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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Wow, you hang in there! I am stage 1A and 64 and could not stand the side effects! I tried it 3 different times and each time the effects worsened. I have more of a choice than you! I was told anywhere from 3-10 years to take. But again I am at 3-10% recurrence and my age and 4grandsons, I do not want to be a sedentary Grammy! Keep it up, Girl!
Hi. I started on Anastrozole in early October. By mid-November, my joint pain was so bad that I dreaded going from sites to standing position or having to squat down for any reason. My doctor put me on a “drug holiday” - not as fun as it sounds lol -where I did not take the drug for 3 weeks. I went back on the drug on Dec 11 and so far have had minimal side effects. My oncology team does not know why this works, but have found that often after taking a break from the drug, the side effects are lessened once back on. I am 47 years old and stage 3, so feel that not taking an AI is not an option for me. So, if your pain gets to the point that you feel you can’t endure be sure to talk with your medical team about the possible benefits of a drug holiday. It just might work for you, too! I’m also curious about the 10 yr expectation of you taking the drug as I was informed (and the little bit of research I’ve done seems to support) that there is no added benefit to 10 yrs vs 5 yrs of AI. If anyone has other info, I’d love to hear it. Thanks. And we are all so much stronger than we think we are! Hang in there, all!
Hi @ljwright4778,
I moved your posts to this discussion on Anastrozole (Arimidex) so that you could reconnect with the members who've joined this discussion. I’m so glad you’ve reached out to the Connect community with your questions, and I’m confident fellow members will join in and share their insights.
This sounds exceedingly familiar! I take the anastrazole in the evenings since I take Ibrance in the mornings. I have had severe hand and wrist pain as well as knee and hip pain. My doctor recommends Claritin to help with the joint pain. The other thing that has helped me tremendously is sunlight! We just returned from two weeks in Florida and I couldn't believe how much better my hands felt there. Best of luck as you navigate this adventure.
I have just started Arimadex and wanted to hear from others taking this drug. My Dr. said I will be taking this pill for the next 10 years. He stated that I will have joint pain in my hands and wrists. I experienced that immediately! I take it at night because I feel into a deep, deep sleep about 3 hours after taking it. I am a school teacher and really do not need to be falling asleep with students!
I feel depressed and unmotivated, my joints ache all the time. I am taking calcium with a Vit D supplement. My knee was hurting from laying on the radiation table and it hasn't gotten better. Here are my questions, does the joint ache go away with exercise? I used to play tennis and I still play the piano and I REALLY do not want to lose any of these activities. I am starting to get out on the courts but when I get home, my body is so sore, I can't move.
I am thinking about taking the pill part time but when I didn't take it for Christmas, it seemed like the joint pain was WORSE! So my questions are:
Do you take ibuprofen to help the achy joints or another supplement?
Do you find that taking the pill at night that you still are restless and mornings are very hard to get out of bed?
Does exercise help relieve the joint pain? I know it will help the bone loss!
What essential oils does anyone take to help with these side effects?
I know these questions are numerous and a little disjointed but this is what is on my mind! The pain in my body makes me feel like I am 80 and not 60, sad and not happy like I normal and have a very short fuse!
Thank for your input!
Weighing in (right smack dab in the middle of this)......I couldn't take the AI's........got all the side effects and then some. I have a 7% chance of recurrence and my oncologists (all 4 so far) finally agreed that I should just move on. It's a tough decision because you sure don't want cancer again but some of us can't tolerate the meds either. Hugs on the tough decision. I hope mine is right but I won't know for some time (if ever). p.s. I lost my hair anyway and I had great hair. Now I have spindly, sad hair but I've learned to let it go and embrace my winning personality. The changes, the decisions, the stress.........it's a triple whammy this cancer journey.
Did you lose your hair on letrolzole?
Yes, I am wondering if it will eventually go away or lessen. I also wonder how people are dealing with it. Do you take it at night or in the morning?
Omg, I took 2 times at 3 week periods...thought I was going to die! The second time I tried I could barely get out of bed anymore! I have fibromyalgia and thought that was painful...ha!
I could barely move my fingers. Needless to say after reading through all my paperwork and finding I am at a 3% chance of recurrence and due to quality of life I have chosen to take nothing! I have 4 grandsons and want to be able to get down on the floor and play with them not lay in bed for the next 5-10 years!
My oncologist is not happy but my primary and pharmacists say otherwise-they know me!
It is a tough call.
Blessings and hugs
@ellenveragilmor
My hair returned similarly, but that also may be because of my age. Many women's hair thins on top as they age and it likely was thinning before chemo. As to worsening arthritis and weight loss on anastrozol, I would encourage you to speak to your oncologist and ask if you can switch to another AI and see if that helps (there are several other choices). I also lost weight at first with anastrozole, and then my weight leveled-off after 8-9 months. I attributed the leveling-off to the initiation of a strenuous exercise program which helped me sleep better, eat more, and regain lost muscle mass.