arimidex rib pain

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.

A second one was done on the left breast (which had cancer stage 1) followed by 37 treatments of radiation, 1 week booster. I too have pain in my rib cage on the left side. I spoke with my raodiaoligist/oncologist who said that it does take 12 -18 months for your body to get back to normal. REMEMBER IT HAS BEEN TROUGH ALOT. Give it time. Everyday something even alittle will feel better.

I am on the 5 year plan and prescribed arimidex. The side effects of arimidex are miserable and I stopped taking it for several months until my oncologist chewed me out for not taking it. So, I'm back on it. Every survivor's nightmare is the return of breast cancer, so I am very scared. Any help?

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!

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 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?

My bones have been effected by arthritis and then I found out I had Fibromyalgia ! My pain did increase when I started with the Arimidex and my doc put me on Tramadol, works most of the time for me . Really cold weather and damp do make it worse and I am now into thermal underwear lol ! I too feel like 90 when I wake too ! Not a good start to the day . I also do the shuffle to go to the loo in the mornings as my joints are all stiff .

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.

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..

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 thought I was getting along well with Arimidex but began to have severe knee pain that caused me to limp during the day and woke me at night. I'm just starting Femara.

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 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?

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 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 have taken it for 10 months and it has destroyed my knees, i cannot walk without cruches and am in extreme pain all the time. before starting on this drug I had a bone scan and my bones were fine. jocie 28a xx love and best wishes to all out there. This discussion is related to <a href='/posts/show/557518'>Arimidex has caused my hip to degenerate</a>.

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.

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.

s been 9 months now since I started Arimidex and so far, the side effects are (Thank God) minimal.I too have arthritis and the pain is really not much worse than before.Each person reacts differently to certain medications and if you see that the Arimidex does give you too many problems,your oncologist can prescribe another one that will suit you better.

I am posting again to ask a question my friend that is taking Arimidex for grade 1 breast cancer. She has been taking Arimidex for about 6 months now and has had a hallucination. Has anyone had this happen. I read it may be a rare side effect but it isn't on the package insert.

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. .

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 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?

Arimidex rib pain

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