Stopping Anastrozole

Going through breast cancer treatment Hormone therapy
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Hi,

I have posted this on another part of the forum but now realised that this is a more appropriate section.

 

I am interested to hear from anyone who has stopped taking Anastrozole. I have stopped after 3 months. I have been experiencing various symptoms including depression, incredible tiredness and weakness, poor apetite and others. My consultant has agreed that these are possibly due to the Anastrozole and recommended that I stop taking for a while.

Has anyone stopped taking Anastrozole after similar symptoms? Did the symptoms improve and if so, how long did it take for you to see some improvement.

Thank you for reading and responding

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Hi Julie,

 

i too have stopped taking Anastrozole after 3 months on the advice of my oncologist at my follow up appointment after finishing rads.  My symptoms were hot flushes/sweats continuing  ALL night, aches and pains and feeling generally unwell.  He said that my body was unable to take it and advised I stop.  I spoke to a BCN  who who was  Not happy about me stopping completely but suggested I stop for 6 weeks to give my body a chance to recover and see how I felt.  I’m now 3 weeks into not taking it, aches and pains improved slightly, don’t feel quite so “sicky” but still hot flushing all night.  However, the sweats are much better and i am dropping off to sleep inbetween the flushes which I wasn’t while taking it.  I guess the flushes must be the menopause as I came off hrt the same time as starting Anastrozole.  Still got another 3 weeks to go to see if flushes and aches and improve and decide whether to give it another go or take my chances off it.

 

 

Good luck and keep us informed of how you get on xx

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Hi ladies it’s not quite the same, but I was having terrible joint pains on tamoxifen.  When I went on holiday, I was told to stop the tamoxifen a week before flying (T can cause clots & strokes), so ended up off it for 2 glorious weeks.  I had miles more energy & all the pains went away.  I reluctantly restarted it the day I got back & the joint pain hasn’t come back.  I am just telling you that because taking a break might have the same effect for you. x

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Thanks Bibi, that’s good to know.  5 weeks off Anastrozole now, still achey and still flushing at night but sleeping in between them.  Still not decided whether to go back on it next week after the 6 week break.  Maybe like you, having a break from it will help and I’ll give it another go xx

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Hi Julie,I also stopped taking Anastrozole after only six tablets. I couldn’t sleep, felt awful in myself and my joints were so painful. I couldn’t walk as the pain in my knees was terrific. I rang Breast Care Nurses who spoke to consultant. I was told to stop taking it and was put on Tamoxifen.
Well I was taken off that too after 11days, this time joint and muscle pain all over my body, migraines, moody, emotional, hot flushes and not being able to sleep due to the constant aches and pains. My Oncologist took me off it and after two weeks I felt myself again. He was hoping that having a rest from it I would be able to go on it again, so my new start date was when I had my first radiotherapy, I’ve now taken two tablets my joints are starting to pain me and I can feel myself becoming moody.
I don’t think my body likes these drugs!!
Hope you are starting to feel better.
Good luck Chris. Xx

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Julie…I see that you posted about a month ago. I stopped taking Anastrozole just over a week ago because of the severe joint pain and cramping in my hands and feet. I am hoping that my symptoms will diminish soon. Im wondering how you are doing with your symptoms after being off the drug for over a month.

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Just wondered if any of you tried acupuncture /reiki/ massage for your side effects before stopping treatment?

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I have not, but it is certainly something to consider. I just know that I can’t live with symptoms like I have been having. Quality of life is very important to me. I can deal with moderate side effects, but when they start to interfere with my daily activities something has to change. Thank you for the suggestion. I will look into it.

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I’m having 6 sessions of Auricular acupuncture courtesy of our local cancer charity. I think the auricular bit is the most important. It has made a huge difference to the frequency and intensity of the flushes and flashes and also has reduced anxiety and improved mood. I was a little sceptical at first but we have it as a group and all are feeling positive effects at different levels. It’s made a huge difference to me.

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I’ve been suffering terribly with a dry salty mouth…it was bad during chemo but has got progressively worse…mouth tastes of salt and it’s weakening and damaging my teeth.finally went to the doctor today who gave me a spray to try but is thinking it might be the anastroxole.I certainly don’t want to live with this as it effects every day of my life but wondering if any hormone blocker doesn’t do this?

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I don’t understand the necessity of anastrozole or any other hormone affecting drug for those of us who;
are past the menopause
have had our cancer removed
are not taking HRT
have had radio/chemotherapy
are having annual mamograms
I accept our bodies make hormones to some degree, but less so, and decreasing, which is why the menopause is so awful. But do we really need to take something that affects our body so extremely? We’re putting this stuff into us and our bodies are crying out in distress - is it really absolutely necessary???

