Food and Drug Administration raised concerns about the potential for some serious side effects in women taking bone-building drugs called bisphosphonates, specifically Fosamax, Actonel and Reclast. The published findings are not new.
I know that the early hysterectomy has caused my bone issues(been on Fosamax and actually just started Reclast this week -2.7) but I wonder if it is effecting the breast? I went in for my annual mamo last week and have been called back yet again. New spot directly under the nipple, same breast. Sheduled US for next week. So two mamos and 2 call backs...I am nervous..is this common, should I be worried, is this what I have to look forward to every year...
MY FRIEND HAD TO HAVE INVASION DENTAL WORK, BUT WHEN THE DENTIST DISCOVERED THAT SHE WAS ON FOSAMAX AND HAD BEEN FOR AN EXTENDED PERIOD OF TIME, HE INSISTED THAT SHE TAKE A HIGHLY SOPHISTICATED BLOOD TEST. SHE HAD DIFFICULTY FINDING A LAB THAT WAS FAMILIAR WITH THE TEST AND ONE THAT PERFORMED THE TEST. THE RESULTS OF THE TEST INDICATED THAT HER JAW BONE WAS NOT SUFFICIENTLY STRONG[?
http://www.medhelp.org/posts/Breast-Cancer/can-bone-spur-be-caused-by-Arimidex-or-fosamax/show/1441530?personal_page_id=1709244#post_6565716
Best wishes...
Fosamax has been linked in long-term users to the development of low-impact femoral fractures. In the event of a fracture fosamax may interfere with remodeling and healing. However, the decision to continue or quit would need to be taken by his treating doctor; keeping in view the initial condition for which it was advised and the risks Vs benefits. You may like to discus in detail with his treating doctor.
Hope this is helpful.
Take care!
My mom is taking Fosamax [Alendronic Acid], she is taking it exactly as directed and is still getting terriible burning in her esophagus. She is really suffering. She says there are no alternative medications she can switch to.
Are there any remedys she can take to help ease the burning in her esophagus? Supplements, Vitamins, anything like that?
Any help anyone can give me would be greatle appreciated, as i Said, she is really suffering
Thanks in Advance!
Do you mean Fosamax (alendronate)? If you do, its for treating bone problems like Osteoperosis by adding bone mass and slows bone loss. I use it for Osteopenia.
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?
35 years of empty sella, hi prolactin, testosterone injections, osteopenia, broken ribs and recently hip - and now at age 67 two of my children ages 33 and 36 flunk Dexa scans and are prescribed fosamax, which they refuse to take until hyperparathyroid is ruled out. I get labs showing PTHs of 63/(15-65), 51 and 45, with ionized calciums of 5.2, 5.3 and 5.4 on scale 4.5 - 5.6. Three endos and 2 GPs say it's all coincidental. Should we get treatment in Europe?
I am a "heart patient" and have been taking Fosamax to improve bone density. Lately I have seen several things that implied I might not should be taking Fosamax. I would enjoy hearing some opinions on this matter.
Thanks.
I have been on Fosamax for almost a year . In the last few months I have developed really bad heartburn. Zantac helps for a few hours but then it starts again.
So I told my doctor that I wanted to increase my intake of calcium and do a wait and see on the Fosamax. She told me that she's not worried about me for now but for what may happen to me in 20 years. The scenario sounded horrible--breaking a hip and dying--if I didn't start treatment now. But she conceded and we agreed that I would be screened again in a couple of years.
I am amazed at how the pharmaceutical companies drive diagnosis.
DEXA scan showed increased bone density loss to that of a DEXA scan done before bc (ordered by gastro due to 30+ yrs of steroids). BC surgeon prescribed Fosamax and Calcichew/Vit.D3. A bone scan showed osteo arthritis in both hips, hands and feet. No meds prescribed. I am on weekly injections of 12.5 mg methotrexate for Crohn's.
My GP suggested I stop the Arimidex for 3-4 weeks to see if the pain diminished, which miraculously it has.
He looked at me as if I was nuts when I told him I was even on the fosamax, and recommended I stop it altogether. Having said all that, I realize many many need the med, but I guess my suggestion would be to see an Ear/Nose/Throat doctor - he may have some suggestions for you, and would be able to see if any damage is done. Best of luck to you!
What did your prescribing doctor say about the side effects caused by the Fosamax and how to deal with it?
I understand your feelings about how the facial pain affects your quality of life. Because it's something people can't see -- it's sometimes hard for our families/friends to understand. It took me a long while to get my husband to understand what I was dealing with, with symptomatic TN.
That's terrible! I would search for any lawsuits against the manufacturer of Fosamax for injury like this resulting on facial bone loss and tooth loss. Seems to be me they should pay for any corrective dental or medical treatment and pay compensation for pain and suffering. I've read negative things about this drug and it's ironic that it is advertised as preventing bone loss, and yet it accelerates it.
Recommended
