Arimidex back pain
Common Questions and Answers about Arimidex back pain
arimidex
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!
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.
t any osteoporous Femara causes swelling and bone pain I switch to Arimidex after being off Femara for 2 weeks and am not having the pain. Please look in to Femara side effects and possible changeing to another drug. I even was in physical therapy for two months because I thought it was me but no it was the drug..
1. Go back onto Arimidex for one week and see if hip pain returns. Absolutely unacceptable.
2. Take tamoxifen - again unacceptable, as prognosis for non-recurrence is better with an IA.
3. Switch to Femara or Aromasin
4. Referral to a bc Oncologist at my hospital - he finally hit my button!
He is referring me to a female Onc with a special interest in not only bc, but lymphoedema, which I unusually have in the affected breast, but not arm - I never "present" normally.
About 1 yr after finishing rads I started having horrible chest,rib and back pain, Dr put me on gabapintin 800mg 3x day +20mg 3x day oxycotin and 5mg fr oxycodone for breakthru, Ive had 2 bone scans mri ct in the past 2 yrs, my pain still haunts me, I also have a lump on my left side just below ribcage and it goes around to my back near my kidney and about 2 -3 months ago my hands legs feet started getiing tingley and when I wake in the am, my arms are numb, I also have lower back pain.
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. Aromasin permanently binds to the Aromatase and Arimidex is temporary. I'll have to do more research about what that means chemically.
I have endometriosis stage 4, I had 2 surgeries in 2006, and my surgeon is putting me on Armidex to try to control the pain. Is this a common use for this medicine?
The headache feels like a constant squeeze around my head.No pounding or sharp pain exists however they persist.My doctor says this is not associated with radiation??? I am otherwise a healthy strong and active professional. I would appreciate feedback ...am I alone with these symptoms?
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.
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.
The next year the cancer was back and she had a mastectomy. My question is since my tumors were small even if they were estrogen fed shouldn't the mastectomy have been enough. I really don't want to take this medication as I already suffer with fibromyalgia and many of the other "side effects" of this drug. I'm very confused and would appreciate anybody else giving my their opinion on this.
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.
This time it mastisized to my right femur which was treated with 10 treatments of radiation. The breast was removed. I have been on Arimidex 6 years now. 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 am 42 and have been on Arimidex since Feb. 20, 2009. I have had a hysterectomy in May to remove my ovaries.
I have gained 15 pounds. I am on a 1600 calorie/day diet and walk six miles a day, four days a week. I would like to know if there is any thing else I can do to battle this weight gain. I will be on Arimidex for another four years.
I have been on arimidex for about 2 months (since Feb. 2009), switched from tamoxifen after 1 year on tamoxifen. My white blood cell count the month before I started arimidex (Jan.) was 4.2. When I had a blood test more than 2 weeks ago (April 8), my WBC count was 3.3. Could this be a side effect of arimidex?
FYI -- I was diagnosed in May 2007: IDC, stage 1, 1cm., e.r. +, grade 3, negative lymph nodes. I had chemo (1 infusion TC, 6 infusions CMF) Aug. 2007 to Jan.
The cancer has not returned (I take Arimidex). However, I my ribs underneath my breast are very painful - they can hardly tolerate any touch or pressure. My Oncologist has told me that every women she has treated for the same also complain about bone pain on the site where the radiation took place. What is the reason for this? Could it be a weakening of the bone structure due to the medicine, or did the radioation cause it?
Thanks,
R.K.
After seeing an endocrinologist who ran all types of blood work which came back normal with the exception of his estrogen level a bit higher then normal and had an X-ray of his hand which showed bones of a 13 half to 14 half yr old (I was told was good ) want to give my son arimidex. My question is......is this safe for teen boys. I read its not FDA approved for children.
After some 4 yrs on the AI the pain in my left hip, both feet and hands has become unbearable and my GP advised me to stop Arimidex for 3-4 weeks to see if the pain diminished. It has thankfully, so I believe Arimidex was the culprit. I see him next week and hope he will refer me to a new female Oncologist at my hospital, who has an interest in both bc and gastro, as I have weekly injections of methotrexate for Crohn's.
My oncologist is in the process of deciding whether to prescribe Letrozole/Femara or Anastrozole/Arimidex. What considerations factor into which of these two drugs to use? Has anyone had experience with either of them? How serious are the side effects?
I couldn't take tamoxifen am know now am on arimidex. although at times i feel stiff it is better than tamoxifne and for get about femarar i felt 200 years old. i am estrogen positive which is why I am on arimidex It sometimes makes me achey and sometimes my stomach bothers me but i go off for a couble of days and then back on it.
Hello. I am taking Arimidex (dx May 2007, IDC, 1 cm., grade 3, negative lymph nodes; had lumpectomy, sentinel node biopsy, chemo, radiation; I was 54 and perimenopausal at time of dx and chemo put me in menopause.) I also now occasionally consult a holistic MD (referred by my oncologist) for nutritional advice.
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