Evista side effects
Common Questions and Answers about Evista side effects
evista
15, 2013, 17,635 people were reported to the FDA to have side effects when taking Evista. Among them, 259 people (1.47%) have Hair Loss.
Time on Evista when these people had hair loss:
< 1 month 4.35%
1 - 6 months 4.35%
6- 12 months 8.70%
1 - 2 years 26.09%
2 - 5 years 39.13%
5 - 10 years 17.39%
10+ years 0.00%
As japdip counseled, all concerns about your treatment should be discussed with your oncology team.
I finally seen an oncologist today because of the pathology report showing I had atyhpical hyperplaisa/carcinoma in situ.he said I am cancer free right now, but a high risk of getting breast cancer so he is recommending this medication Evista. Of course there are side effects now what medication doesn't have any side effects right.Has anyone taken this medication of Evista an had bad side effects or has seen great results in preventing getting breast cancer?
No, I haven't, sorry. But this was my experience. The first week, or so, I felt like a complete 'zombie', and I think my bones also hurt. Then, it got better.
I have all the menopausal symptoms; I cannot sleep, the hot flashes, moodiness, etc. The hot flashes got worse after a few month. I have been taking clonidine, a high blood pressure medication, for it which really helps. It aslo helps you sleep and is very sedating at first, but very short term.
Is there any drug interaction between these two drugs ? I am taking Evista for Osteoporosis.
Could my recurrence of Ovarian cancer be attributed to my taking Evista for a year? I had ovarian cancer 15 years ago and after surgery and chemo, and a "second look" surgery with multiple biopsies was considered cured.I had a complete hysterectomy and the cancer seemed to be contained in my left ovary. Last winter I found a lump in my left groin which was biopsied and diagnosed as ovarian malignancy.
Since radiation is a local treatment, side effects are usually confined to the area being treated. Radiation treatment to the chest may cause problems when swallowing, cough, or shortness of breath and breast soreness and/or swelling. I am not sure which medication your mother is taking, but Evista (raloxifene) can cause muscle cramps of the legs. Please have your mother make an appointment with her physician.
I had not personally heard of the the fractures (femur) from the Fosamax, but I did hear of the other risk factors for some of the older drugs. I had heard also of the side effects like hot flashes and sweats which are none too pleasant. My doctor usually advises me that the benefits often outweigh the risks. After hearing about the cancer risks and stroke incidents, I was not too sure. I became pregnant when I was 35 and therefore could not take any drugs.
Has anyone heard of taking Tamoxifen or Evista as a possible step in breast cancer prevention? My doctor has suggested it because I'm in a high risk category. I'm not sure what to do.
Based on your personal medical history (keep in mind that you well might not have the same risk for the side effects your mother experienced, take into account your healthly lifestyle and different body type), your PCP and oncologist can collaborate in weighing the benefits and risks of using one of these drugs to lower your risk for breast cancer. Women with present or past blood clots in the eyes, lungs, or legs are cautioned about taking these drugs.
Because of my GERD, my doctor prescribed an IV infusion of Reclast. Unfortunately, I suffered some of the side effects, fever, and severe bone pain to the point of not being able to take in a full breath. My doctor was so concerned he put me on a steroid dose pack to reduce the reaction. My body doesn't seem very tolerant of any drugs, couldn't take anything other than extra strength Tylenol for a foot surgery. I will have to figure out something else with an endocronologist?
Hi, I'm ok, but I think about this every day since I found out. It bothers me more than I thought it would. I have no known family history, but my mother died at 60 from complications from uterine cancer. I am post menopausal. When I was 49 my husband died and my periods just stopped suddenly and I had only hot flashes. But they were often and I would get drenched at work. So I took Prempro. I never stopped taking it because every time I tried the flashes came back.
Some of these drugs are quite potent and may have unwanted side effects. Be sure to discuss all of that with your doctor prior to taking them.
The other option is the surgery. You should go to your doctor and get checked. Sometimes, gynecomastia by fat deposits, but won't necessarily go away with diet and exercise. Mastectomy can be done endoscopically, which is much less invasive than a normal surgery.
You are 74 and done with menopause, now it is up to you to decide what you wish to do, if you can get a second opinion from another Oncologist. I am the kind of person who believes that life quality is far more precious than life quantity. I am 69 and I have decided that no more treatments for me, I am done. Ask yourself and your trusted oncologist the following: 1] How much longer will I lead a quality life if I don't use any Aromatose Inhibitors?
Hi and thanks again. It sounds like you've been thru a lot with the chemo and then side effects. Yes, impossible to sleep and does interfere with daily things. I drink coffee to stay awake during day which probably doesn't help my insomnia. Have a good day.
Hi,
Even with a total hysterectomy,the body will still produce some estrogen which is effectively blocked with an aromatase inhibitor (such as arimidex,Femara etc). In one study, aromatase inhibitors were found to offer greater benefit than tamoxifen in Post- menopausal women.Tamoxifen blocks the estrogen especially to the breast tissue. This is an important distinction because aromatase inhibitors cannot be used in Pre- menopausal women.
I will do that it seems the higher dose has created this and I'm not on anything else.
Many AD's have side effects that affect the libido, guess it applies to both sex es. As far as I know all AD's have this drastic effect . Hopefully you'll find one that's OK for you . Good luck.
Yes, I've only been on it a week and I experience the muscle aches and bilateral flank pain as well. In addition, insomnia!
THOUGHT I WAS GOING CRAZY BEFORE I FOUND YOU GUY. SIDE EFFECTS MUCH MORE THAN WE HAD BEEN LED TO BELIEVE.PERSONALLY HAVE THE BLURRY VISION, ENHANCED JOINT PAIN, SWEATS, AND SLEEP NOT GOOD. FINALLY SAW FEED BACK FROM THE COMMUNITY THAT VERIFIED OTHERS FEELING SAME. ANYONE FEELING ANYTHING ELSE ODD? PLEASE POST. ALSO HAVE BLOATING, IRRITABILITY. AND CONTRARY TO WHAT DOCTORS SAY, I'M ALWAYS CONSTIPATED.
Hi. I am on week 60/72, second round of treatment. I was really really sick after shot for first few months and then this resolved and became tolerable at least. I now find that I am having these same significant side effects later in tx. This didn't happen last round, but I went 48 then. Anyone else have this happen?
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