Fosamax side effects mayo clinic
Common Questions and Answers about Fosamax side effects mayo clinic
fosamax
Good morning,
I saw my Dr. this morning and he would like to start taking fosamax,after reading all the side effects i'm not sure i should.
After recovering from Stage 4 Kidney Failure, after 4 years off Simvastatin, which caused it, my doctor recommended an MRI with and without contrast. I objected to the contrast dye because I knew about the risk of NSF (Nephrogenic Systemic Fibrosis). He assured me that my kidneys would flush it out of my system in 24 - 36 hours. 4 days later I awoke with both hands clenched tight and opening them was painful.
My wife is a 65 year old in good health who has taken FOSAMAX for 5 1/2 years. She wants to get her teeth straightened. The periodontist has recommended a procedure to reinforce the gums prior to the braces. This has added an additional 6K to the price and about 3 months to the total time to straighten the teeth.
and this is to help keep nasal membranes moist as well. An ENT doctor at Mayo Clinic told me to use this as well, even though I have Vasomotor rhinitis. Hope this is of some help to you I would go and see an ENT doctor though. and be honest with him about your past use of cocaine., as this could help with your treatment of your nasal problems.
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.
I saw a Professor of Endocrinology in Feb 2008, referred by my bc surgeon, as this guy has an academic interest in side effects of Arimidex. He suggested I continue with Arimidex and Fosamax to prevent further bone loss, but I cannot stand the pain and disturbance to my sleep.
Does anyone have any experience of stopping Arimidex and getting a different med that does not have the side effect of bone pain?
Thank you so much for taking the time to respond, it is greatly appreciated. My last vaccine was over a week ago, and I have seen some fluctuation of the side effects since this post as well. They are fairly steady and constant, but I have noticed a decrease on occasion so am hopeful they may all pass soon. I’ve also began utilizing OTC pain meds daily which do help tremendously the constant headache.
I have been at the Mayo Clinic for the last week. It has been a very pleasant experience, given my circumstances. They have been very efficient and very informative. They have treated me like a person and not just a number. I am very impressed.
I am looking for some personal advice on medications. I was dx with CIS due to the fact that I am not really experiencing any symptoms other than the optic neuritis, which has resolved for the most part.
Has anyone responded to your question? I was recently diagnosed and heard that Dr. Gray at the Mayo Clinic does have some expertise in treating this disease. Of course, my insurance does not cover the doctors at the Mayo Clinic. I have been seen at the UCLA Revlon Center, but they really have no expertise in this area, so I feel like my treatment has come to a standstill.
To Nee08 Thank you for the reply, is nice to know that someone else out there was having the same problem as me. I also stopped taking the medication for bone health too. You may be interested in reading an article about it written by an ob-gyn on this website, I forgot her name, but you can get it here. Very very interesting, and I'm sorry that I started taking it in the first place without questioning its side effects.
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.
Truthfully, I've heard one of the best MS Clinics in the US is the Mellen Center at Cleveland Clinic. You might try checking out http://www.mscare.org
They list all the clinics available, etc. My neuro said the clinic at Cincinatti isn't that great but thinks Cleveland Clinic is really good. I've never heard of the Mayo Clinic being highly rated for MS, but more for heart desease.
I'm new to this site. I was diagnosed hypothyroid eight months ago. At the time I didn't really have a lot of symptoms - before that, my doctor was investigating why my cholesterol level was so high, as my diet/weight etc are all pretty good. I spent six months trying to bring the cholesterol into the normal range - and succeeded (although it's still on the high side - the doc was happy) just by cutting down on dairy foods.
When my TSH level was discovered to be 5.
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