← Return to Anastrozole experience: Any tips for managing side effects?

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@jayne1959

When I was diagnosed with Breast Cancer in April 2019, I had a Lumpectomy to my Left Breast and then 5 weeks of Radiation.
Then started on Femara which caused joint pain and my oncologist switched me to Arimidex.
I took it fatefully for 2 years and then I was having UTI’s one right after another and after I took medication for it. I mentioned this to my oncologist who laughed and said the Arimidex had nothing to do with it.
I decided to see if the UTI’s would stop after stopping the Arimidex and believe it or not, it did.
I did not appreciate my oncologist laughing at me for asking a question so I never started the Arimidex back and it’s been almost 3 years come July-August 2024.
I know the risks of it returning and some of the pathology reported Grade 2 & 3 and it read High Grade DCIS. My Ki-67 was 20.
Has anyone else had continuous UTI’s while taking Arimidex?

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Replies to "When I was diagnosed with Breast Cancer in April 2019, I had a Lumpectomy to my..."

I recently started arimidex - three weeks in, no real side effects. I am watching myself carefully and hoping for the best for you

This is good info from ACOG, American Congress of Obstetricians and Gynecologists:
“Why does estrogen loss cause UTIs? Estrogen helps tissues in your vagina and urethra stay elastic and moist. Estrogen loss can thin these tissues and cause dryness, irritation, and other changes that set the stage for UTIs.

For example, estrogen loss weakens the muscles of your urethra. This makes it easier for bacteria to enter your urethra and move up to your bladder.

Estrogen also raises the level of healthy bacteria that normally live in your vagina and bladder. Healthy bacteria help fight off infection-causing bacteria. After menopause, low estrogen means you have less healthy bacteria to help prevent infections.”

AIs leave us with no, or almost none, estrogen. It is very unfortunate when specialists only look at the top, highest frequency, side effects that are listed by the manufacturer.

Link to article:
https://www.acog.org/womens-health/experts-and-stories/the-latest/utis-after-menopause-why-theyre-common-and-what-to-do-about-them#:~:text=Why%20does%20estrogen%20loss%20cause,the%20muscles%20of%20your%20urethra.

I had read this as well and mentioned this to my Oncologist but he laughed and said it had nothing to do with it.
Thank you for your reply.

Did you use ARIMIDIX ( brand) or generics ? I had no UTI for 18 mos on generic but one since starting brand 2 mos ago. But the urine culture detected E. coli so I don’t think the medication was involved. All AI’s cause vaginal tissue thinning and drying so more susceptible to bacteria infiltration. I use a vaginal/vulvar moisturizer now.

I will continue to take the meds and I feel safer regarding possibility of recurrence.

Best to you.

I am so sorry to hear of your awful experience with your doctor. Having an oncologist who laughs at your side effects from Arimidex is unfeeling, infuriating and highly unprofessional. Never let a doctor make you feel like an idiot. You know your body better than anyone else. Many studies have shown that lack of estrogen can cause UTIs.
I had MANY side effects from anastrozole causing a very poor quality of life. My oncologist only acknowledged 2 of them, one of which was severe depression. She said they were pre-existing conditions and not caused by the aromatase inhibitor. Interestingly, all of my side effects, including the depression, went away after stopping anastrozole. Needless to say, I am now seeing an oncologist who does not deny known side effects. He also listens and responds with insight and compassion. Breast cancer has taught me to get a second opinion and never stay with a doctor who dismisses my concerns.
I wish you well. 💕

Thank you much.
Hopefully this will be my last year seeing this Oncologist.
If it reoccurs, I will be switching to an oncologist that has a professional and caring heart.

Thank you and I wish you the best in your health.

I was prescribed 10 mcg Estradiol vaginal insert tablet 2x weekly. This After my doctor saying, dryness is not usually a side effect (!)

My Oncologist does not take my concerns seriously.
After April of this year will be my 5 years since I was diagnosed with breast cancer and had my Lumpectomy and then I had 5 weeks of Radiation that started the middle of June 2019.
I see my Oncologist every 6 months.
I have my annual Mammogram on 2-28-24 and then see my Oncologist on 3-4-24.

Dosage of Anastrozole changed: One tablet every OTHER day. Why? Side effects from fatigue, depression, achiness, weakness, no energy to even take a walk. Went off pill Dec 13 to Dec 29 for family Christmas, back on Dec 30, then off again Jan 14. I was done with this S!?t!!!!
On Jan 30 went in for my 3rd round (every 3 mo) of mam/USound/consult. Lo and behold my left breast tumor was almost untraceable this time. It shrank big time. The right breast, the bigger tumor, was there but now splotchy and a little smaller. My surgeon, et al, were shocked at the difference. I was thrilled, but now, decision time? In talking I reminded my doctor what I had read (reliable source). There is a half-life of 50 hours for the drug. SOOO, I'm taking pill every other day. My dr. wouldn't go 3 days apart, but we both agreed on every other day. Going to see if I lose all my energy again.