Hello, I joined today to get help in deciding what medication to begin

Posted by luluz @luluz, Apr 12 4:43pm

Hello, I need help in deciding what medication to begin taking for osteoporosis. I’ve been prescribed Tymlos and the box warning for bone cancer is very concerning. Prolia was second option but that also has its drawbacks. I would appreciate hearing from people who are taking these medications and if they have experienced any serious side effects.

Interested in more discussions like this? Go to the Osteoporosis & Bone Health Support Group.

@windyshores

@dooshie I am doing Evenity after Tymlos. I had to convince my doc!

Also, in place of Fosamax, you can do Reclast infusions. I am going to do a low dose with lots of hydration and tylenol: 20% dose every 3-6 months.

Michael Lavacot is on Prolia I believe. A lot of us are avoiding that. Maybe he is just doing 2-3 shots which some docs are now saying means less rebound.

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@windyshores you are lucky you have a doctor who will agree to 20% reclast every 3 months or so. When are you doing that? I’ll be very interested in the outcome, as I may propose it to my endocrinologist after my two years on teriparatide is up!!! BTW, my first four days of injections have been side effect free🥳. Just a little redness around the injection site and burning eyes for an hour or so the first day. Even those minor ones are gone now!!!

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@lynn59

@windyshores you are lucky you have a doctor who will agree to 20% reclast every 3 months or so. When are you doing that? I’ll be very interested in the outcome, as I may propose it to my endocrinologist after my two years on teriparatide is up!!! BTW, my first four days of injections have been side effect free🥳. Just a little redness around the injection site and burning eyes for an hour or so the first day. Even those minor ones are gone now!!!

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@lynn59 great you are not having side effects and helpful to everyone who is scared!

My doctor did not "agree" to the lower dose of Reclast. He suggested it. I have heart and kidney issues that are relevant and am generally sensitive to meds.

During my cancer treatment, which caused bone loss, he did not prescribe the usual Reclast to go with the cancer meds, because at the time it was thought to aggravate afib (which I have once annually). Now I think the concern is my lower kidney function.

There may be no reason for folks to have a lower dose. It involves getting infusions more often. Many people tolerate Reclast quite casually, some have fluish symptoms. Whatever you do, hydrate and ask for a slower infusion.

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Thanks for the clarification @windyshores. I wrongly assumed you preferred to split it up. Personally, I would feel more comfortable not infusing a year’s worth at once, although that is probably because I’ve never done it, so I’m a little frightened. Just like I was scared to start teriparatide, which so far has been quite easy and tolerable.

It sounds like you have been through a lot, and I commend you on your attitude and your willingness to help us all through these uncertain times❤️

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@lynn59

Thanks for the clarification @windyshores. I wrongly assumed you preferred to split it up. Personally, I would feel more comfortable not infusing a year’s worth at once, although that is probably because I’ve never done it, so I’m a little frightened. Just like I was scared to start teriparatide, which so far has been quite easy and tolerable.

It sounds like you have been through a lot, and I commend you on your attitude and your willingness to help us all through these uncertain times❤️

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I do prefer splitting it up @lynn59. But I am grateful my doctor suggested it!

I have esophagus issues so Reclast is my only choice to lock in gains, and I figure doing low dose more frequently is almost like doing an oral med.

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A presentation that may be of interest:
https://calendar.app.google/oftZ14vey8y4SM886
Join BHOF Chief Medical Officer, Andrea Singer, MD and Cate Lockhart, PharmD, PhD, Executive Director of the Biologics and Biosimilars Collective Intelligence Consortium for an informative webinar about osteoporosis medication and treatment options. You will learn about weighing the associated benefits and risks of medications and gain insight into speaking with your healthcare practitioner about treatment planning and osteoporosis management. The differences between biologics and biosimilars will also be discussed.

