Does anyone have a solution to help manage Reclast side effects?
Does anyone have a solution to combat Reclast side effects. I had the infusion a year and a half ago and the side effects started shortly after I had the infusion. I still have weak legs, swelling in feet, pain in bones, dizziness (serious dizziness), cold sweats, tired all the time and nervous twitching in bones. Any suggestions?
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I am still having back pain and muscle aches 10 weeks later. I have not tried steroids but think they may help. I feel our bodies had an autoimmune reaction to reclasp. I think they use steroids for autoimmune reaction.
The medrall pack is only 5 days of steroids
Sometimes the five days of steroid can interrupt an immune reaction as they can become self-sustaining. I have heard that IV steroids are more effective with the Reclast reaction.
I had my reclast infusion July 24 of this year… as I’m texting this I’m in the Er because I’m in so much pain in my shoulders hip knees back and ribs… I can’t lift my arm over half way without it being excruciating painful..
I don’t know what they will or can do for me here but I’m at least going to have them check everything
I did the steroid pack for 5 days it didn’t touch it..
Everyone needs to be so aware of this terrible side effects!
Please! Research thoroughly before you go ahead! FDA should be stepping up with All the potential side effect
Will do, thanks.
@chuckster1957 Perhaps it would be helpful for you to know about a positive experience. I had my first Reclast infusion in May 2025 and have had no side effects whatsoever thus far. The infusion team at the center I go to told me that they rarely receive reports about severe side effects from their patients. As always with these medications, you just never know how your body will react. Wishing you all the best moving forward!
annms01, if you are still in the ER ask if they can give you IV steroids. I've heard that they are much more effect with Reclast side effects than the oral 5 day.
I'm sorry you are suffering.
Thank you for your suggestion.. after finding no rhyme or reason to my pain.. saying it was probably a mix of a flare up and the reclast..
I asked them for steroids in my IV but they said since I had just been on the pack a week ago they were hesitant to give it!
I’m suppose to call my RA Dr and go in so she can visible see I can’t move … it’s just frustrating..
I would have loved the steroid in my IV .. what do I have to lose at this point!
Thank you, for your suggestion I might suggest it to my RA !
I pray you are doing well ..
the journey continues!
Thank you for posting your positive experience.. I agree patients should hear those as well.. the ones of us that are experiencing the worst of course are here trying to find answers.. which I hear effects only 1-2% of patients!
Important to hand an open conversation of all side effects, even the low percentage, you could be I. That category!
I’m so glad it was successful for you .. thank you for your comment … I need to be more positive seems I’m pretty negative at this point because of my pain..so thank you for sharing the positive thoughts!!! Hugs to you!!