arimidex joint pain relief

Is painfful intercourse a common side effect of Arimidex? I even have pain from just touching the vaginal area, plus burning from contact to various soaps except Ivory. Will this go away when I get off of Arimidex in 3 more years? My obgyn wants to give me estrogen cream but my oncologist is against it. What can I do to get relief? HELP!

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.

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.

I have gradually gained 40 pounds, continually have hot flashes and night sweats, have joint pain and now starting to retain water/have diarreah. I had a 135 IQ but after being on Arimidex lost the ability to do math and have problems with simple addition and subtraction. Also I have directional issues. I get lost easily, it being worse if I am overly tired or stressed out. I always keep a Garmin in my automobile. I also have acquired problems with spelling and remembering things.

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 have been on Arimidex for 4 months Femara first two months but the muscle pain was to severe. 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. .

2 months on tamoxifen, then Onc switched me to Arimidex in Feb 2004. I have had increasing debilitating severe pain in left hip, left foot and both hands. DEXA scan showed increased bone density loss to that of a DEXA scan done before bc (ordered by gastro due to 30+ yrs of steroids). BC surgeon prescribed Fosamax and Calcichew/Vit.D3. A bone scan showed osteo arthritis in both hips, hands and feet. No meds prescribed. I am on weekly injections of 12.5 mg methotrexate for Crohn's.

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.

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.

I tried first tamoxifen made me tired and nausous then I tried Femara, the pain was so great in my joints and muscle went off it I am now on Arimidex and 5 months into it it seems ok. I have gone off it once before one of my races because of pain. Arimidex is in the same family as femara only a little gentler..As my doctor said he doesn't know if it will help and it is not chemo but I am 16 months past chemo and have been on an estrogen blocker the whole time.

I went to a specialiast yesterday and the doc told me it may be beyond use for the rest of my life. I had an MRI today and will know the results in a couple days and yes they have done injections on area with little results so I will know in a couple days weather I will continue to have little use of the shoulder for rest of my life and thank you for your response.

ve found that none of these narcotic pain meds help much with the joint pain, not like they do with the nerve pain from the spinal damage. The NSAIDs that I took before I knew I had HCV helped a lot more with joint pain than the narcotics do. But that may just be me.

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.

I was diagnosed in 08 and am her2 positive. I went through chemo,radiation and 1 year of hercepton. Since then I"ve beem on arimidex. My main complaint other then hot flashes (terrible lol) is fatigue. It seems that I"ve lost alot of energy. The fatigue comes shortly after I start a project. Because of the hot flashes I get little sleep some nights but does the arimidex also cause fatigue? Is a side effect of hercepton fatigue (taken in 09,,,,?

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?

I have been to the doctor and am doing well. No cancer. One year later I have started with joint pain in my feet, knees , fingers, hips and arm and shoulder joints. When I sit I can hardly get up and going until it passes. In the morning it hurts in my feet and ankles to start walking but passes. Is this residuals from the chemo? This discussion is related to <a href='/posts/show/259132'>Residual joint pain after chemotherapy</a>.

If i work more than 8 hour or up for 8 hour , my leg starts hurting along with joint pain and nervousness and back pain. forgot I have high blood pressure now. what do i do. help please.

t be reached even for a biopsy to be taken the Arimidex cleared it by the next scan (6 months). I should point out that Arimidex was the only medication I was taking, no other treatment. The only reason my cancer has now returned is because a relief GP gave me the results of a bone scan and found that I had osteoporosis so she took me off it and by the time I saw my oncologist (another 6 months) the cancer had returned and metasized in my intestines and spine and ribs. Great fun!

For me when I was in acute withdrawal and had the most pain, I did get relief from brisk walks.. the relief didnt last, but helped for a bit. It was basically - 30 minute walk; 30 minute hot shower. Hot towels on the legs. I would wet a towl and microwave it for a minute to make it hot and steamy. I also tried using ben gay all over my legs and actually vicks too and wrapped my legs in a hot towel. (what a sight I was!).. the only true thing that makes it better is time. Hope this helps.

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 took Femara for a short time back last fall, and again this spring. Are any of you on Aromasin, Femara, Tamoxifen, or Arimidex experiencing joint/bone pain? If so, do you find it getting worse the longer you are on it? I finally got off IV chemo in favor of taking AI's because IV chemo was doing too much damage and I needed a break. My cancer is highly estrogen positive so AI's seem to be the choice for me at the moment.

Arimidex joint pain relief

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