Ringing or pounding in ears
Is anyone else experiencing ringing or pounding in their ears? I am down to 5 mg from 25 mg and this began when I was at around 9 mg. It especially seems to come on at night when I lie down and sometimes it wakes me up. During the daytime it either lessens or else I don't notice it due to daytime other sounds.
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Thanks for your comments. Yes, it’s exactly why I’m taking it. I’m also on
Actemra infusions every 4 wks. The hope is that once I taper off Pred the
Actemra will take over completely. 🙏
@aflik
Do you have another condition besides PMR.? Several folks have mentioned being on actemra for PMR plus some other condition.., in my reading/research PMR is not one of the conditions for which Actemra is FDA approved! Just curious because my rheumatologist has not mentioned it!
Update: Parathyroidectomy 4 weeks ago did not solve the tinnitus. Still taking 5mg Prednisone for PMR. Hopefully as the dosage decreases it will subside.
I have tinnitus that comes and goes. Unsure what brings it on. Was tested by audiologist, mentioned it to RA doctor, and pharmacist to see if it is a side effect of Kevzara. No answers or diagnosis of cause.
Yes, I've had the ringing for a while now - I believe it started at 10mg (I was fine on the 20mg). I also have tingling and numbness in my fingers. I'm so over this PMR - I had two good days this week and today it's horrible. I look like an 80 year old walking around my work place.
@rebeccaheard I am now down to 4 mg and have permission from my rheumy to make my own decisions as to when to taper down, 1/2 mg at a time. He said a month at a time is fine with him. When I am getting ready to taper down I begin to alternate the old dose with the new dose so as to ease my system into the new adjustment. Thus far what I have found is that I have what I call a general feeling of broken glass in my arms and legs for the next 3 to 4 days once I am on the new lower dose, and then it settles down and I pretty much have some peace and quiet for some weeks till I begin the next 1/2 mg. Now and then I do have traveling pain, that is, sometimes the back of my hands, my toes, my shoulders, my hips. Here and there and random. I understand this is typical. I feel at my best when I've had enough sleep and that also means a half hour nap after lunch as well. When I have a rugged night's sleep everything feels awful. I try and stay off Tylenol as best as I can. I find the best thing for me, is to have my programmable coffee pot make me coffee by the time I wake up and I sit in bed and have a good, hot, strong cup of French Roast before I get up. Somehow this really really helps with the early morning creakiness. Then I can get up and start breakfast OK. The pounding in my ears comes and goes and it's only at night when I put my head down. I just had a checkup from the Dr. and my heart is fine so I presume this must be either the prednisone or the fact that I am 83 and the ole ears are going on me, perish the thought. I hope you will be feeling better soon, you have my sympathies.
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