Hello everyone. I have a question that I hope I can get answers to. I’m 28, was diagnosed with Relapsing remitting MS October 2015. My main symptoms are he MS hug on my upper right side and urinary retention. I am currently taking Ocybutinin for urunary retention, 5mg 3x a day. My question is wether there are any long term effects of taking this medication. I find that if I don’t take it it makes it a lot difficult to go pee. Would it be wise to try other options? I’m the long run will this affect me? Thanks for the help in advance.
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