Evista and osteoporosis
Common Questions and Answers about Evista and osteoporosis
evista
t know that you should be taking evista and tamoxifen together , but the evista is definitely not a estrogen receptor. And who knows, maybe with them both it will help ward off further cancer problems. Just be careful because both can cause blood clots -- ask about taking lose dose (81 mg) aspirin or 1 mg warfarin to prevent the risk of clots.
P.S. I am in the middle of treatment for another recurrence -- the evista didn't prevent an ovarian recurrence....
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.
He said that I am at high risk for bc (despite breastfeeding and full-term pregnancies before age 30 and onset of menstruation at age 13 and menopause at 52 and healthy weight, etc.) and that going forward I should be tested every six months with MRI and mammogram, alternately. He also said an oncologist would later discuss prophylactic treatment with tamoxifen or evista (I have osteopenia, and he said evista can be beneficial for that). I am very frightened and anxious.
Doctor gave me an antibiotic but again next week it recurs. Body aches mostly knees and ankles [ i suffer through osteoporosis and joint pains too but the pains were not troublesome earlier] Can anyone tell is it viral or anything else.
I am no longer taking Evista, but while doing some research to see if I wanted to go back on it for my osteopenia, I found some references to a correlation between Evista and ovarian cancer and wondered if that could have had a bearing on my case.
This discussion is related to <a href='/posts/show/395649'>Evista and Ovarian Cancer</a>.
I researched Evista online and found that it is linked to increased risk of ovarian cancer and stroke, in addition to other nasty symptoms I have never experienced (including hot flashes, night sweats, insomnia). I am afraid to take this drug, too, and don't know what to do. Has anyone else been in this situation?
Hi,
Hair loss in a known but not highly common side effect of Evista. If you do a search: "Evista and hair loss" you will find numerous references to this side effect.
This link:
http://www.ehealthme.com/ds/evista/hair+loss
indicates that as of Sep. 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.
I am currently on Copaxone, Depakote, Neurontin, for the MS; Evista for osteoporosis, Tenormin, (as a beta blocker),for Migrane headache, Cinestin - an estrogen replacement (I had a complete Hysterectomy in 1991), Vesicare and Oxytrol for my neurogenic bladder and Tylenol with codine for acute pain. I recently had blood work and my WBC was slightly elevated at 11, RBC, Hemoglobin, and Hematocrit were slightly low and my lymphocytes were above 5000, (high normal is 3900).
I am currently on 2 osteoporosis medicines (Evista and Fosomax) in attempts to stop the microfractures from occuring. After a few months of taking these, I did improve. However, my hips and back recently started bothering me again, in the form of spasms. I cannot get another MRI for a few more weeks. I take Naproxin 2x's/day and muscle relaxers 1-2 times/day. Acupuncture gives me great short term relief, but the spasms are back the next day.
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.
Tamoxifin can cause blood clots and uterine cancer. Evista is a little better in the side effects I believe, however everyone is different. I also have ADH(atypical ductal hyperplasia) and it increased my risk from 1.6 to 3.2 which is doubled, so I am considering the same thing. I am also having pathology reviewed by yet another lab to be sure it is not DCIS, which I am sure the other pathology report is no doubt correct. The best thing for you to do is to research. Then make your decision.
I am currently on Copaxone, Depakote, Neurontin, for the MS; Evista for osteoporosis, Tenormin, (as a beta blocker),for Migrane headache, Cinestin - an estrogen replacement (I had a complete Hysterectomy in 1991), Vesicare and Oxytrol for my neurogenic bladder and Tylenol with codine for acute pain. I recently had blood work and my WBC was slightly elevated at 11, RBC, Hemoglobin, and Hematocrit were slightly low and my lymphocytes were above 5000, (high normal is 3900).
Either estrogen replacement or Evista are good choices in prevention and progression of osteoporosis in postmenopausal women. Evista may also protect against uterine and breast cancer. If you don't have true osteoporosis, and you are headed in that direction (osteopenia), then estrogen (or Evista) therapy is more appropriate for prevention, than the addition of Fosamax. At the point of osteopenia, Fosamax may be used at reduced doses for prevention of the progression to osteoporosis.
Mum was diagnosed March 2005 OVCA stage 3, reoccurance 2007 and 2008, each time treated with carbo and taxol. Currently in remission. Dr put her on femera and tamoxifen but since being on tamoxifen she has had 2 DVTs in her right leg. Dr today stopped them and put her on warfrine (sorry about the spelling). Dr thinks she might have to be on this for the rest of her life. Dr also said she expects mums cancer to come back at some point but her cancer is very slow growing.
My blood pressure at the bloodmobile yesterday was 102/70. The only meds I take are Evista to prevent osteoporosis and Topamax for neuropathy from the chemo (it's helped greatly, I can walk barefoot again). Because I work nights I occasionally take a quarter of an Ambien to get to sleep to put myself back on a "normal" sleep pattern. Don't drink coffee or tea. Since it started,I always feel this when laying down, sitting up only when I am very tired.
to be tollerable. Now I start Evista for lcis and osteoporosis. That is supposed to cause flashes. My doc says Effexor and Clonidine will help flashes. I do not want to take Effexor, and Clonidine may lower my blood pressure too much since I am already on two blood pressure meds. I will try the Evista and if get flashes again, I may just stop. I read magnesium helps, so I tried. It did help quite a bit, but unfortunately, if you take enough, you get diarrhea. Some choice.
Osteoporosis is a common condition where the bone becomes thin and fragile, creating an increased risk of fracture. Osteoporosis is usually painless until a fraction takes place, and osteoporosis is a major contributing factor to bone fracture, including hip fractures, which are more common as people age. There are almost 2 million hip fractures annually around the world. While in the U.S.
I had estrogen positive stage 2 breast cancer eight years ago. I had my overies and breasts removed because I have a family history of breast cancer. I' m currently taking Evista and my estrogen level is the same as a mans. Am I out of the woods yet?
I take Synthroid for hypothyroidism, and I was diagnosed with osteoporosis, I have tried several times to take calcium supplements within the guidelines when taking Synthroid, (more than 4 hours before or after taking med), and I become almost immediately exhausted, and sleep for 8-12 hours. I take only about 250 mgs of calcium, and vitamin D as well.
My doctor told me that I have Osteoporosis and wants me to try Forteo an injection for two years. Has anyone tried this drug and what were your side effects, if any. I don't want to make my stomach problems worse than there already are.
I have started mega doses of supplements and calcium and D and excercise and I want someone to tell me that that has worked for them. Most comments I get is to take the drug because it's more effective. I can't believe everyone is taking bisphosphonates or other drugs like that.
Please let me hear from you if you see this!,,, Thanks, and hope you are doing well!
I just had my frist Bone scan and the office called me and said I had osteoporosis and that they called in RX for Atelvia..
I picked up the RX and was reading the information and I am concerned about the side effect of this medication.
Is this the only way to help with osteoporosis? Is there anything elso another way?
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