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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@thornwood. I hope the pain is temporary and will improve very soon. Do you feel the pain is definitely from Reclast?
JK
I do. My doctor has given me a prescription for Motrin that has helped ease the pain. I still have dizziness and stomach issues. Did not have these problems before I took Reclast.
Thank you for posting. My endocrinologist recommended Reclast because my T score at spine is -4. I am very leery to have injection because I have nightly heartburn (while on medication) and read that heartburn is a side effect for this drug. I’m very apprehensive and would rather go the natural remedy route.
Good morning @giovi, welcome to Connect. Thank you for joining this discussion about choices for fighting and controlling osteoporosis. There are multiple directions to go. However, as you note, you have a special medical condition that needs to be considered before committing to an option.
We are all different and the newer daily injectable options appear to have one major opportunity......we can stop immediately if we run into a side effect problem. For those of us who are unable to tolerate bisphosphonates, we are just beginning to be able to measure results for the alternatives.
I am so encouraged to see responses and inquiries from Connect members. Our shared experiences are contributing to a helpful body of knowledge.
May you be safe and protected.
Chris
I will be posting my results of DEXA scan there in 4 weeks. I can't wait to see if I have improvement.
I was also troubled with nightly acid reflux. My doctor told me I was going to be in horrible trouble if I didn't get a handle on it. I found I was having problems with pepper and I needed to eat earlier and take digestive enzymes. The reflux seems to be under control now. But I do not use any drugs like Reclast. I am going the natural route. My DEXA scan score was -5.7. I'll be getting tested again in a month (April). I can barely wait to see if there is improvement. The fracturing stopped, so I think something is better.
@parrotqueen Cant wait to hear what you find out as my T score is 1.5 and am on the natural route . last August I did have another fracture so not lifting anymore . Have you researched the peanut oil ?
I have not done anything because I've had meningitis (it is a side effect of getting IVIG - supposed to be rare, but I've had it four times now). Also, I am preparing to hunker down for Corvid 19 as I don't have an immune system and I'm 69. There are a lot of cases of it in my county. Thank goodness I started preparing early - you can't buy Purell, a mask or anything. I have a box of masks because we live in a wildfire area, but I can only find one. I got some inexpensive disposable surgical masks to wear to remind me not to touch my mouth or nose when I am out and about; seriously, we are all so used to doing it, we aren't even aware we are doing it. If you have a mask on, you are protected from yourself.
You know things are bad when at the end of the hour your therapist says "I'll see you next week if we are so lucky to still be here."
Thank you. I joined the group.
Thank you, Chris. I am going to ask my PCP about natural remedies at my next visit instead of Prolia, Forteo, Tymlos etc. The list of possible side effects is frightening. Many of my friends who have taken Fosamax or Prolia no longer take it because they developed heartburn. I feel like I am in a Catch22. The acid reflux drugs are bone thinning but I haven't been able to discontinue them.