I took Duluxetine/Cymbalta for 3 mos. initially it was a miracle drug. It took away all my fibrobsymptoms but I couldn't tolerate the side effects. Did not allow me to sleep more than 3-4 hrs max per day (didn't allow me to nap either), persistent yawning, profuse sweating w/ physical exertion, night terrors, & occasional blurred vision. Dr said side effects would eventually dissipate but started to feel weird from sleep deprivation. When I decided I no longer wanted to take it, medication dosage was gradually decreased over time. The most noticeable withdrawal symptom was vertigo!

Currently, I am in Water Phys Therapy (significantly reduces pain), Flexeral & medical marijuana occasionally, CBD oil or edibles, recommended exercises for water & land, swim, bike & hike. Winter (cold temperatures) is harsh on body& Fibromyalgia flares up a lot (body aches likes flu, pronounced fuzzy brain b/c of intense pain, & fatigue. Remain wrapped in electric blanket & heating pads.

I was actually on plaquenil 12 years ago when first diagnosed with Bechet's disease and then I was diagnosed with fibro secondary, I was also on colchicine & was on so much meds, I stopped everything myself & only take what's needed for the symptoms as they arise, however I am now thinking of speaking to my doc and maybe starting back on the plaquenil. Hope you continue to feel relief. 😊

I am on .gabapentin and lexapro. I took the plaquenil for 3 years and didnt seem to help so we changed it. I also take tylenol extra strength in the morning and sometimes if needed in the afternoon. I also have tramadol but I dont take that on a regular basis unless i am having a flare

I was diagnosed with lupus , and also have fibro ,my Dr put me on plaquenil. It does help alot

https://en.wikipedia.org/wiki/Hydroxychloroquine it's a hard read, but my rheumatologist told me it does that.. seems to be pretty full on stuff..