Concerned about the side effects of anastrozole

Posted by tinalove @tinalove, Jan 31, 2016

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.

@auntieoakley

I will be looking those up right away! 😂🤣😂

Jump to this post

Oh, and one other thing, in case anyone is looking for help with redness and itching after radiation - Josie Maran's argan oil saved me!!! It helped things heal up quickly and 100% alleviated the itching and soreness. Her products are a Godsend!!!

REPLY
@deechase

I get them randomly but find that fans and cooler temps do help quite a bit. When I was walking outside during the summer, I really, quite honestly, couldn't even tell when I was having a hot flash anymore because I was just so hot, LOL. One thing I have noticed that helps is not wearing socks. For some reason, my feet are like car radiators - if my feet are cool, I stay cooler. It's weird but it's the only thing that consistently helps. I also, wear light clothing. I'm a QVC nut, so I buy a lot of Susan Graver's liquid knit clothing and Renee Greenstein's como jersey clothing. That helps a ton!!!! It is rather life-changing.

Jump to this post

I will be looking those up right away! 😂🤣😂

REPLY
@auntieoakley

Knowing that you could have any of those effects early make you stop and think, don’t they. Oh my goodness, your post made me remember when I was first starting all of this and I would be doing something and the hot flash would come and stay and my poor husband was being frozen out. Lol. Fans and A/C everywhere, even in the winter. I will say they are better now when it is cool, but in the summer I just have to drink constantly because I sweat constantly in a hot flash.
Do you get one when you change from outside to inside, or when you lay down at night?

Jump to this post

I get them randomly but find that fans and cooler temps do help quite a bit. When I was walking outside during the summer, I really, quite honestly, couldn't even tell when I was having a hot flash anymore because I was just so hot, LOL. One thing I have noticed that helps is not wearing socks. For some reason, my feet are like car radiators - if my feet are cool, I stay cooler. It's weird but it's the only thing that consistently helps. I also, wear light clothing. I'm a QVC nut, so I buy a lot of Susan Graver's liquid knit clothing and Renee Greenstein's como jersey clothing. That helps a ton!!!! It is rather life-changing.

REPLY
@deechase

Thanks so much for the kudos. I have been exercising like crazy for the last 1 1/2 years and have lost 30 pounds and put on a good amount of muscle. This was all before my diagnosis, but I feel that being in better shape, at the age of 51, helped me tremendously to get through the surgery, radiation, and now, the anastrozole and (upcoming) Zometa portion of the treatment. The decision to take the meds was difficult because of all of the collateral damage - bone loss (I already have osteopenia) and increased cholesterol (mine is finally coming down and I would hate to see it go back up again), among other side effects that seem to wax and wane. Hot flashes are killer now - much more so than before. I am postmenopausal but have had hot flashes for the past five years that were mild. Now, they are super-intense. Yuck.

Anyway, I do my best to work out. I do 20 minutes of elliptical every morning at 5:00 a.m., followed by 45 minutes on my Total Gym, then 20-30 minutes of elliptical over lunch, followed by more after work to make sure I get in my 10,000 steps each day. I was walking for 45 minutes over my lunch each day over the summer, but now it's just too cold and windy for me to go outside for my walks. I feel great, actually, and hope that continues. I take a number of vitamin supplements and Thrive products, which I believe help a great deal. I also drink water all day long and a green tea concoction with apple juice and take protein supplement powder in a smoothie each morning after my workout. It's a lot of work but is now the norm for me, and I feel great about it!

Jump to this post

Knowing that you could have any of those effects early make you stop and think, don’t they. Oh my goodness, your post made me remember when I was first starting all of this and I would be doing something and the hot flash would come and stay and my poor husband was being frozen out. Lol. Fans and A/C everywhere, even in the winter. I will say they are better now when it is cool, but in the summer I just have to drink constantly because I sweat constantly in a hot flash.
Do you get one when you change from outside to inside, or when you lay down at night?

REPLY

Thanks so much for the kudos. I have been exercising like crazy for the last 1 1/2 years and have lost 30 pounds and put on a good amount of muscle. This was all before my diagnosis, but I feel that being in better shape, at the age of 51, helped me tremendously to get through the surgery, radiation, and now, the anastrozole and (upcoming) Zometa portion of the treatment. The decision to take the meds was difficult because of all of the collateral damage - bone loss (I already have osteopenia) and increased cholesterol (mine is finally coming down and I would hate to see it go back up again), among other side effects that seem to wax and wane. Hot flashes are killer now - much more so than before. I am postmenopausal but have had hot flashes for the past five years that were mild. Now, they are super-intense. Yuck.

Anyway, I do my best to work out. I do 20 minutes of elliptical every morning at 5:00 a.m., followed by 45 minutes on my Total Gym, then 20-30 minutes of elliptical over lunch, followed by more after work to make sure I get in my 10,000 steps each day. I was walking for 45 minutes over my lunch each day over the summer, but now it's just too cold and windy for me to go outside for my walks. I feel great, actually, and hope that continues. I take a number of vitamin supplements and Thrive products, which I believe help a great deal. I also drink water all day long and a green tea concoction with apple juice and take protein supplement powder in a smoothie each morning after my workout. It's a lot of work but is now the norm for me, and I feel great about it!

REPLY
@deechase

I was told to take the anastrozole right away in the morning. I just started it on 10/27/21. I had some side effects in the first few weeks, but most have subsided or, at least, settled down a bit. I have to say the decision to take this medication was more difficult than going through the lumpectomy and the proton beam radiation. It's terrifying. However, the thought of having recurrent breast cancer is more terrifying. I realize this is not a guarantee, but I'm trying to do all I can to do what I can to be my own best advocate.

Jump to this post

Like you, I was told to take it first thing in the morning, I definitely agree with the water, I would add at least 30 minutes of walking or equivalent exercise was really helpful for me.
Kudos for you for stepping up and doing all you can for your future. Can you say why the decision was so difficult for you?

REPLY
@mdr3

How to find this? But I just want to share something else I have discovered with both Tamoxifen and Arimidex of late. Some oncologists don't talk about these two very practical things: sufficient hydration every day (can be up to 64 oz) and time of day the med is taken. I have found these two things to matter

Jump to this post

What time if day did they/you say you took your pill. I agree with the water👍

REPLY

I was told to take the anastrozole right away in the morning. I just started it on 10/27/21. I had some side effects in the first few weeks, but most have subsided or, at least, settled down a bit. I have to say the decision to take this medication was more difficult than going through the lumpectomy and the proton beam radiation. It's terrifying. However, the thought of having recurrent breast cancer is more terrifying. I realize this is not a guarantee, but I'm trying to do all I can to do what I can to be my own best advocate.

REPLY

What time of day is best to take it?

REPLY
@mdr3

How to find this? But I just want to share something else I have discovered with both Tamoxifen and Arimidex of late. Some oncologists don't talk about these two very practical things: sufficient hydration every day (can be up to 64 oz) and time of day the med is taken. I have found these two things to matter

Jump to this post

Can you please share the time of day ? Thank you

REPLY
Please sign in or register to post a reply.