Tymlos side effects I've encountered
Hi. I started Tymlos in February 2022 and about a month after starting it I began experiencing excruciating muscle spasms, esp in upper thighs and feet, neuropathy, as well as debilitating hip, leg, and back pain. My doctor wanted me to try and stay on it for at least a year, but I absolutely could not go on living with the pain I experienced. I stopped taking the Tymlos completely 6 days ago and all my symptoms have subsided. Has anyone else experienced these side effects while on Tymlos?
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@windyshoes,
Do you mean I should stop squeezing my skin while the needle is still in? I always have a bubble of medicine on the needle when I take it out. I asked the endo's nurse about the bubble and she said it was alright. I worry that I'm wasting medicine.
I let go of the skin as it is being injected to avoid medicine leaking. So pinching up allows the needle to go into the fat area, initially, but I let go simultaneously with the injection. I am so used to it because my kid has type 1 diabetes- 30 years of shots- and am realizing it is tricky for others!
Thanks so much @windyshores. For all of your help!
I was fortunate to get appt quickly to a Bone Health Specialist and get my meds from a Specialty Pharmacy who were great educators . Get a different Dr.
You were very fortunate to get a good doctor. Hoping I can find one too. Still looking
Hello dianestanley, I have just been diagnosed with osteoporosis in my 60s. This was so unexpected because I thought I was being careful and taking care of myself. My dr said that sometimes it's just genetics.
The reason I noticed your post is because I have a lot of issues with my teeth and jaw too.
I have not started on any osteoporosis medication since getting the diagnosis a week ago because I am scheduled to get a dental implant this month. I read that I will need a 6-9 months for the implant to completely heal so I am looking for bone building medications as an alternative to bone preserving medications like Fosamax. So I may be on a bone building medication like Forteo and Tymlos soon in order to take me through the 6-9 month period that my dental implant will need in order to heal.
It sounds as if you have a good oral surgeon. What I am finding is not all oral surgeons or drs are equal, some are better than others and that is the main reason people do better or don't.
That said, which oral surgeon are you using?
Also, do you have a bone doctor who treats you with the Evenity?
I am currently with a GYN doctor who diagnosed my osteoporosis but it would seem I need to find a bone doctor or an endocrinologist who understand parathyroid affecting drugs like Forteo and Tymlos and their effect on the body, how to take and monitor it.
I will travel cross country if I have to in order to make sure I have a good oral surgeon.
Another thing, I know this could happen to me soon because I am experiencing problems with my right hip. When you had your hip replacement did you have osteoporosis then?
Thank you so very much for any information.
@healthmatters without fractures, I have been told and read that osteoporosis does not have symptoms. Pain in your hip may be from osteoarthritis. Have you had an x-ray?
@lnl, I am on 4 clicks and plan to stay at this level. I am very sensitive to all medications and petite. I have been on Tymlos for 5 1/2 months and started at 2 clicks. I recently learned that I can't just buy the pens every 2 months. I started my third pen the other day and the side effects all came back on the same 4 clicks. I can tell that the medicine is so much stronger than what I was taking before, even though I always refrigerated it.
I am also learning that all 3 of the anabolics, Tymlos, Forteo and Evenity, appear to only help trabecular bone and make cortical bone porous. I broke my 2nd metatarsal in my foot. After 11 weeks it still has not healed on Tymlos. This is the 4th fracture in less than 2 years and all others have healed quickly. I wonder if the problem is the Tymlos. My endo wants me to keep taking it for my back (which has never fractured but has poor density according to my DEXA scan). My orthopedist suggested not taking it for a couple weeks to see if it helps. I am scared to do that. Does anyone know how soon you have to take a bisphosphonate after Tymlos?
I stopped Tymlos after 6 months last October. I couldn't take all the side effects. I never really got beyond 4 clicks (once or twice on 5). In that short time my spine numbers (trabecular) increased (spine was not the problem), and one hip increased and one hip decreased (cortical). To answer your question at the end: since the goal of the bisphosphonate is to "lock in" gains, the sooner you start on it the better. My endo told me I could/should start immediately, but I took a week or two just to give myself a moment without taking anything. I struggled a lot with Tymlos, got wonderful support from people on this site, but ultimately I couldn't do it. Also, my hair (not all) fell out. I just couldn't do it.
Thanks @lnl. I'm wondering if I can continue too. I will give it a week to see if the side effects improve. I can't take the biphosphonate pill, so would have to take the Reclast injection. @windyshores has suggested a low dose of that every 3 months.