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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Welcome, @karenB76. Have you only recently started on exemestane and goserelin (Zoladex)? What is helping you to manage the side effects?
I pray you get some relief. It’s awful it really is. I never felt this way going thru menopause. I go back to my oncologist Friday so I’m hoping he starts me on something I can’t live with. I’ve had other ladies to ask about adjusting the milligrams or taking a day or two off if your dr approved it’s maybe you can check on that. Praying you get relief soon friend. I’m always here if you need to talk.
I agree. I’m struggling so bad. Joint pain. Hair loss. Hurt all over. Brain fog is horrible. Emotions. I don’t even recognize who I am anymore. They switched me to letrizole and I am not seeing much different at all. It’s horrible to have to just live this way.
Thank you for this idea. I will mention it to my oncologist. I’m willing to try anything.
@traci999 alternate days was immediately offered to me by my oncologist and is apparently quite common. I am still not sure why side effects would be better if it works to suppress estrogen, but my doc did suggest it. I stayed with the full dose but it was always an option to skip a day between pills.
I meet with my oncologist next Friday to discuss my options. I never thought of that so thanks I will ask.
Can you ask for a lower dose? The half life is 50 hours. Maybe every other c day?
I have been taking exemestane along with zoladex and I have fatigue, brain fog, and pretty severe joint pain. I'm not sure which drug is causing the side effects.
This comes up on this forum all the time and I ask every time: if the goal is reducing estradiol below detectable levels (and you may be well above that since testing stops at 5), what difference does dose make? if a 20% dose and a 100% dose both reduce estradiol below detectable levels, and the result is side effects from estrogen deprivation are the same, what difference does it make what dose we take? I actually asking the question. I don't see my oncologist anymore but if I did I would ask it.
ps great to have 100% estrogen score- the meds should work well according to what I have been told!
My oncologist told me I could take Femara alternate days. I never did, but that is one option. They tend not to suggest cutting pills due to inconsistency of dose and not sure if it is extended release. If not extended release, maybe your doc would let you do 1/2.
Some meds are weight-based and the company uses an average weight of, say, 150 (Evenity) and when dose does matter, that is a disservice to us small folks.
I’m ER 100% and PR 60%. I’m upset that women get the same dosage of medicine without blood work being done to 1) determine your baseline Estradiol level and 2) periodically check Estradiol levels after being on an AI. Seriously, isn’t monitoring numbers all about research? My Estradiol level is already the lowest in range at < 5, why should I take a full dose of any AI? Women need to question this theory. We are all different and should be treated like individuals … not treated with standard meds. That’s not fair to anyone.