evista research

I have had a surgery to remove the tumor and surrounding lymph nodes in my left groin as well as exploratory abdomina l surger and multiple biopsies and 6 chemo treatments with taxol and carboplatin during 2008. 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.

he said I am cancer free right now, but a high risk of getting breast cancer so he is recommending this medication Evista. He said Evista was better then the tomoxafin because it causes less blood clots. Is this true? I haven't started any meds yet, since IM going to get a second opinon first to see what is the best course of medication for me to take.Of course there are side effects now what medication doesn't have any side effects right.

Is there any drug interaction between these two drugs ? I am taking Evista for Osteoporosis.

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.

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.

There are also stage III clinical trials for Ovature out there to make you sensitive to platin again -- my doctor also keeps talking about Navelbine as a possible alternative treatment, although my research showed it mainly is used for small cell lung cancer. The Femara, Evista, and Arimidex and Tomoxifen are all used to try to stall the need for chemo again, but don't make anything go away, they just slow it down if the do anything at all,.

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.

I am 68 and all tests indicate that I am in very good health. For the moment, my only perscription drug is Evista. Where can I go with this question? Thanks.

How long should a woman stay on Evista if no negative side affects?

When a doctor on ABC national news suggested that women stop taking it after 5 years, I made an appointment with my doctor to discuss stopping this med. My doctor agreed, but now suggests that I take Evista. 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.

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. Seventeen years ago I had a benign lump removed in the other breast. Two years ago I had emergency surgery for a retinal detachment and have only just now come to terms with my altered vision the various complications from the detachment.

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).

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.

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.

Two lymph nodes were involved, I had a lumpectomy, lymph node dissection (l5), chemo, radiation, and tamoxifen followed by evista, which I currently take. My mother and her sister both had breast cancer (neither died from cancer). No one ever suggested I have anything but a yearly mammogram, always negative. I am most concerned about my daughter, who is scheduled for the MRI guided biopsy Feb. 20. I also wonder if I should be getting any tests other than the yearly mammogram.

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?

Evista can cause biliary calculus which could 'feed into' conditions that might result in pancreatitis.

Why is it that science and medicine research so much on synthetic chemicals and such yet all these natural items: primerose,cinnamon,aloe era,cumin,etc.... That many of us read on pregnancy website for induction for example haven't been researched the heck out of them? There's so many natural item that by now and how technology is and our advanced medicine that we don't know all about them.

Greetings doctor I am actually doing a research paper on HIV for school and with so much info online from one end of the spectrum to the other I figure I would ask a specialist directly a few questions so here it goes... 1-with testing now a days would you consider 6-8 weeks conclusive? 2-do you believe rapid tests are just as reliable as lab based? 3-do you feel oral rapid tests are just as good as blood? 4-what are the most common symptoms you see with onset of HIV?

I know somebody posted where to go to find out about the research that is going on, and what clinical trials we may be able to get into... but my brain isn't working today and I can't find the post. Somebody please give me that web site. I'd really appreciate it.

Gene therapy has potential, not to recreate lung tissue but to reduce the airway inflammation that results in emphysema, be it smoking-induced or other. Research is underway on gene therapy but the results thus far have been very disappointing. The adaptation to chronic residence at high altitude has been studied extensively. You are correct in stating that bigger lungs have nothing to do with it and that has been well known for nearly 100 years.

Evista research

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