arimidex side effects joint pain

I have had minimal obvious side effects, but some tough not so obvious side effects. It seems the longer I am on it, the side effects have been creeping in. I now have trigger thumb, hands are stiff. Had a bad fall in October, landing on my back and causing compression fractures in several vertebrae. I believe the anastrzole is complicating my recovery. Struggle with higher thought processes and memory issues. However, considering the alternatives.....the AI has not been so bad.

In the early breast cancer clinical trial, the most common side effects seen with ARIMIDEX include hot flashes, joint symptoms (including arthritis and arthralgia), weakness, mood changes, pain, back pain, sore throat, nausea and vomiting, rash, depression, high blood pressure, osteoporosis, fractures, swelling of arms/legs, insomnia, and headache. Patients taking ARIMIDEX were less likely than those taking tamoxifen to stop treatment because of side effects.

m not sure if it was just a mistake or if you intentionally made this a poll between Arimidex and its side effects, or breast cancer. If so, only your vote counts. You are the only one who can decide what is the best decision for you. I didn't see any question in your post, but if you do have one, we'd be glad to try to help.

I, too, have joint pain and swelling in hands (and sometimes feet) w/femara. I have developed a trigger finger and dequervains tendonitis in bilateral wrist w/thumb pain. Had to go off med for a month and also have sites injected w/cortisone. Never had any of this before. Oncologist said she had seen trigger finger before no dequervains tendonitis? Wondering if anyone out there has had any of these side effects? And what do you think of this? I am miserable w/all this discomfort.

the most common side effects seen with ARIMIDEX include hot flashes, joint symptoms, weakness, mood changes, pain, sore throat, nausea and vomiting, depression, high blood pressure, osteoporosis, swelling of arms/legs, and headache. Fractures (including fractures of the spine, hip, and wrist) occurred more frequently with ARIMIDEX than with tamoxifen (10% vs 7%). As for the burning...I,personally,have never been able to use anything but Ivory. Allergies.

Hi there, Thank you for writing to us here, though I am sorry that you are struggling with side effects from the result of breast cancer medication. I am also a breast cancer survivor, however as I am triple negative, the hormonal drugs are not effective for me so unfortunately I cant speak from experience. However, that doesn't mean that I cant find out some interesting information for you in relation to libido and Arimidex.

I have been on Anastrozole for year, 4 more to go (5 ys.) I have the worse Joint pain, stiffness, hurts to walk, get up from chair, I get out of bed hurting, I ache everyday. My skin and stays so dry, my hair grew back after chemo, but is lifeless, thin, etc. I do not like this Pill and want to discontinue, but my Oncologist said it is doing me more good, to keep taking it. This pill is really aging me, dry wrinkly skin, no energy, cant walk and move like I want to.

Since then I have had many of the typical side effects such as hand/joint pain, neuropathy in my hands, hot flashes, wakefulness at night etc. However, my sight in one eye has also begun to noticeably deteriorate. I know, because I had my eyes checked and a new eye prescription just before I started taking Arimidex. I saw my eye doctor again last week and my vision has deteriorated from 20/40 to 20/70 (with correction) in just a few months.

I hate to tell you but I am on Arimidex and I have joint pain in my hips and knees and my fingers are stiff and swollen -- It started two weeks after I started the Arimidex --- It may be gentler than Femara but for me it hasn't been a walk in the part either -- Sorry your mom is feeling so poorly -- I hope they help her quickly -- maybe she should be taking Calcium with Vitamin D in the meantime

Hi Japdip, Thanks for your reply. Yes, it was approved by my doc. The joint pain and hot flashes were much worse as well. I'm getting handfuls of hair every day in the bathtub drain. I am concerned that the hair loss is irreversible or may not grow back until I am finished with Arimidex. What I have read is the jury is still out if it's permanent or not, and I haven't read anything about going from one AI to another. I learned that Aromasin and Arimidex are quite different.

