Hi all, just wondered if anyone else pours sweat with meds for fm. I was recently put on 30mg duloxetine (always think im talking about paint) then upped to 60mg and the sweating was unbelievable. At night I had to put a cold wet facecloth on my head to cool down. Sweats are always from shoulders up. Also felt very dizzy but was reluctant to stop it cos it helped so much with pain. Reduced dulox to 30mg and went back on reduced dose of citalopram 10mg and it's bit better. I also take 30 mg of MST continus a day. The sweating is still there. Any ideas on coping with sweats. Was diagnosed 17 years ago with fm,have asthma and the seemingly inevitable ibs. Also have myasthenia gravis affecting my right eye. Sorry this sounds like a right moaning session. Im aware many of you have so much more to cope with so am sending you all good wishes and gentle hugs. Ell
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