Arimidex and femara

Common Questions and Answers about Arimidex and femara

arimidex

Avatar n tn 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
503702 tn?1276176714 Just started arimidex for 9 days and had nasuea switch me to Femara. Anyone having good results? Im in recurrence of OVCA after 15thms. did chemo and avastin trial. Thank you.
Avatar n tn A Web site to visit for information about the side effects of Arimidex and the various chemotherapies is www.chemocare.com Best wishes...
Avatar f tn Estrogen and progesterone positive. If anyone can tell me something about Arimidex and the above side effects and osteopenia and whether or not I need to start a bisphosphonates please let me know.
1030058 tn?1252253572 What are my risks if I choose to just stop the Arimidex and not continue with a change to Femara...My oncologist thinks the risk is there because of the Her2neu but she herself says she is extremely conservative. Also I did not receive any herceptin, I was 18month to 2 years post diagnosis when that was cleared and my previous oncologist (in California) felt the risk outweighed the benefits for me. I would like some advice to help me make an informed choice.
Avatar f tn Thank you for responding; it's so reassuring to know I may not have permanent damage from Femara. Novartis said in the report I obtained on line that most symptoms abate after about 30 days. I have read some things on another site about a young woman about 42 who stuck it out 6 years and never regained her pain free status. I know we are all different & react differently. Did you first try Arimidex or Femara? My Onco.
Avatar f tn 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.
107366 tn?1305680375 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 (I actually have Ovarian cancer, not Breast Cancer.
Avatar n tn 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.
Avatar n tn t want to take fossamax or any more drugs than necessary, but also do not want a recurrence of breast cancer. Is there a clinical study and shows femara vs placebo rather than femara vs tamoifen (novartis trial)? What is the general recommendation? Can you stop femara if side effects become a quality of life issue? Thank you.
Avatar n tn 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.
Avatar f tn 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.
Avatar n tn t used Femara yet. I started on Arimidex and after 6 months had to switch to Aromasin because with Arimidex moving my thumbs became extremely painful and it was moving into my elbow and then my hip. Things improved dramatically, then after a year on Aromasin my hips started aching and I dreaded getting out of bed and standing up. I am convinced it is due to the Aromasin. I'm just 53 so that seemed ridiculous.
Avatar n tn My wife was diagnosed with breast cancer 4 years ago and her 2 positive, estrogen positive and progestion. She"s been on arimedex for 3 years after radiation,chemo and hercepton treatments. Is there ANYTHING she can do to ease hot flashes? They bother her so bad she wants to quit taking the arimidex.
Avatar n tn Another hormonal treatment is Femara, but it has the same mechanism of action as arimidex and is most likely not to work. Your best option is to change chemotherapy regimen and Gemzar is a good option.
Avatar n tn 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!
Avatar f tn 5 months later counts rising again and tumors on CT scan -- Started Doxil Feb 3 of 2008 and just finished 6 cycles -- tumors have shrunk significantly by CA125 up to 256 which is where I started in Feb (had gone down to 161 and then started climbing again) -- docs say I need a break and have started me on Arimidex two days ago to control the CA125 -- should i be continuing the Doxil to make the tumors continue to shrink, or stay on Arimidex until the tumors are growing again?
107366 tn?1305680375 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.
Avatar n tn After my lumpectomy and radiation sessions,I first started taking Arimidex for 3 years.This drug caused a lot of pain and aches in my bones and muscles.My Surgeon told me to try Femara to see if I could better tolerate it.So I took Femara for one more year.The side effects were much less aggravating,but it still caused fatigue, arthritis,indigestion,muscle pain and weight gain. Finally my Surgeon told me to stop the drug and I did. In total I was taking these drugs for 4 years.
Avatar f tn 2nd I am trying to be on an estrogen blocker as it was estrogen positive, currently trying Arimidex as fumara gave me too much pain have you tried these drugs right after chemo and with any luck. We are also looking at it as preventive for breast cancer. I am 54 years old and doing well.
Avatar f tn I hope your Holidays are filled with lots of family, love and laughter.....and that your New Year is finally filled with lots of good health and good times. Peace to you both.
Avatar n tn Then I tried Femara and on that one I lasted for a few weeks before I quit, and then Aromasin and that was about one day. (All of the above except for the Tamoxifen are Aromatase Inhibitors) But of all the things you have said, the oxicontin addition is the worse, I think, and really irrisposible to hand out at this time and for this reaon.
534810 tn?1213327718 I, too, have joint pain and swelling in hands (and sometimes feet) w/femara. I have developed a trigger finger and dequervains tendonitis in bilateral wrist w/thumb pain. Had to go off med for a month and also have sites injected w/cortisone. Never had any of this before. Oncologist said she had seen trigger finger before no dequervains tendonitis? Wondering if anyone out there has had any of these side effects? And what do you think of this? I am miserable w/all this discomfort.