Oh well I guess I have no other option. Any thoughts? How bad are your side effects and do they disappear eventually?

As many of you know or have experienced, the AIs ( Arimidex, Femara, Aromasin), which are used to treat hormone-receptor positve breast cancer, often produce joint or muscle pain as a side effect. For about 20% of women, the side effects are so severe that they stop taking their medicine, which increases the risk that their breast cancer will recur.

I saw a Professor of Endocrinology in Feb 2008, referred by my bc surgeon, as this guy has an academic interest in side effects of Arimidex. He suggested I continue with Arimidex and Fosamax to prevent further bone loss, but I cannot stand the pain and disturbance to my sleep. Does anyone have any experience of stopping Arimidex and getting a different med that does not have the side effect of bone pain?

My side effects are joint stiffness, fatigue (which I think is because the Arimidex can keep you awake at night) and what I call a 'foggy brain". I also had my ovaries removed in Jan09 so it is hard to tell if the Arimidex causes the hot flushes or the surgical menopause. No depression or mood swings. All these things are more inconvenient than anything else. Whatever your doctor prescribes just try and if you find it intolerable, tell the doctor and try another.

Not to many effects in the first two months-of Arimidex- just a headache and some joint pain are my side effects. My surgeon ordered my Onco-I was a 17 with 8 percent rate of distant mets in 10 years low chance of recurrence for me. I will probably feel better when time passes as you say.. My doctors tell me I have a good prognosis. . Thank for the good thoughts - my life is different but I am just beginning to feel some safety in my thoughts of survival.

i. symptoms be a side effect of anastrozole (arimidex)? I have been taking it for 3 1/2 years, after 1 year on tamoxifen, following lumpectomy, chemo and radiation.

The plan is to switch to Arimidex-not sure exactly when-he originally said 4 weeks, but since I still have the joint pain, maybe we'll wait a little bit longer. I am wondering if this joint pain could be a side effect of the Lupron shots as well that I needed in order to start on the femara-anyone have any idea on that one?

Shortly after I started the drug, I started having hot flashes and bad leg cramps. My doctor then prescribed Effexor for those side effects. I started at 37.5 mg and worked up to 75mg which I took for 5 years. A month ago he changed my prescription to 37.5 mg and said to stop once the medicine ran out. I took my last pill 3 days ago. I feel horrible. I have nausea, dizziness, a swoshing feeling when I turn my head from side to side and just feel bad overall. I have been cranky and moody.

However after the chemo (4 cycles TC) I resumed the Arimidex and the joint pain has been much more marked. Joints affected for me are fingers, wrist, knees and feet and a general achy back when I'm too active. In general Ibuprofen relieves the worst of it but at age 60 I am feeling much older.

It is of course her decision re whether lowering the risk in her case is worth enduring the side effects. If she does choose to take an AI and the side effects of Arimidex are intolerable, she could see if she would do better on a different one. However, in at least one recent study, Arimidex came out ahead of the others in preventing recurrence. Best wishes to both you and your wife...

t believe you will see much hair growth. For further information on side effects from Arimidex the enclosed link is to an Arimidex Forum, check it: http://www.askapatient.com/viewrating.asp?drug=20541&name=arimidex Don't forget Arimidex is an Estrogen Inhibitor, that should give you a clue on what to expect. Take your time and read all you can from the enclosed forum link. Best regards.

Could it be your tamoxifen causing the joint pain? I took Arimidex for 6 months until joint pain started moving thoughout. Switched to Aromasin and the joint pain stopped. 18 month later now my hips are starting to hurt pretty regularily, will discuss with oncologist next visit. Basically blocking all the Estrogen is not a great thing for the joints.

However, in these small studies, they have found promising results in lessening the pain and bleeding episodes from endometriosis treated with arimidex. I would also just like to caution on the possible side effects of these drugs such as bone pains or fractures. Regards.

Arimidex side effects joint pain

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