arimidex dose steroids

Can anyone tell me anything about half dose of arimidex. I recently started with the 1mg dose of arimidex (standard) and feel horrible. Tired, shaky, mental fog, very emotional. I weigh only 124lb and recently had my ovaries removed, so my question is: why do I have to take the full 1mg of Armidex when women who are heavier than me and still have their ovaries take the same dosage. Will a half dose or every other day dose be just as effective for me?

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?

30am, at 12:30p I went to bed for a few hours. Long story, short....I've been feeling horrible since last Tuesday. No energy, very tired and shaky, MENTAL FOG, very emotional, I've cried at least one time everyday since. Even when I was diagnosed with BC i believe I cried only once. I feel I can't do this for 5 years. I tried 1/2 pill yesterday to see if there is any difference, I think there is.

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?

Im taking a 5 day course of high dose steroids for my relapse. I get the dose in the morning and notice my pulse rate slowly rises during the day . At rest it is 95 and I can hear my heart pounding while I am trying to sleep which makes me more anxious. My chest feels sore too. I keep generally very fit and healthy apart from RRMS and my heart rate is only this high normally when I am recovering from exercise. My BP is good thankfully.

I took a one time dose of 40 mg of prednisone along with albuterol this past weekend due to being in an asthma attack, and Iam still experiencing side effects from the prednisone. How long does a one time dose of prednisone stay in your system, and how long can the side effects last?

Hi - after I finished chemo and starting rads in 2003 I was prescribed tamoxifen, took it for 2 months and my Oncologist changed me to Arimidex (one of the aromatose inhibitors) which I think has a 50% better prognosis for non recurrence than the old "gold standard" tamoxifen. I was thrilled, as it had just come on to the market here in England. However, 4 yrs down the line, I stopped it 4 weeks ago, due to severe bone pain (hips, hands and feet) and the pain has gone!

I then had 4 cycles of Adriamycin and Cytoxin. I have now nearly completed 5 years of Arimidex, My Oncologist ir recommending that in October I change to Femara secondary to a clinical trial which has concluded that I am at some risk of the cancer still recurring. I am unsure about this as the side effects of the arimidex hot flashes, weight gain etc causing me to be on a high dose of Effexor are quite debilitating at times.

Over the past 12 months have taken medrol dose packs for fluid in the ear. When do I have to become concerned about side effects. How much is too much. Have recently had a flair up tinnitus and doctor has prescribed dose pack for me if I would like to try it.

So very sorry to hear of your wife's spread but you sound a wonderful caring husband - she is very lucky to have you. Regarding Arimidex, after a WLE,and total axillary removal 5 yrs ago, I had 6 FEC chemo and 25 rads. During rads I was prescribed tamoxifen, took it for 2 months and my then Onc (discharged me after chemo and rads and since retired so I have no one now) switched me to Arimidex.

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?

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.

He advised that the serious and typical side effects of lower dose, long term oral steroids are not seen when these same meds are administered at high doses for such short courses of treatment as that which he has provided me. He also advised that there is emerging evidence in more recent follow up studies to those referenced above, that supports the efficacy of oral steroids for MS relapses.

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.

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?

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.

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?

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.

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.

I have another question. How much is too much of the steroids? I heard that taking it too much can weaken your bones. And I sure don't need that since my mother has osteoporosis and my grandmother had it too. I'm just finishing up the 6 day package they gave me to help with my sinus infection. The thing is, I didn't think about it but I've already had 2 steroid shots in my heel this year and the podiatrist said I can only have 1 more for the year. He won't do more than 3.

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>.

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!

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!

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 Hypogonadism treated wth testosterone and arimidex. I do wonder if arimidex can trigger afib. I have OSA and wear CPAP at night......Also during my sleep study I had a couple central apneas too.....So I wonder if I rally have a mixed Sleep apnea. I am 34 years old.

I had a reaction on two occasions to the Taxotere during infusion. I was given higher doses of steroids to complete the last two infusions. I experienced the bone pain during treatment, but it had all gone away. 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.

Though there is a good theoretical basis for the use of arimidex on endometriosis, I believe that this is still an off-label indication for the drug and the clinical basis for its use is still from phase II clinical trials (studies with still low number of patients). Until such time that the indication of endometriosis can be demonstrated in large phase III clinical trials, the use of arimidex for endometriosis is still controversial.

Arimidex dose steroids

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