I was just given vesicare by my neuro. Just looking for others experiences with it. What about any side effects?
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Vesicare anyone?
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I take Vesicare. The only side effect I've noticed has been a dry mouth. I have a dry mouth anyway without the Vesicare, but Vesicare makes it worse.
I use an oral moisturizing gel and a toothpaste that is supposed to help with mouth dryness.MEMBER OF MS WORLD SINCE 4/03.
SPMS diagnosed 1980. Avonex 2002-2005. Copaxone 6/4/07-5/15/10.
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didn't work for me
I was on Vesicare before I was diagnosed with MS... before it was even a consideration... didn't work for me. I can't even tell you know what meds I have been on for bladder issues, but right now 8 mg of Toviaz only helps.... I always wear a poise pad... been to the urologist and he was really no help. Once I started to pay attention to all the Vesicare comercials, it did not really meet my needs... I didn't have leaky pipes... but when I gotta go I gotta go... right then.
Good luck. I hope it works for you!!
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Took Vesicare before MS diagnosis after Detrol stopped working for night-time OAB. Vesicare worked well and actually helped "re-train" my bladder. I was able to stop the Vesicare and now I don't get up 10 or 12 times during the night - only 2 or 3. I would definitely take it again if I needed it and didn't have any noticeable side effects.
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