Interested in side effects of Reclast Infusion

Posted by shrinkette @shrinkette, Jan 28 6:49am

I had a Reclast infusion one week ago and after some of the symptoms subsided, pain in my stomach continues. I have been taking Tylenol for relief and this all happens on the weekend of course and tough to get a hold of the doctor. Anyone else has this issue and what could be done besides the Tylenol?

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I don’t remember have stomach pain with my Reclast infusion, but my stomach has been over reactive to everything since I had COVID that it’s hard to tell.
Stomach ulcers are a side effect of Reclast in pill form. I guess it’s possible that what went into your system was strong enough to bother your stomach? Anyway, you might treat your symptom like an ulcer at least until you can get to the doctor. Food and drink choice would make a difference.

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@triciaot

I don’t remember have stomach pain with my Reclast infusion, but my stomach has been over reactive to everything since I had COVID that it’s hard to tell.
Stomach ulcers are a side effect of Reclast in pill form. I guess it’s possible that what went into your system was strong enough to bother your stomach? Anyway, you might treat your symptom like an ulcer at least until you can get to the doctor. Food and drink choice would make a difference.

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@triciaot
Thanks for your reply. I had an infusion one week ago. It’s the weekend and the doctor is not available. May be I’ll have an answer tomorrow.

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@shrinkette

@triciaot
Thanks for your reply. I had an infusion one week ago. It’s the weekend and the doctor is not available. May be I’ll have an answer tomorrow.

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@shrinkette, and all...I'm sorry you're having this reaction. Weekends are always fun, aren't they? That's when I get a UTI, or bronchitis, or pneumonia, or ????? No doctor is available...I had my 1st Reclast infusion last year but didn't have any stomach side effects as I recall. Possibly some intestinal issues as I frequently have that with meds.

My entire body reacted severely to this medication. I had the infusion on a Friday, which will not happen again. I live alone and the week-end was terrifying. After getting the infusion and about 8 hours of feeling fine at home, I began to have increasing all-encompassing pain throughout my body, every muscle, every joint, my head ached, nausea with no vomiting, I had a low-grade fever, sweats, and was hot to the touch, and had every kind of reaction...But, my tongue didn't swell, my throat didn't close or swell, my breathing was ok, no heart or chest pains, no hives or rash, etc., so after online research, I supposed I was not having an allergic reaction to the Reclast. My immune system was reacting to an unknown intruder...rather violently from my point of view.

At 3 a.m. Saturday, I called the Mayo Clinic Florida to speak with the on-call doctor in endocrinology. Yes, I made a conscious decision to wake up a doctor and ask questions to verify my conclusions. I was completely alone! I had no one to discuss or share any of what was happening, what I was experiencing, or to discuss my decisions and verify them for me. It was a great conversation, the doctor was very helpful and reassuring. She assured me my thoughts made sense, and that I was making the best choices. I suggested it wouldn't do any good to go to the ER for help. What would they do that I wasn't doing at home? She agreed. So, I took Tylenol, drank my filtered water, drank electrolyte water, and stayed in bed in a lot of pain no matter what position or how I lay there...It was a difficult, horrible week of pain I thought would never end, with moaning and tossing and groaning. But, I knew what was happening and why and accepted that it was ok. My body, whenever it came out of this fight mode, would be better for the medicine that would hopefully keep me alive a bit longer, and my bones from breaking increasing the chances of an earlier and painful death.

I hope this makes sense to some of you. It's taken a long time, and been a difficult journey to get to this place of acceptance in my thinking. But, it's a great place to be.

Interestingly, I had decided to have the 2nd Reclast infusion this year no question. Now, after the year I've had with 2 difficult and physically challenging colonoscopies, 2 bouts of Covid infection since July 2023, bronchitis, new diagnoses of PMR, GCA, and another very rare autoimmune disease, Covid pneumonia, and all the other stuff we all experience, I've decided my body is too fragile to go through the possible reaction to Reclast a 2nd time. So, I'll decline to have the 2nd infusion. I will also decline any more colonoscopies or any other invasive procedure that I don't think will lead me to a more pleasant, peaceful, and acceptable life for the rest of my life.

I am proactive. I have choices. I will decide what is best for my life. I think it was wise to have the Reclast last year. I think, in my situation, with my body fragility, it is best for me to not put myself through any more unnecessary discomfort or pain. Isn't this a wonderful place to be, mentally, emotionally, and spiritually? I love it! I'm grateful!

Blessings to all, Elizabeth

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Hi
I have had 2 infusions. My first infusion I felt flu like symptoms for 3 days after with a headache. My pharmacist advised me to drink Gatorade the day before 2 btls and 1 the morning of plus take tylenol the night prior and morning of. My 2nd infusion I had no side effects. I will be having my 3rd infusion this May. I did not have stomach issues as a side effect with either treatment..

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@sue417

Hi
I have had 2 infusions. My first infusion I felt flu like symptoms for 3 days after with a headache. My pharmacist advised me to drink Gatorade the day before 2 btls and 1 the morning of plus take tylenol the night prior and morning of. My 2nd infusion I had no side effects. I will be having my 3rd infusion this May. I did not have stomach issues as a side effect with either treatment..

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Sue417,
This is reassuring. I will probably start Reclast in June. Hoping my experience will be much like yours.

