I'm not completely pain free, but it's a lot better than it was. I've been on plaquenil since mid June I have had a lot of stress in my life so I can't determine what is causing what. Not seeing any improvements with pain but I just went to 0 prednisone 3 weeks ago. said give it a few months and if I don't see any improvement I might as well go off of it. Wanted to let you know that I was on plaquenil for about three years and I told my RA doctor that my fatigue was worse. It just seems like the fatigue is worse than it has ever been, and it doesn't seem to matter if I go to bed early or take a nap during the day. Woke up and cleaned the kitchen an hour later(my kitchen is a galley kitchen 8 ft maybe.no time) Took a nap. Early on I did get those stomach cramps and diarrhea. All my pain is tolerable and he sees no deformities so he says he doesn't see RA activity. Just because the pain is tolerable doesn't make me like it any better. He did a plaquenil test and sure enough it was low. Hydroxychloroquine lupus life insurance Plaquenil empty stomach Plaquenil abbreviation I started on Plaquenil again. I stopped taking it the first time because my stomach hurt so bad. My rheumy said to just take a half a pill right now 100 mg. It's been about a week now and I am noticing dizziness, fatigue and just kind of weak. Can this be a side effect of Plaquenil when you first start? I don't recall it happening last time. The causes of fatigue in Sjogren’s syndrome are numerous. The only strong therapeutic recommendation for fatigue in Sjogren’s syndrome is exercise. Hydroxychloroquine is the most widely prescribed treatment in the U. S. to manage fatigue in Sjogren’s syndrome, but this practice is largely made based on clinical experience. Sjogren's SHOW-grins syndrome is a disorder of your immune system identified by its two most common symptoms — dry eyes and a dry mouth. The condition often accompanies other immune system disorders, such as rheumatoid arthritis and lupus. I wake up tired in the morning, get my kids fed and off to the schoolbus, and some days that's all I can do until it's time to go pick them up and make dinner, then I collapse after the kids are put to bed. I don't know if this is just the way RA is, or if it is a side effect of the medicine. Wasn't going to eat luch because I would have to move to do it.husband bought out. Kids came home, helped with homewrok, made dinner..picked up couch(because my blanket and pillow were there) Went to bed at 9. Plaquenil sjogren's fatigue Plaquenil - General - Sjogren's Syndrome Support, New Sjogren's Guidelines Outline 19 Treatment Recommendations. Plaquenil 200 mg tablet adalah Jun 11, 2013 For many patients with Sjogren's, Plaquenil hydroxychloroquine has long been the go to drug that their doctors prescribe. It is often the first line of attack before other more aggressive therapies are added such as methotrexate or rituximab that have bigger impacts on the immune system. Study Raises Questions about Sjogren's and Plaquenil. Sjogren's syndrome - Symptoms and causes - Mayo Clinic. Sjogren's syndrome - Diagnosis and treatment - Mayo Clinic. Rheumy started me on plaquenil and it helped with the tiredness and no energy for a while but it did not do anything for dry eyes/saliva at all so why take it. It is supposed to slow down the immune system so your problems aren't as bad.i.e. tears/saliva. But, I started getting bronchitis in Jan-April. I was diagnosed with Sjogrens Syndrome 3 months ago. I also have rheumatoid Arthritis and Hashimotos. My rheumatologist prescribed Plaquenil in hopes to control all 3 conditions. I would say that Plaquenil has basically given me my life back. I suffer from debilitating joint pain, fatigue, brain fog and extreme anxiety. I was diagnosed with Sjogren’s a year ago Early Sjogren’s Panel by the doctor I see for Ehlers-Danlos Syndrome. I started at a very low dose- 100mg per day 1/2 of a 200 mg tablet, in addition to a small dose of modafinil I was taking for fatigue, which is my worst symptom. I don’t have joint pain knock on wood, also unusual for EDS. After a couple of months I was feeling so much.