Arava humira
Common Questions and Answers about Arava humira
arava
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 took my first Humira shot in my leg on Monday and last night my leg began to hurt really bad. It is a pain that is hard to describe. I told my husband it was a "bone pain" it hurts down deep in the bone from my knee to my hip joint. Today it is hurting mostly in my hip joint.I take darvocet daily for pain and it really isn't helping and neither is naproxen. Is this normal after the first few days of the injection?
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?
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.
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 ..
Also, I forgot to ask this at her last rheumy appt, but how is Remicade any better than Enbrel or Humira? (SHe hasn't been on them, but I just wondered why he chose Remicade.) Any info you can provide would be most appreciated! My daughter is at the end of her rope.
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.
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.
Anyone taking humira and feel like they are sick coming down with a cold for a week after injection? Not a full blown cold but the start of one. I feel like this always and this is my 3rd dosage ( counting the starter kit), so I'm new to humira. I've noticed if I'm stressed, I'll even get a sore throat. I know humira suppresses your immune system but are you supposed to feel like you're coming down with something every injection or will this go away with time?
Of course it seems a lot of folks have the same questions you do after reading humira info online - found a lot of questions asking if humira causes herpes.
If you already have herpes simplex, either orally or genitally, it could cause it to reactivate. Most people never get tested for herpes to know that they have it.
Hi monicaroni, I have been taking Humira almost 8 months. I take humira for Crohns Althougth reap the benefit for the AS. I am thinking that you probably had a concurrent infection brewing when you Started Humira. Good Luck managing your AS, I appreciate how difficult it can be with mobility issues, and treating pain.
As you well know Humira is an immuno-suppressive
drug , which mainly inhibits TNF (tumor necrosis factor).
There's a growing amount of evidence of the development of Autoimmune conditions, related to TNF inhibitors, such as Remicade, Humira and other biologics.
My husband missed his dose of Humira by 24 hours a week ago. He is now vomiting regularly like he did prior to his diagnosis. Is this normal with a missed dose? He has been on Humira since September.
I just started Humira (2 shots so far) and have had a worsening of symptoms since the first shot. My hands/feet have become swollen and my joints hurt more than before I started taking the Humira. I also have systemic vasculitis (Churg-Strauss Syndrome) and am on Cytoxan and Prednisone, but I have been taking both for more than a year and know the side-effects from each.
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!
Any body else taking humira? I have Ulcerative colitis and thats the meds they put me on. My condition is pretty bad because all three of my doctors told me not to come off the meds. That it could cause problems and early delivery. Any one?
Hola, lobo.... No tengo ninguna experiencia ni conocimiento sobre humira... he leído ahora que son unas inyecciones para tratar la artrosis, es para eso para lo que te lo han recetado ? Llama a tu médico y consulta con él/ella o la enfermera si es normal que te siga doliendo.. cuanto antes lo consultes mejor y es normal que les llame para algo así. Si hay una reacción, lo sabrán y si es normal te tranquilizará que te lo digan.
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