What is minimum period of Alendronate to minimise Prolia rebound?
I started on Prolia in July 2022 on advice from my doctor that the treatment would be for only 4-5 years and thereafter I could stop. I have taken 3 Prolia injections, the last one in July 2023.
Before my 4th injection in Jan 2024, I started doing a lot of reading and decided that I do not want to be on any osteoporosis drug at all. So, instead of taking my 4th Prolia injection and to minimise the rebound effect from stopping Prolia, I started on a weekly dose of Alendronate.
However, I am really not comfortable taking Alendronate as well and would like to seek any advice/opinion on whether I am stuck with taking Alendronate for the next 6, 12 or even 24 months.
What is the shortest period I can be on Alendronate? Or should I just risk the rebound effect and stop my Alendronate now (I have taken 3 weekly doses so far)?
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I did not pay that but that is the charge if you go online for the price of Prolia. I have medicare and supplement so that was covered. I am so glad I got off of it after one shot. But now I am dealing with actonel gagging on food and swallowing issues. Just had bone density. And the average reading is about -2.0
Check out the thread about Quitting Prolia. Once you stop Prolia you need to be checking your CTX. It is important to check it before you start any treatment really. I quit taking Prolia after my 5th injection. I wanted to do it sooner , but was unable to find someone qualified to assist me. I started Alendronate under the direction of my physician 15 days after my scheduled Prolia shot. I did a CTX test. The next day I started the Alendronate. I will be monitoring my CTX every 3 months to monitor where that marker is. I am hoping it will stay under 212.Iif it does not I will need to have a Reclast infusion and continue to watch. The research is not clear about how long the rebound can continue. Monitoring needs to continue for a minimum of a year. Hopefully, this is helpful.
Do you have any side effects
What were your side effects from Alendronate?
I am about to start it.
Fortunately, after 2 months I haven't experienced any that I am aware. I am hoping it is keeping my CTX in check.
Please do not take advice in this subject matter. If you need a second opinion do so! This is very serious. You cannot just stop taking prolia without another medication to lock it into your bones.
I started Fosamax (Alendronate) 5 months ago. So far the only problem I have is that I am more fatigued on the one day I take it, than the rest of the week. I have my next epidemiologist appointment in May so I will discuss my day of fatigue with her.
So far after 2 1/2 months doing well. April 10 th is a CTX so will know where osteoclasts are.
I have had that also. I’m hoping to get a different doctor and a new prescription, as 3 years and my T score hasn’t changed
That’s very disappointing, I will see my doc in May and have another scan… hoping I see improvement. I’m a bit nervous of trying a different prescription after reading some of the entries. Let me know what you go on and how you’re doing. Do you exercise?