arava rheumatoid

I have an Auto Immune Disorder of the connective tissue as labeled by my Rheumatologist. I take Plaquenil 200mg, and Arava 20mg daily. I have been on the Plaquenil for over a year and the Arava for 5-6 months. I am still having flares and experiencing pain on a daily basis. I'm a 28 year old male. My tested positive for ANA but the doctor hasn't labeled me with Lupus. I see my Rheumatologist on the 18th of December and I'm looking for the next step in my treatment.

I was dagnosed with rheumatoid arthritis and was put on Plaquinil 200 mgs bid. My pain hasnt been relieved totally with this med and the rheumatologist wants me to start on Arava in combination. Im scared of the hep c coming back with both of these meds. Opinions needed.

Thanks. I HATE drug side effects stories. My elderly mom's hgb dropped to 8.5 on Arava (for rheumatoid arthritis), I had a personality change on Ambien (so bubbly I couldn't even stand myself). We have to really be on the watch every time we add a new medication. I worry the most about people who require multiple meds. Think I will start taking B-12. Thanks again.

Just recently my Dr put me on methotrexate injections and arava after which my symtoms got worse.I went back to the RA DR and now she thinks I have Polymyalgia Rheumatica.Right now I'm in the processs of finding a second opinion. They say the symtoms of Polymyalgia can come on rapidly like the symtoms you discribe.

Under my ribs and almost on the side. I was taking a lot of Rheumatoid medication due to my doctors thing I had RA. My liver levels were elevated and I had this same pain then. I had a sonogram and a Hida scan (sp?) They told me I had Fatty Liver, to lose weight and to stop taking my Arava. I did and levels went back down. This was maybe a year ago. Now it is back and it sometimes it makes me sick to my stomach and I have a lot of gas.

As part of the rheumatoid process, firm, non-tender, subcutaneous nodules develop in about 25 percent of rheumatoid arthritis patients. These are commonly found at pressure points like the elbow, back of the forearm, and metacarpophalangeal joint. Nodules usually occur in chronic active cases of rheumatoid arthritis, and are commonly associated with more joint deformity and serious extra-articular manifestations including lungs, eyes, and blood vessels.

Hello, I am a 51 year old Caucasian female with rheumatoid arthritis and fibromyalgia. How long after stopping methotrexate (MTX), should I continue folinic acid (Leukovorin)? I was on methotrexate for ~1 1/2 years (last 6 month at 20 mg/ week). I had hair fall, then finally frank alopecia and discontinued the MTX one month ago. During the last month of treatment, I asked that my folic acid be changed to folinic acid (Leukovorin).

I started out on plaquenil but have added methotraxate low dose prednisone and arava to the mix.. My knees still feel like rubber and in the evenings i head to bed early. But it is helping with the pain dring the day. I just pray that the disease will eventually burn it self out.

I recently started taking Arava for my rheumatoid arthritis. My dr. added this to the Methotrexate and Prednisone I am already taking because I really wasn't getting much relief. Now I am getting a read rash behind my knees, ankles and calfs. has this happened to anyone else? Also, occasional bruises to my stomach area.

0) I was wondering if anyone here has taken Arava (Leflunomide) and their side effects? I started it almost 3 weeks ago for the RA and Sjogrens and have started to have nausea, hair loss, skin sensitivity, burning or tingling of skin, and restless legs (already had, but much worse now), vivid dreams, and torso pain like a cramping sensation in back and sides. I have read too much bad stuff about this medicine and I am hoping someone has had a good experience with it.

i take the leflunomide (arava) but also take pills for the reflux, which does help. I take renitidine i believe it is called. I found it worked pretty good for the swelling myself. I am also on the Embrel, but still do not have R.A under control. I just wanted to say that the arava was the best drug i have taken up until i was put on the embrel. I live in B.

She suffers from bipolar disorder as well as rheumatoid arthritis. She has taken lithium for 30 years, plus prozac with great results and no problems with mood swings. We began noticing mania symptoms about 3 days after beginning first treatment ( Folfuri 46 hours on take home infusion pump). That was almost 3 wks ago. Had her 2nd tx 4 days ago.

Prior to that she was on Arava for five months and it almost killed her. She lost 60 lbs, had heart issues, urinary tract infections, had no appetite and was incredibly weak. Her RA doctor said it was not the Arava. It was. I took her to the Lahey Cllinic and they confirmed it. I had taken her off the medication before going to the Lahey Clinic but it was a binding med. so it stayed in her system for months afterwards.

Hi, I was recently diagnosed with psoriactic arthritis and the doctor put me on Arava. I've been on it for 4 weeks with no relief. In fact, the pain has increased in all of my joints and my toes have decided to join in on the fun as well. My question is has anyone had any experience with this drug in the amount of time it takes to start working? Is it usually immediate or does it take time to "build up" in your system before it begins to work?

I know I have all the symptoms and do get worse when I am off of my Arava but I also wonder if I could have Lupus because I have a lot of the symptoms of it and my sister has it. My mother has fibro so I wonder if maybe that is what I have instead as well. Things are continuing to get get worse and my dr is wanting to start injection therapy for my symptoms. I just want to be sure I have ra before I begin these injections they really scare me!

My father has severe rheumatiod arthritis. He has been on a combination of Arava 20 mg ( Hydroxychloroquine) and Plaquenil (Leflunomide) . He has been going severly downhill since January and has lost 40 pounds, has constant mucous drainage that he chokes on especially after meals, and has severe shortness of breath. Can these symptoms be a result of the medications he is taking? Is it safe for him to take two synthetic DMARDS at the same time?

Have you tried xenazine ( chemical name is tetrabenazine)? We've also found clonex gives some relief.

are you on any other medications? i was also on arava when i started the humira and got a terrible rash on my hands and feet. i stopped the arava, took cholestyramine to get it out of my system. rash went away. still taking humira. no more rash, so that's good, but i'm not sure where these twitches are coming from. they started about three weeks ago. i'm so sorry you've been having this reaction. sounds like you've had quite a history. i wish you the best. hang in there.

I do get the cramoing sometimes for a day or two after the enjection. With the embrel the cramps do go away. I also take arava so maybe the combination of the drugs. Hope it it gets better.

Examples would include Methotrexate, Imuran, Arava and Plaquenil. Another approach you may want to try is to have the doctor add a medication to protect her stomach and keep her on the Lefora since it is controlling her arthritis.

Hi Jen I am 23 and was DX with PA beginning last year. Probably had it since 17 cause that is when my back pain first started. I am currently on Arava. Methotrexate didn't work, was on it for a year. Worked fine in small joints like my fingers but did nothing about my back. I don't think the Arava is working either. Doctor wants to start Humira end of the year. My diet doesn't make the pain better, certain things does make it worst though like alcohol.

Hi this is my second year of retuximab my infusion is due next week it has helped me so much i have tried endless drugs for my RA and the retuximab helps the most a few weeks after the infusion my blood result was normal i cant speak for everyone just my own experience i allso take methotrexate.

I am on Cellcept 2000 mg a day and I have noticed a that it has worked better than Plaquenil, Arava, Methotrexate did. How long have you been diagnosed and without meds?

i am 22 years old..i have RA(still desease) from about 10 years, i have tried almost everything..metothrexate(didn't well work),arava(had a baaad effect on me!!),remicade(no improvement),humira(had it about 4 times but had lots of problems with purshasing it and without good effects also),and i had also a both replacement surgeries for my hips ..

My RA factor was 20 last year. What is the normal range for the rheumatoid factor? This discussion is related to <a href='http://www.medhelp.org/posts/show/227148'>rheumatoid factor</a>.

Arava rheumatoid

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