how arimidex works

I am thinking of adding a supplement with the arimidex (broccoli seed extract - a natural aromatase inhibitor) and monitoring estradiol/estrone with blood tests after starting the supplement. If there were a negative interaction between the arimidex and the broccoli seed extract, how accurate would the blood test's estrogen results be?

Yup, joint pain is a very common complaint with aromatase inhibitors. I'm taking Arimidex and commiserate with Rusty, in fact that's how if feel in the morning ... rusty! I was on Arimidex for 6 weeks when I found out I needed chemo. The joint pain was very minimal and I already had some osteoarthritis. However after the chemo (4 cycles TC) I resumed the Arimidex and the joint pain has been much more marked.

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!

Expander could not be put back in so 1 breast has expander and the other nothing. I will have reconstructive surgery April 2014. I started arimidex December 2013 I have experienced hot flashes which I'm used too. I take a organic bone support supplement. I've been in physical therapy since October 2013 which has helped me tremendously. Now after two months on Arimidex I am experiencing vaginal dryness that is quickly getting worse.

My Son has bone age of 14.6 and just started arimidex to delay growth plate fusion. How long can arimidex delay fusion?

So you are not taking Tamoxifen at all ? How long do you have to be on Arimidex ? Isn't 5 years too long with all the side-effects ? Do you take any calcium or vitamins ? Thanks for your answer, Have a nice day.

It works to keep the cancer at bay. 20% of the people with my type of cancer make it past 2 years and I am going on 7. Unfortunately the side effects are now too much witht he water retention. I have made myself exercise a min of 3 times a week and truly believe it has helped with the side effects up until now.

I learned that some weman experienced elevated blood pressure and blood clots while on Arimidex. And Arimidex is known to cause high blood pressure and blood clots. How do know for sure that Arimidex is the cause of my high blood pressure?

I just completed 5 years on arimidex and have been asked to be part of a study and go on it for another 5 years. Has cancer reoccurred in patients while they have been on arimidex, not due to the drug, but due to the cancer. In other words, does taking arimidex prevent cancer from reoccurring while a patient is on it?

Does Arimidex have to actually kill you vs. maiming you for life, in order to be pulled off the market? At 58, I may need a hip replacement because I took Arimidex for two years! DeeDee This discussion is related to <a href='http://www.medhelp.org/posts/show/260593'>Arimidex Long Term Side Effects</a>.

Well, for me Arimidex was so very horrible, I barely lasted three days on it. I was in an almost catatonic state of depression two hours after I took the first dose, and then got just about every other bad side effect soon after. Femara, in comparison, relative to the other, was not so bad at all and I lasted almost thirty days. But not every woman has the same problems, or any at all. Many though do have some problems.

I would advise you to have a serious discussion with your Oncologist regarding the problems you are having with the Arimidex. There may be another medication that you could switch to that wouldn't cause so much pain and destruction. You might even have to weigh the benefits vs. these severe side effects and have to discontinue the drug on the basis of the findings.

Dear madwilson, Hairloss is not a usual side effect associated with Arimidex. Arimidex is an aromatase inhibitor. This means it blocks the enzyme aromatase (found in the body's muscle, skin, breast and fat), which is used to convert androgens (hormones produced by the adrenal glands) into estrogen. In the absence of estrogen, tumors dependent on this hormone for growth will shrink. For more information regarding this drug and side effects you can check out the website chemocare.com.

When I say that I tried Arimidex, Tamoxifin, and Femera..... Arimidex made my joints so stiff and sore that I couldn't even walk without extreme pain. So I was put on Tamoxifin and within 3 months my WBC dropped to 1.3 which is one of the rare side effects. At that time I was changed to Femera, shortly after that I had vaginal bleeding so they did a D/C and 2 weeks later I started bleeding again.

Please inform me of side effects of Arimidex. Also confirm whether clinical tests proved that arimidex really prevent cancer from returning. Recently I had a lumpectomy. The cancer was confined to the lump in my breast and did not spread to the limph nodes. I had a serie of 30 radiation treatments. My bone density is deteriorating, thus I would like to know whether I have to take osteobond 70mg weekly. Will arimidex contribute to loss of bone density? Thank you very much. Susan.

I switched to Aromasin from Arimidex and my I began losing my hair immediately. Changed back after 6 days but a week later, I'm still losing hair. Any ideas on how long this will continue?

t go into remission so now they are having me take arimidex which works like tamoxifen. Blood work on wednesday to see if it is working --- I had three tiny cancer nodules left after 6 months of Doxil which is what the arimidex is supposed to keep under control -- my CA125 was 214 after the Doxil and was down to 117 after 6 weeks of arimidex so I have my fingers crossed. Apparently tamoxifen works until it stops working and then you can't use it again.....

Been on Arimidex 26 months. Having numbness in hands and feet. Oncologist doesn't think it's related to Arimidex. Anyone have this problem while on this drug?

I am 4 weeks post radiation and I too feel a bit tired.The headaches I get, are something like you describe..... not a real headache but like if I have a slight head cold or sinus pressure. Now,I don't know if this is solely because of the radiation because I'm also taking Arimidex which also causes a bit of a headache.Do you take any medication,like Arimidex or Tamoxifen?.Please let us know.Thank you.

Armidex may not prolong his growth period much longer with such an advanced bone age, it is a medication used to block estrogen effect, also used in breast cancer, there are concerns with the liver but if monitored carefully most have few side effects. However with a bone age of 17 1/2 growth is near completion. I would work with the peds endocrinologist and talk with them to discuss your concerns, plan of care and monitoring.

Hi Everyone, After 3 months of Femara I suddenly developed carpel tunnel syndrome. My entire right arm became numb in the middle of the night; I thought I was having a stroke or heart attack. I called Novartis & they sent me the requested 9 pages of info about musculoskeletal side effects, the most common being carpel tunnel & trigger finger. I saw a hand specialist who provided hand braces and said I would eventually need the surgery.

I had an ooferectomy almost 2 weeks ago as a precaution, as my mother died of ovarian cancer at the age of 59. I felt great until I started Arimidex on Tuesday, and now I feel horrible. I feel constantly tired and weak and my mind is not alert, I'm having trouble focusing on simple puzzles. I've also been emotionally fragile since Tuesday, crying or on the verge of crying. Will this pass?

I started taking Arimidex about five months ago. 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.

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!

I had a lumpectomy, radiation and now Arimidex. How likely is this tumour with no vessel or nodal invasion present, onco type dx score in low recurrence, to metastasis?

How arimidex works

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