Experiences with

Reclast

Now I am supposed to get an infusion of reclast. Has anyone taken any medicine for osteoporosis and what was your experience? Bonus points if anyone is on reclast. I have never drank milk and try to limit any steroids I night need.

Had my first Reclast infusion today. About halfway through my BP dropped and I was shaking so bad I almost levitated out of the chair. We stopped and I will see the endocrinologist next month. Has anyone else had these symptoms? Will I be able to get Evenity? Really freaky

Torn between trying natural remedies or taking Reclast. I broke my hip from a bad fall almost 5 years ago. Am now wondering if the OP caused it. Any advice?

My mom suffered an L1 fracture 5 years ago, was diagnosed with osteoporosis and put on Reclast injections for 4 years . Her levels were good so they stopped it. After a year, T12 fracture (kyphoplasty surgery scheduled next week) Now they are suggesting 1 of 3 options -- Forteo, Prolia, or Evenity.

After disappointing results on a second bone density scan a year ago, I decided to go with an infusion of Zoledronic Acid (Reclast) 5 mg/100 mL 5 MG/100ML injection. Because I was working to treat a Vit D. deficiency, I didn't have the infusion until August 6.

Had CTX done so I can start Reclast. CTX is 89. Has ANYONE had Reclast going in with a score of 89?

Now I have to take reclast and that is very scary. After 9 years of dealing with this,and many fractures, I am very tired of it all. How much can a person take🫨 Sorry for the rant

My Endocrinologist recommended Reclast IV. I’ve hesitated to take Bisphosphonates because of the side effects. Has anyone used Reclast after Evenity or Forteo ( in used 2016-2018). I also used Prolia from 2019 - 2023. I’m in the USA.

I have osteoporosis (worst is lumbar spine -2.5) and am currently on a drug holiday from Reclast IV after taking it for 3 years.

On Nov 7, 2024 I had a one hour reclast infusion. Because my body often responds negatively to medications, the Dr. decided it would be best for me to do a very slow infusion. Generally they are 15-20 min. infusions. There weren't any problems with the actual infusion.

I previously was on Prolia 5 years and then Reclast infusions two more years and then two years on zero bone drugs to present.

I have been on Reclast for 3 years. About a year and a half ago I was told by my dentist I have bone loss in my jaw. After researching Reclast I realized that it could be what's causing the bone loss in my jaw.

Doctor says it’s nothing to do with reclast but wondering if anyone else has had anything similar. I’m contemplating skipping 2nd infusion to see if pain goes away. They did X-rays to make sure no fractures and did not see any.

My issue I is that I had polio and si have post polio syndrome which makes me susceptible to muscle effects and aching anyway - an on reclast due to ADT aggravated osteoporosis and my paralysis and wheelchair use make exercise and definitely weight bearing more or less out of the picture.

Prolia… reclast… there seems to be controversy in taking the supplement… I thought I post here to get your feedback. I truly do not want to take any more medication. I was hoping that this would help in some degree

My endocrinologist recommends Evinity once/ month for 12months followed by Reclast for two years. She says I can then stop all drug treatment. I prefer not to use drugs but my doctor won’t offer any other treatment.

Is anyone taking this, and if so, what is your experience. Would you take this over Actonel or other biophosphate, and if so, why? My Rheumatologist is suggesting this for -2.5 T score of femoral neck. Thank you for sharing your knowledge

Has anyone with ET received a Reclast infusion for osteoporosis? My endocrinologist recommended it as my lifestyle is good but my T scores continue to get worse.

Are the other biphsphonates the same as Actonel in side effects, eg. if one causes migraine will Fosamax, Boniva or Reclast cause migraine? Thanks

Is the Reclast (Zolendranate) yearly injection better on migraine? I have just been told the Strontium Ranelate (UK) will not be available until 2025. I am running out of options, meanwhile losing all the bone made on Evenity.