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I began taking Plaquenil recently for my RA, because I can no longer take any drug that suppresses my immune system. (I had hystoplasmosis...almost died of liver failure as a result.)
I have regular visits to the optometrist scheduled as long as I'm taking the drug, because of the possible side effects...but I'm still concerned about the "visual disturbances" that can come as a result of the drug.
I know Plaquenil takes about 6 weeks to really begin working and I've only been taking it for about 2-1/2 weeks.
I guess I'm just wondering if anyone else out there has been taking the drug longer than I have, and might know a bit more about this visual side effect?
My doctor has been talking about putting me on Plaquenil for my Lupus. If you are still on it, could you let me know how well it's working, and how bad the side effects are? I'd appreciate it.
Hi Jazzfish, I am not on Plaquenil, but my best friend, who has RA, was on it for years before she switched to Embrel/Remicade type drugs. I will ask her about the visual disturbances and get back to you.. but, FYI, I can never remember her mentioning that, and she was on the medication for a long time (she was diagnosed at a very young age). Cheers, Stacy
I have been taking Plaquenil for lupus for about 5 years now and have had NO visual disturbances from the medication. I do get exams though and make sure my rheumatologist gets them. I guess it isn't a Rare side effect but it isn't real common either. Thank said, Plaquenil has been a life-saver for me. I would hold on to that medication for dear life!
