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.
My doctor told me to take Rogaine - You have to take it for like 3 months to see if it will even work. I bought some but have not used it yet.
I took Anastrozole for 5 years. I stopped 2 months ago, and I am still loosing hair. I have thick hair, but it is becoming more noticeable especially in the crown of my head. I am wondering when or if it will stop as well. Does anyone have any input?
Faslodex. Sorry about that
@dianamiracle, wow it looks like auto-correct made some interesting changes to some of the words in your text.
stomp tase inhibitors, obvious was supposed to be aromatase inhibitors, but "galoshes?" Is that supposed to be goserelin (Zoladex) perhaps? Or a new Minnesota winter phenomenon? 😉
I’m glad that you had another option. Wishing you the very best.
I could not take any stomp tase inhibitors. The pain and side effects were too intense and I was too close to going to the er. Mayo recommended galoshes, which is a monthly injection - one shot in each buttock. The only side effect is the day I receive the shot I am very fatigued and sleep in the afternoon. My body seems to be doing well on this. It is different for everyone, but worth asking about
@kathyomaha55
Kathy - I don't know if this will help. A cousin is on anastrozole and purchased some sort of "copper" gloves that she wears at bedtime and says that helps with the hand pain. I never tried that while on anastrozole because my heels, elbows, hands, spine, etc., were so greatly affected so I went off that as well as having horrendous headaches. I next tried letrozole - no headaches but the bone pain was bad. Have been on exemestane now for 3 months and can say it is not so bad, just some bone aches although not like with the other two types of pills and manageable - when it gets too bad then I take some ibuprofen. I was taking the pill at night to avoid any side effects but wound up with insomnia and now that I have switched to taking in the morning, not really having that problem. I do have some hot flashes, but they are not too bad - I just try to dress in layers and that works for me.
I just started Exemestane like 6 weeks ago. What were the side effects you had - if you don't mind me asking. I was on Anastrozole previously like for 11 months. My hands hurt so much it was unbearable.
Hi Trixie, I've posted several times about my bad experience with Anastrozole. I then went on Exemestane and had some negative side effects. Currently I'm taking a break from all the AIs and am scheduled to start Tamoxifen in January. I'm 75 and I'm very worried about blood clots with that drug, though. Does anyone have experience with Tamoxifen or have any credible information about the possible side effects?
I hope you see a difference. I was on Leterzole and had same problem. I even had a cognitive test, I though maybe I had start of dementia. Been off for 2 weeks and huge improvement. I start this weekend on exemestane, hoping do not have same problem.
Everyone reacts differently to AI, I have had no joint pain, but the fatigue and cognitive issues caused me problems. See discussion topic on Chemo Brain for more info: https://connect.mayoclinic.org/discussion/cancer-related-brain-fog/
Laurie