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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I have been taking anastrazole for almost 5 years. I think my hair is thinner, but I’m not sure if that was the result of the hair loss from chemo, the fact that I have thin hair to begin with, and I’m older, or the Anastrozole. The bigger issue I’m having with the anastrozole is an almost total inability to lose weight. I don’t think I’ve gained any or if I have, I haven’t gained much, but any attempt to lose weight almost always fails. When I talked to the chemo doctor about it and explained that I was getting , for a 71-year-old woman, an extremely high amount of consistent exercise, was following a sensible diet, and still could not lose anything. His response was it is the Anastrozole. For some reason it causes fat cells to settle in adipose tissue rather than be burned off by activity.
I had no side effects on Anastrozole for the first year. Then I got dry eye and a huge stye, which was treated with moist heat and antibiotics. Now I feel like I have a UTI, which is a side effect but may not be related. Otherwise, nothing else. No hair loss. Does depression count?
How are you responding to tamoxifen?
OMG!! this is ME! Going through d same exact thing… don't know which way to go.… I'm like I don't want to take this med (Tamoxifen) it can cause uterus cancer and stroke, blood clot just a whole lots of stuff!
Check with your oncologist or pharmacist regarding “safety”. If it is just know that it’s a daily dose and can be stopped ( and replaced) quite easily if it’s not working out for you.
Best 🌸
I have just started to take Anastrozole after having lumpectomy & radiation for stage 2 ER+ breast cancer with clear lymph nodes.
I also have thalassemia minor & gilberts syndrom.
I’m quite anxious about taking Anastrozole as I’m not sure this is safe for me considering my health situation.
Thank you for your kind words!
@tamtam24 (((HUGS))). You are not alone. We are all here for you. I’m sorry you are going thru this. I took Anastrozole and had side effects. Took it for 2 1/2 years. Maybe ask your dr to prescribe a different AI or I’ve also hear others here say getting the name brand vs generic made a difference. Talk to your dr and try and get them to listen. Blessings & hugs.
I am crying as I write this because you capture perfectly how I feel on Anastrozole. I don't even recognize myself in the mirror - weight gain, thinning hair. Plus, I have raging insomnia that leaves me tired all the time. I find that oncologists, naturally, just care about the cancer returning and downplay the side effects. That then leaves one feeling so alone, like a failure if you experience side effects that they minimize.
Has anyone found any significant difference in hair thinning between the various inhibitors? I've been on Anastrozole for about a year and a half. I have knee pain/stiffness when I get up from a chair or walk up and down stairs, but once I get going on a flat surface, no pain. I also have chronic tiredness and terrible insomnia. However, I can live with all those. The hair thinning is particularly tough for me because I already struggled for years with androgenic alopecia. Fortunately, it was mostly around the hairline and on top and I have naturally wavy/curly hair, so even the dermatologist I saw a few years ago had to get right on top of me to notice. I then started taking Rogaine, which seemed to stabilize my hair. However, since being on the Anastrozole, the thinning seems much worse. I don't lose hair, just each hair is so thin. I've had two really humiliating experiences recently where I was in a picture and shocked at how noticeable my thinning has become. I know that the hormone therapy is key, but, boy, I already felt so bad about myself and how I looked, and now I feel so defeated and depressed. Any insights? Experiences? Advice? Thanks for listening!