Anyone on Alendronate?
I have been on Alendronate since May 2017. If I don't have osteoporosis, but some osteopenia, how long is it safe to take a 'vacation' from the drug? Does it do any good to take it every other week? My internist wants me to switch to Prolia, which I will not do. I don't know if I would have any side effects from it and it is not a drug that can be stopped w/o possible problems. I am 78 years old and my only health condition is RA, which is under control and has not affected my day-to-day life. I have read that alendronate can affect your esophagus and occasionally, over the years, I have had times where I feel like food gets stuck and it takes anywhere from 3 - 30 minutes for this uncomfortable feeling to go away. I have had my esophagus stretched via an endoscopy several times.
Re Prolia, I have read : People with weakened immune systems are advised not to use to denosumab because it can lead to serious infections that require hospitalization (such as heart infections). It can also cause disintegration of the jaw, called osteonecrosis, and atypical femur fractures. Recent studies have shown that people who stop taking denosumab experience bone loss within the first year if they do not start taking a new osteoporosis treatment. In clinical trials, results also suggest that people who stop taking denosumab and did not start another treatment experienced more vertebral fractures (fractures in your spine) in the 10 months after treatment than people who had been taking a placebo.
I am interested in hearing thoughts about 'vacationing' from alendronate.
Interested in more discussions like this? Go to the Osteoporosis & Bone Health Support Group.
I'm not the one who posted the information but I did find the following post from the same person about drug holidays:
https://connect.mayoclinic.org/discussion/need-an-osteoporosis-drug-vacation/
The recommendation in the post above is for a drug holiday after 5 or 10 years.
Personally, I will never stay on alendronate that long. I was on it for 5+ years and had a vertebral compression fracture while taking it. I feel like I should have come off it after 3 years max.
You didn’t say how often you take the medication? There are a number of formulations available and I wonder if a change in how often you take it might be helpful.
Hi. I am on Alendronate now for 5 weeks. (1x weekly) My symptoms are similar, dry throat, coughing , clearin of the throat contiunosly, a swollen gland that acts up when I eat something spicy, crummy feeling, I was switched to this med after i experieced a bad rash from Prolia (only had 2 injections). I feel ready to give up, but Im trying to hold on.
Hi hmbrglr!
Sometimes it gets a little depressing with the side effects, but I've decided it could be worse and I'm not ready to give up on the Alendronate. I didn't take it on my regular morning, felt guilty that I didn't, and took it the next morning.
Some days the side effects aren't as noticeable as other days. I'm hoping the more recent ones will wane over time. I'm going to talk with my doctor about them next week and I know she'll give me a pep talk.
Be strong and hang in there!
I get it. That’s where I’m at too. I hope we both hang in and will be glad we did.
Newly diagnosed with osteoporosis and will not take Fosamax after reading about its side effects. What is anyone’s thought on peptide collagen and hyalauronic acid to help regenerate bone growth?
Esther