Many women with RA, especially those who have taken prednisone, could be prone to osteopenia or osteoporosis. Also, our inability to do lots of weight-bearing exercise can contribute. I was lucky that I had a female rheumie many years ago who thought to order a bone density test that caught it early. Fosamax has brought my bone density back within normal limits, and I continue to take it to maintain.
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.
Other hip and spine are in the yellow zone for osteopenia. I am allergic to Bonita and Fosamax so for now trying exercise, calcium, vitamin D to combat it. My mom has it and I've been menopausal for 10 years now at the age of 43.
I don't take magnesium. Should I be and what would be a good starting dose?
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!
It looks like your FT4 was dropping, as your TSH was rising, which would be typical in someone who is headed for hypothyroidism. Could you please post the reference range for the FT4? While yours look low, according to what my lab's ranges are, these vary from lab to lab, so must come from your own report.
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 have been on Calcium and VitD for 3 yrs! I see you have MD in your tagline, are you a physician? I understand that calcium is leaching from my bones, and I have been on replacement therapy for that. In fact, I just completed the IV Reclast last month. I need to know what else can be done, or do I just have to live with this. By the way, in researching PTH, arrythmia's were a symptom of hyperPTHism.
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...
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.
Hello Emanuelle,
I definitely feel for your concern. Although I am 36 I have pretty severe osteoporosis and at one time was recommended to take medication for it. I have several spinal injuries which have resulted in Degenerative Disk Disease, other joint syndromes and overall bone density loss.
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.
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[?
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.
I am 22 and have just found out I have kidney disease. I do not want to tell my family, because I know they wouldn't deal with it very well. Is it likely to be easy keeping this from them (I live with them)? I am considering not receiving any treament for now to make extra certain family don't find out.
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.
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