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@gently

luluz, Tymlos is a very good choice. And I consider Prolia not good. Tymlos works by building new bone. Prolia works by preserving old bone. With Tymlos you get better bone.
You might ask your provider to order bone markers before your treatment begins and then at three months for the remainder of your treatment time. A fellow commenter wrote about being on Tymlos for two years without gaining bone. All these drugs work for some and not for others.
And some people have unwanted side effects. So keep posting. We have an astute poster who has clever ideas about avoiding those side effects.
I'm finishing a year on Forteo, a drug similar to Tymlos.

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How are you doing on Forteo? It’s the drug we are considering for my husband who has osteoporosis. He’s already had one compression fracture. His is from taking high doses of prednisone for over a year - he has PMR and GCA.

Also. Are you being told you’ll need to take another drug after stopping Forteo? From what I’ve read once you stop Forteo you lose bone at a fast rate if you don’t start a medication like Fosamax. Would love to hear what your doctor is recommending. And how long the plan is to keep you on Forteo and a follow-up drug.

Wishing you the best!

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@susanfalcon52

lulutz,
Welcome to this site. Most of the helpful info I find - I find here. There is a poster on here who I trust more than I trust my doctors. WS, you know wjo you are. 🙂
I have reported on my drug journey here many times and will do so again.
Disclaimer: everyone is different and reacts differently to these drugs.
I did five months of Forteo with no side effects. Later, five months of Tymlos with no side effects. Yesterday, I had my 11th set of Evenity injections. No side effects. In June, I go on Reclast. Fingers crossed.

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Could you please share your most trusted person here. I too am getting my best info here. 😊

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@gently

luluz, Tymlos is a very good choice. And I consider Prolia not good. Tymlos works by building new bone. Prolia works by preserving old bone. With Tymlos you get better bone.
You might ask your provider to order bone markers before your treatment begins and then at three months for the remainder of your treatment time. A fellow commenter wrote about being on Tymlos for two years without gaining bone. All these drugs work for some and not for others.
And some people have unwanted side effects. So keep posting. We have an astute poster who has clever ideas about avoiding those side effects.
I'm finishing a year on Forteo, a drug similar to Tymlos.

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One more thing. Who is the astute poster who can help with avoiding side effects? Thank you in advance.

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@susanfalcon52

lulutz,
Welcome to this site. Most of the helpful info I find - I find here. There is a poster on here who I trust more than I trust my doctors. WS, you know wjo you are. 🙂
I have reported on my drug journey here many times and will do so again.
Disclaimer: everyone is different and reacts differently to these drugs.
I did five months of Forteo with no side effects. Later, five months of Tymlos with no side effects. Yesterday, I had my 11th set of Evenity injections. No side effects. In June, I go on Reclast. Fingers crossed.

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Could you please explain why you went on Forteo followed by Tymlos followed by Evenity and going on Reclast.

We are at the deciding point on starting his first medication. He has a -3.4 thoracic spine result so we need to do something quickly. We’ve put off starting on Fosamax as his starting point. From what I’ve read here he needs something different first. All of this is so confusing.

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@isabelle7

How are you doing on Forteo? It’s the drug we are considering for my husband who has osteoporosis. He’s already had one compression fracture. His is from taking high doses of prednisone for over a year - he has PMR and GCA.

Also. Are you being told you’ll need to take another drug after stopping Forteo? From what I’ve read once you stop Forteo you lose bone at a fast rate if you don’t start a medication like Fosamax. Would love to hear what your doctor is recommending. And how long the plan is to keep you on Forteo and a follow-up drug.

Wishing you the best!

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Isabelle?, I'm so happy with Forteo that I'm having bone markers to see how long I can stay on the medication. I'll have a dxa 7/2 for find out if Forteo has been effective.
It seems to me the very best choice. Tymlos may have a slight advantage in bone gain, with a much higher dose of medication.
I am repeatedly advised to follow with Reclast. But if I follow with a bisphosphonate, it wiil be risidronate. I will be wanting to transition back to Forteo. But my plan is to take Forteo forever with short pharmaceutical breaks (two weeks I think).
Applauding your choice, I should caution that there can be adverse effects. Those generally diminish after the firs four hours and stop when the drug is completely eliminated at 24hrs.
wise choices, best luck

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