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Hi. Just adding another two penneth from me!
I have come off Anastrazole after 6 months, so I can start Exmestane in a few weeks. I was struggling with joint pain, although my body had adjusted to the other side effects. I will keep taking the tablets, as this is my second hormone driven primary. I had a total hysterectomy almost 6 years ago and was told that should help prevent BC. Unfortunately it didn’t. Whilst there is a possible genetic cause, I really thought I’d be protected against Breast Cancer and I wasn’t. The first op gave me immediate menopause and these bloomin tablets the second! I genuinely thought I couldn’t have any hormones left in me post menopause!
Xx

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Hi. I am now 2 months into Exmestane and other than a couple of weeks where I felt rotten, it has had far less side effects than Anastrazole. My risk on NHS predict was too high not to take something, although I was seriously thinking I’d give up because of anastrazole. It only took a newly found lump (luckily nothing horrible) to realise I will continue. I have fatigue still but no achy joints. X

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Hello Jullue,
I am stopping it right now after my hair start falling . I was taking it for about 10 months , and really hated it! Thanks ! I will keep asking around

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I had that too/ I aged tremendously for s few months

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Really! Do we need that? I hate the way my doktor doesn’t even bother to engage in convincing conversation! I am stopping it after 10 months and wonder what withdrawal symptoms will have?

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I just stopped that medicine and I agree with you- 100pct . How did you stopped it? At once or using a scheme? My doctor was - let us wait see what happens in 3-4 months ? Why? And the start taking tamoxifen. No way

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I have been taking anastrozole for 4 1/2 years.  6 months ago I was diagnosed with high blood pressure…actually off the charts 200/120.  I’m a runner and have maintained my weight since starting this drug. My doctor could not find a drug regime that touched my BP. After a stay in the hospital and connecting with the caridology team in my town…my BP is under control with 3 different meds. I had my 6 month follow up visit with my oncologist this week and she informed me that I can stop anastrozole in 6 months and that it most likely has caused my high blood pressure. I’m in shock. I’ve been through the ringer the past 6 months trying to address these BP issues. I’m so tempted to stop this drug now. Has anyone else out there had BP issues?

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Hi Julie,

I’ve been on anastrozole since December, 2017.  At first I felt just fine.  After about a month, I got a return of terrible hot flashes, insomnia, anxiety, headaches, followed by bone pain - heels, thumbs, neck.  I was ready to go in and ask to change to another hormone blocking Med, but did a little research.  I started here, on this website, in a forum about side effects.  Then, I looked up research on side-effects of anastrazole, and how hot flashes should be treated in women with breast cancer.

 

Women with pain, insomnia, etc. tend to have more severe hot flashes.  This adds to fatigue and brain mush.  I thought that, if I could sleep, I would feel better.  I was feeling so bad, I had to quit my job, which I loved!

 

I ended up asking to be started on a new (to me) Medicine for hot flashes.  I was already on 75 mg of the extended release formulation of Effexor daily.  I switched my Anastrazole to the morning, to decrease the insomnia a little, and went to the next Medicine on the algorhythm for hot flashes - oxybutinin.  It’s supposed to relax your bladder, to make it hold more urine, and it’s used in small doses- 2.5 mg twice a day.  It is really strange to me, but I was better by the next day!  I slept a few hours for the first time in months, and I actually had my energy back!  I didn’t sleep as well last night, but I’m still better today.  The amazing thing is that my headache is gone, my bone pain is very mild, and my energy is back- all from treating the hot flashes! I had to share this, because there is hope, and I was hopeless 2 days ago!

 

i don’t know if stopping the anastrozole will help much.  I think it builds up in your system, and has ongoing effects, but I’m not sure.  Ask your doc to address your hot flashes, if you have them, and the Lord May help you as much as He helped me.  God bless you!  Braindoc

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Hi, I am new to the forum. I had a mastectomy in February, then told I must take Anastrozole for 10 years. I didn’t like the details of the side effects and at first thought I might not bother to take it. But when I read the research I realised it is really effective at reducing the risk of recurrence. I also found out that in early trials some women were given 0.5mg Anastrozole and that seemed to produce a significant reduction in oestrogen too.

So I decided to start Anastrozole by taking one every other day. I did ask my oncologist about taking half doses but she politely told me that wasn’t on. I have been in this regime for about a month. I had my oestrogen levels tested privately and the result came back as less that 18.4 pmol/L which is very low. (18.4 is the lowest level the test can detect)

i haven’t had any side effects on one every other day and I might stay on that level or go up a bit but I will have a blood test every now and then.

I know a lot of women give up Anastrozole because of the side effects, but that increases the risk of recurrence because your oestrogen levels rise again. Why not just go down to one every other day rather than stopping entirely. At least that way your oestrogen levels will be lower and so will your risk of recurrence. Anastrozole is effective and if you can stick with it all well and goid but in my opinion it would be a mistake to give it up entirely.

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