Hi,
I been taking meloxicam for over 4 months on a daily base. I am worry that I will have long term side affects. Does anyone out there take it for long term and if so how long? Please let me know . Thank you so much!
Jen
Hi,
I been taking meloxicam for over 4 months on a daily base. I am worry that I will have long term side affects. Does anyone out there take it for long term and if so how long? Please let me know . Thank you so much!
Jen
Are you on anything else for your RA, or is that all you have been offered? Generally even tho' the DMARD drugs sound scary, they are a better long term choice.
For some people, even on DMARDS, there is no choice but to take anti-inflammatorys all the time. It's better not to, but life sometimes doesn't follow best practice guidelines. I hope you have also got a stomach protector or PPI to take alongside to look after your stomach lining.
Hi helixhelix ,
Currently I am taking mtx and I think it is not working. Hopefully my RA will find the right cocktail 🍸 for me. I called my RA to ask them about PPI meds but they told me only if I feel side affect from the meds then they will prescribe something. Thank for information.
I assume the goal is to feel better without taking any kind of pain meds daily. If anyone have positive outcome please share.....thank for your response!
It’s hard on your stomach. My doctor took me off because I have heartburn problems and she said no more meloxicam.
I found meloxicam gave me awful indigestion and reflux so I’m on Brufen Retard 1600mg. I do take omeprazole stomach protector. I’m on 15mg oral Mxt too. Sadly the Mxt has never really worked properly so I have taken these extra anti inflammatories fir 3 years. I’m about to try biologics hopefully. Just going thru the tests.
I'm a bit surprised by the response from your rheumy team. I was asked every time whether I was taking something to protect my stomach when I was taking meloxicam regularly (I only need to take it now when I'm coming off a raised dose of prednisolone).
I hope you are doing ok!! The remicade is in my body I’ve had 4 infusions. I really don’t know if it’s working but no flare ups lately. I do have pain but I don’t know if it’s the RD or damage caused by it. All the know is I’m not the same