping my discomfort much, but my lab numbers are good now. Rheumy wants me on it longer , but no Pred !

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Profile picture for aflik @aflik

I started Actemra 6 mos after diagnosis and had been on as much as 40-60 mg Pred since my symptoms & diagnosis. I’m tapered off Pred now but remain on Actemra after 1.5 years. I don’t see how it’s helping my discomfort much, but my lab numbers are good now. Rheumy wants me on it longer , but no Pred !

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@aflik
Actemra blocks one source of inflammation, IL-6. You must have additional kinds of inflammation that are active. I started Actemra about 6 weeks after diagnosis, and I've been taking it for 14 months. I've been off of prednisone for about 6 weeks. I haven't had any symptoms of PMR or GCA since I started treatment 15 months ago.

You could try Rinvoq. It works differently than Actemra, and is approved to treat GCA.

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Profile picture for aflik @aflik

I started Actemra 6 mos after diagnosis and had been on as much as 40-60 mg Pred since my symptoms & diagnosis. I’m tapered off Pred now but remain on Actemra after 1.5 years. I don’t see how it’s helping my discomfort much, but my lab numbers are good now. Rheumy wants me on it longer , but no Pred !

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"I don’t see how it’s helping my discomfort much, but my lab numbers are good now. Rheumy wants me on it longer , but no Pred!"
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@aflik
I still have "some discomfort." I was on higher doses of prednisone too. I spent a long time in the 40-60 mg range, Then I spent an even longer time in the 20-40 mg range. I finally got stuck on 10 mg when Actemra was started. When you consider all the flares I had tapering off prednisone --- Actemra works so much better for me.

Considering I was on Prednisone for PMR for more than 12 years, I am very happy to accept "some discomfort" in exchange for being off prednisone. More importantly, I haven't had any flares in almost 5 years since being treated with Actemra alone.

My medical records list "long term Prednisone use" as a problem. In parenthesis, long term is clarified and it says "decades." I look at it this way --- Actemra must be doing something because otherwise I would not be off prednisone.

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Profile picture for jeff97 @jeff97

@aflik
Actemra blocks one source of inflammation, IL-6. You must have additional kinds of inflammation that are active. I started Actemra about 6 weeks after diagnosis, and I've been taking it for 14 months. I've been off of prednisone for about 6 weeks. I haven't had any symptoms of PMR or GCA since I started treatment 15 months ago.

You could try Rinvoq. It works differently than Actemra, and is approved to treat GCA.

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@jeff97 thank you!
I don’t have GCA. I know Actemra is primarily used for GCA and off label for PMR. I’ll be discussing the continued use of Actemra with my Doc during my next visit. Rinvoq seems to have some bad side effects.

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Profile picture for aflik @aflik

@jeff97 thank you!
I don’t have GCA. I know Actemra is primarily used for GCA and off label for PMR. I’ll be discussing the continued use of Actemra with my Doc during my next visit. Rinvoq seems to have some bad side effects.

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@aflik
Actemra can have some bad side effects too. I take it, but my rheumatologist lists it in my chart as a major risk.

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