Reclast Infusions: Side-effects & Recovery time
I just had a reclast infusion last week and have had serious side effects. I had the worst flue like aching for 5 days then my lefty arm became full of inflammation in the wrist, elbow and shoulder which caused extreme pain and I lost the ability to straighten my elbow. Ultrasound showed huge amounts of fluid throughout the arm. The right arm is now starting to have the same symptoms. The pain is excruciating. Has anyone else experienced anything like this? Neither the ER doctor nor the Dr. who prescribed the procedure knew what to do to ease the symptoms. Both arms from fingertips to shoulder are swollen and neither elbow will straighten. Anyone else have adverse reactions to the reclast infusion? If yes, how long did it last?
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Will this help build bones? Is that the once a yr shot or ?
Sorry for the delayed answer … My Endo had me do the following: Urine Crosslinked N-Telopeptide, c-Terminal Collagen Crosslinks, Osteocalcin and Vitamin D. His comment was that the results “tell us that the Reclast was effective in decreasing bone turnover”. I’ll do a Dexa in either 1 1/2 or 2 years (after that first infusion date) and see if my numbers are holding (and the markers are still good) and decide then if another infusion is needed then, or monitor and wait awhile.
Thanks for this! How long after your infusion did your endo conduct these tests?
The eye side effects worry me also. I have a chronic and severe dry eye problem. I have a lot of eye discomfort most of the time and do not need new inflammatory conditions. (another reason why I am reluctant to switch from Prolia).
Hi thank you for your detailed information regarding Reclast. I will be going for my 3rd infusion tomorrow and my bone density has increased. I don’t look forward to it. I usually feel like I am getting the flu, aches, feverish etc.. but I do exactly what you said drink water, I take Tylenol before and after. I am 69 now, also in good physical condition but it’s genetic and as you said: you do not want fragile bones . I was treated early 60’s but could not tolerate pills. So this is working so have to stick with it!
And yes, medications all have side effects, but so does OP and fractures!
Hope that helps someone too!
@sarai14 Thank you for the upbeat post! I’m supposed to start Reclast, just not sure when.
Sorry for my delayed response! I think it was about three months after the infusion .
Hello
I was wondering if anyone knew which drug has more side effects prolia or reclast?
I started on Prolia last June and was very reluctant after not tolerating Fosamax with side effects. So far I haven’t had any side effects that I am aware of. I will get my second Priolia injection in December. It is such a difficult decision! Judy
My endocrinologist did tell me that, when you stop Prolia to go on a drug holiday, there is a period of rapid bone loss and she suggested that I do the annual Reclast infusion instead. I had my first Reclast infusion in August.