REPLY
@ess77

@shrinkette, and all...I'm sorry you're having this reaction. Weekends are always fun, aren't they? That's when I get a UTI, or bronchitis, or pneumonia, or ????? No doctor is available...I had my 1st Reclast infusion last year but didn't have any stomach side effects as I recall. Possibly some intestinal issues as I frequently have that with meds.

My entire body reacted severely to this medication. I had the infusion on a Friday, which will not happen again. I live alone and the week-end was terrifying. After getting the infusion and about 8 hours of feeling fine at home, I began to have increasing all-encompassing pain throughout my body, every muscle, every joint, my head ached, nausea with no vomiting, I had a low-grade fever, sweats, and was hot to the touch, and had every kind of reaction...But, my tongue didn't swell, my throat didn't close or swell, my breathing was ok, no heart or chest pains, no hives or rash, etc., so after online research, I supposed I was not having an allergic reaction to the Reclast. My immune system was reacting to an unknown intruder...rather violently from my point of view.

At 3 a.m. Saturday, I called the Mayo Clinic Florida to speak with the on-call doctor in endocrinology. Yes, I made a conscious decision to wake up a doctor and ask questions to verify my conclusions. I was completely alone! I had no one to discuss or share any of what was happening, what I was experiencing, or to discuss my decisions and verify them for me. It was a great conversation, the doctor was very helpful and reassuring. She assured me my thoughts made sense, and that I was making the best choices. I suggested it wouldn't do any good to go to the ER for help. What would they do that I wasn't doing at home? She agreed. So, I took Tylenol, drank my filtered water, drank electrolyte water, and stayed in bed in a lot of pain no matter what position or how I lay there...It was a difficult, horrible week of pain I thought would never end, with moaning and tossing and groaning. But, I knew what was happening and why and accepted that it was ok. My body, whenever it came out of this fight mode, would be better for the medicine that would hopefully keep me alive a bit longer, and my bones from breaking increasing the chances of an earlier and painful death.

I hope this makes sense to some of you. It's taken a long time, and been a difficult journey to get to this place of acceptance in my thinking. But, it's a great place to be.

Interestingly, I had decided to have the 2nd Reclast infusion this year no question. Now, after the year I've had with 2 difficult and physically challenging colonoscopies, 2 bouts of Covid infection since July 2023, bronchitis, new diagnoses of PMR, GCA, and another very rare autoimmune disease, Covid pneumonia, and all the other stuff we all experience, I've decided my body is too fragile to go through the possible reaction to Reclast a 2nd time. So, I'll decline to have the 2nd infusion. I will also decline any more colonoscopies or any other invasive procedure that I don't think will lead me to a more pleasant, peaceful, and acceptable life for the rest of my life.

I am proactive. I have choices. I will decide what is best for my life. I think it was wise to have the Reclast last year. I think, in my situation, with my body fragility, it is best for me to not put myself through any more unnecessary discomfort or pain. Isn't this a wonderful place to be, mentally, emotionally, and spiritually? I love it! I'm grateful!

Blessings to all, Elizabeth

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@es77
So sorry that you had to go through all this.
I totally feel for you and the pain you have to endure.
At his point, I’m not sure if the cramps that I’m experiencing are related to the Reclast infusion.
Still playing phone tag with my doctor.

REPLY
@sue417

Hi
I have had 2 infusions. My first infusion I felt flu like symptoms for 3 days after with a headache. My pharmacist advised me to drink Gatorade the day before 2 btls and 1 the morning of plus take tylenol the night prior and morning of. My 2nd infusion I had no side effects. I will be having my 3rd infusion this May. I did not have stomach issues as a side effect with either treatment..

Jump to this post

@sue417
Thanks for sharing your experience with Reclast. I somehow feel more reassured and think that my stomach cramps and the infusion may not be related.
Still playing phone tag with my doctor.

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Hi
Also, what was the time frame your reclast was given to you. My pharmacist told me to tell them to give it to me over 45 minutes. And that makes a huge difference, because usually they only give it to you over 15 minutes.

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@sue417

Hi
Also, what was the time frame your reclast was given to you. My pharmacist told me to tell them to give it to me over 45 minutes. And that makes a huge difference, because usually they only give it to you over 15 minutes.

Jump to this post

My infusion was about 25 min. I was there a total of 45 min - that might be why they are telling you that amount of time. It took about 15 min to get me settled into the chair, blanket, explanation of procedure, arranging tubes and holders. Then a few min to undo everything. I think they told me I could sit for a bit if I felt I needed to - but I was fine. I had no effects until about 6 hours later. 14 hours after infusion I was pretty achy. 30 hours, back to normal.

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Following this thread to see if any of my side effects have been experienced by others after my first Recast infusion. I did all the recommended-plenty of water day before and following and felt fine until about 10 hours after my infusion. I woke at midnight to pain in my upper back, ribs and sides-no where else. It was uncomfortable taking a deep breath but I wasn't short of breath. After finding a propped up position, I managed to sleep off and on until 6am. At that time I felt dizzy and my skin was hot-temp was 100. As I was a little dizzy, I checked my BP and it was low 90/60-totally unusual for me. Through the day I drank a lot of water and gatorade, took Tylenol and rested. By evening I felt better as far as the discomfort went but it took several days to feel almost back to normal. My BP did return to my normal and I reported these side effects to my Dr. so we could discuss before my next infusion. I had expected all over aches and flu like symptoms so this was a surprise for me. Anyone else?

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