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?
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Same here.. fingers crossed for both of us with the Exemestane!!
Like @rozv they finally switched me from anastrozole to exemestane, which I started 3 days ago. So far so good. We'll see in a couple of weeks...
Everyone's experience is different, and you may have no or minimal side effects. I was on Anastrozole for 6 mo's and developed severe joint pain, insomnia and some memory issues and hair thinning. I had a one month break and just started on Exemestane 2 days ago. The joint pain and insomnia resolved once I stopped the Anestrozole. I had taken Tamoxifen 16 yrs ago for my first DCIS and the joint pain with the Anestrozole was more severe., But the hair loss was worse on Tamoxifen. There were no other srmotsse inhibitors 16 yrs ago, so I am very glad there are other options to try if you have difficulty with what was initially recommended . Wishing you the best with your experience you have no or very mild issues.
I know it’s hard to be in a good mood and make everyone happy around you when you feel terrible. Hang in there take care of yourself. Be sad if you need to be. This is your moment. Other support you as you have supported them.🙏🏻
I can’t express the tremendous feeling of support from this site. While I try to keep a brave face for my husband, friends and family-I can share my honest feelings here. I don’t look forward to taking anastrozole for 9 more years and verzenio is really trying my patience to put it mildly. But! I will plug along until something better comes along. In the mean time, on rough days I will ask for support and on good days I will offer support.
@kathyomaha55 did not k ow that about cataract. Thank you. I took Anastrozole for 2 1/2 yrs so far the small start of cataracts has not progressed but I’ll keep an eye on them! Pun intended 😂
The AI drugs causes cataracts to grow faster. Be aware of this.
I agree it was really frustrating to not be allowed to get this test. It did not make any sense to me either. My original Oncologist had retired - so I filtered thru several replacements this last year. I wonder if I had the first one - who I really liked - if she would have explained more to me. I had Stage 1 IDC with no lymph node involvement. I got the Oncodx Type test & was a 22. So I could skip chemo but had lumpectomy & radiation. When the final doctor I saw told me that another 5 yrs would only reduce my reoccurrence by < 3% - it only confirmed my resolve to stop at 5 years. ONE other thing: Apparently all AI drugs (not sure if this includes Tamfoxin) - causes CATARACTS - makes the grow faster. After 5 years I now need cataract surgery as well. I'm 68.
I had Stage 1 IDC with no lymph node involvement. I got the Oncodx Type test & was a 22. So I could skip chemo but had lumpectomy & radiation. I also was given anastrozole first - after 6 months my hands, Shoulders and toes hurt so bad. I threatened to go off all meds if it was not switched. They sent me to a rheumatologist to eliminate my hand pain as arthritis. I was finally switched to exemestane and after about 2 or 3 months the joint pain faded. I don't know if she first prescribed the initial drug because of insurance. Good luck reaching the 5 year mark.
From what I understand, BC I test is given to patients with initial stage 1 to 3 cancer, and you have to fill a requirements form. I am in the same situation. After talking to my oncologist, I am stopping anastrozole now and switching to EXEMESTANE, which apparently is better tolerated. Why not prescribe EXEMESTANE to begin with then? Because of insurance.... They won't cover it unless Dr. says you can't tolerate anastrozole any longer... Unbelievable. Good luck to you. Stay positive. I really believe in the power of a strong and positive attitude.