Side effects from Zometa?

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CPB1167
CPB1167 Member Posts: 24

Hello,

Ive been taking letrozole for almost a year. My MO wants me to start Zometa infusions to prevent future osteoporosis. I am concerned about side effects, I am curious what anyone has experienced taking the Zometa.

Thanks so much.

Comments

  • JAS62
    JAS62 Member Posts: 3
    edited November 2019

    I've breezed through everything they've thrown at me, including no side effects from Arimidex, but Zometa has felled me. Even though I drank 160 ounces of water in the 24 hours after the infusion (and at least 50 ounces a day since then), I spent a week with strong flu-like symptoms (aches, chills, fever). Now in week 2, I'm severely lightheaded/dizzy and I can taste the salt in everything. A cheese pizza slice is nasty, for instance. I'm also exhausted, sleeping 12 hours a night with no problem.

    I've cancelled future infusions.

    On the other hand, my bone loss consists of 2/10s of a percent into osteopenia on one portion of my hip. I''ve got just one toe over the line into the warning track, and we haven't yet tried increasing calcium, weight training, etc. I'd much rather give that a try than automatically embrace something that screws up my life for 2 weeks+ twice a year. That would mean a month out of every year lost.

    And it's impossible to say how your system would handle this. You may feel slightly achy the next day and poof! You're up and about with no other symptoms. I think it's worth trying it to see, but have a Plan B if you don't like the outcome. Or have a much bigger goal than I do that makes the investment worth it.

  • AnnC2019
    AnnC2019 Member Posts: 203
    edited November 2019

    I felt sick the day after my first infusion. After that I felt fine. I was supposed to go monthly but it was switched to twice a year.

  • Boston12
    Boston12 Member Posts: 22
    edited November 2019

    I'm going for my third infusion on Tuesday and have had no problems with Zometa. my thumbs are achy, but that could be from any of the various treatments I've had. Everyone reacts differently, but I have heard that the reaction to the first infusion is the worst and the following infusions are easier.

    I took a bad fall a few weeks ago and didn't break any bones. That makes it worth it for me.

  • Billb464
    Billb464 Member Posts: 62
    edited November 2019

    I had my 1st infusion at the end of June, no noticeable side effects, just a little more achy than normal and tired a few days after. My next one is in December. Good Luck, I think that everyone has different reactions, so hoping yours are minor:

  • Hopeful82014
    Hopeful82014 Member Posts: 3,480
    edited November 2019

    I was advised to take a pain reliever before the infusion and to hydrate well before/after. Following the first infusion I was fine for several hours and did my normal workout. That evening I felt a bit as though I was coming down with a cold - chilled and unmotivated. I went to bed a couple hours early with my heating pad, herbal tea and a good book and I was completely fine the next day. I've never had even so much as a headache with subsequent infusions.

    I've known women who've had a rough time and others for whom it was a complete nothing and I cant see that any of us are doing anything differently, which makes it impossible to predict how it will go for any given woman. I'd say it's worth a try, however.

  • SUPer52
    SUPer52 Member Posts: 122
    edited November 2019

    I have my second infusion coming up in a few weeks. My first one went fine. About 24 hours after the infusion, I felt some mild flu-like symptoms, but by the next day I was back to normal.

    I am wondering if anyone on the 6 month cycle had any infusions less than 6 months apart. Somehow, when I scheduled my second infusion, it ended up being scheduled for more like 5 months and 4 days later rather than 6 months. I travel out of town, and I think they were trying to save me a trip and scheduled it based on availability of appointments with my MO so that I could just make one trip rather than one for the oncologist appointment and another separate one for the infusion. I called my oncologist's office to inquire whether that is too soon, and the nurse or assistant (not sure what her title is...) left a message that I would be just under three weeks early and that that would be fine. However, she is miscounting. My last infusion was June 28, and this one is scheduled for December 2. That is 5 months and 4 days, so 26 days earlier, closer to being just under 4 weeks early. Am I being paranoid about having this infusion too soon? I know we are all worried about the rare, yet severe, side effects, so I don't want to do anything to increase the likelihood that I end up being one of the unlucky few with ONJ or fractured femurs, etc. down the road.

    I would appreciate hearing from anyone in a similar situation. My infusions are given only to prevent the development of osteoporosis while on the AI since my DXA scan showed osteopenia in my spine and both hips. I am 52 years old. I know others receive it much more frequently due to metastatic cancer or other cancers, but mine is simply to prevent the osteoporosis. Anyone receive their infusions closer to 5 months apart rather than 6? Thanks and hugs to everyone!!

  • Hopeful82014
    Hopeful82014 Member Posts: 3,480
    edited November 2019

    I've occasionally had one scheduled at 5+ months, rather than six, with no ill effects. I wouldn't stress over it. However, if you’re deeply concerned it’s always your right to pick up the phone and reschedule the infusion.

  • SUPer52
    SUPer52 Member Posts: 122
    edited November 2019

    Thank you, Hopeful! I appreciate your response!

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