Concerned about the side effects of anastrozole
I completed all treatments for breast cancer but now I am supposed to take hormone blocker, named anastrozole. im concerned about the side effects. Has anyone here taken it and did anyone have hair loss?
Interested in more discussions like this? Go to the Breast Cancer Support Group.
CORRECTION!!! mY BREAST CANCER WAS DISCOVERED IN SUMMER OF 2016, NOT 2017. TIME FLIES!!
I have been taking Anastrozole for three years. I have ongoing, constant hot flashes and have recently noticed that my hair is thinning out and I have a couple of bald patches. The only thing that makes me feel grateful is that i am only dealing with those two side effects. I've had three colds this winter because even though I go out bundled up when it's cold out, I still sweat a lot. Just horrible. I think that next winter I should wear a surgical mask every time that I go out in the cold.
Hope this works better for you. Don't think I mentioned my hair, which was always thin, is now much thinner than ever - but I guess that should be the least of my worries!
I started on Anastrozole inFeb of last year - by Sept was having quite a bit of joint/bone pain. After a test that showed osteoporosis had increased in the last 3 years (breast cancer just discovered in 2017), the Dr. changed my RX to Exemastane in Dec. & started a twice yearly injection of Prolia, which I understand is supposed to help with bone thinning. Also, my hair has come back much thinner since the chemo -( don't expect that to get any better). The joint pain is still there & think it always will be. But - don't want the cancer to come back, either, so will continue with the meds.
I've been pretty lucky without the unpleasant side effects that some people have. But my DEXA scan after a year on anastrozole showed some incremental bone thinning. In spite of what the DEXA scans say, my bones aren't fragile - if they were, I would have broken something by now - but I'm seeing the naturopath at our cancer center and she has me taking a supplement called Osteo K, which is a lot more expensive than the anastrozole. I'll try taking it for a year and see if it helps. I may be having some hair thinning, and have added a few pounds that I'll blame on the drug. But mostly I'm able to stay active.
I have just been prescribed this medicine. I understand one of the side effects can be bone loss. Just wondered what other people are doing or using to help with this problem.
Welcome to Connect, @bmerxbauer. Have you experience bone loss with anastrozole?
I’m hanging in there, but continue to be challenged. Having taken Anastrozole and Aromasin— each fir 6 months, I stopped all for now 3 weeks, trying to regain “normalcy” with my hands & wrists. While slightly improved, like you, I’m not sure that’s achievable.
I’m starting letrezole/femara next week - my last option because tamoxifen isn’t an option for me. I am hopeful that the side effects are less problematic, given the desire to continue the meds for 4 more years.
Let’s keep talking.
I'm wondering how you're doing nearly a year later - I've switched to Exemastane due to the joint pain (elbow & wrists) and general bone aches. The aching has stopped but the joint damage/pain seems permanent. As I understand it, the side effects are very similar with the two drugs.
I started Anastrozole last Feb and switched to Exemestane in Dec due to joint pain. I still have the pain in my elbow and both wrists - maybe arthritis was always there and these have made it worse (I'm 75). I don't know what my estrogen levels are but am on Prolia every 6 months due to bone thinning. I guess it's just a matter of what helps one problem may make another worse.Also, my hair was always thin but now it's REALLY thin and that seems to go along with it all.