arava and anemia

About 1 week after stopping MTX, I stopped my folinic acid and my hair loss seems to be worse and also my nails are splitting and my tongue is sore. ( I also had 2 Remicaid infusions 2 months ago in August and 1 week of Arava in May and am on Plaquenil (past 4 months and for awhile in the past).

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.

I called the doctor last week and told him that I was feeling terrible on this Arava and that it was making me worse. He told me to stop taking the anti inflammatory with it and my stomach wouldn't hurt. i told him that it wasn't my stomach it was all over and they ignored me. I am so frustrated! he is the only rheumy doc that takes my insurance around here. I will give it a few more weeks and if it doesn't get better I will talk to him at my next appt on August 24th.

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.

Has anyone else taken this drug for arthritis? I started it several months ago and and seem to be getting a large amount of side affects.I have had upset stomachs with lots of reflux.When I exhale the air from my stomach it tastes horrible...like a decaying tooth.There is a horrible metallic smell consistantly with my stools.I have lost weight.I have constant tingling all over my body.I have had many headaches and low grade fevers.

Right now my doc is tring Cellcept. The jury is still out. But I have been on steroids, Plaquenil, Arava, Methotrexate and now Cellcept.

We had to wait 4 months of hell to be seen by a pyschiatrist and then had to wait about another 3 months to see some benefits from meds - clonidine and sulpiride. The tablets made him very tired and down and didnt go to school very often as he couldnt concentrate and fell asleep in class. He is very good at keeping in his vocal and motor tics when in public and with his friends but now he cannot do that. His motor and vocal tics are worse than ever.

I, too, have been on Arava for a month with nothing but worsening pain and symptoms. I have been told, as drbob992 said, that it can take quite some time to begin to help, if it is going to help. Usually, when it fails to help much or takes longer than "expected" a biologic will be added. You may want to discuss this with your rheumatologist. Aggressive treatment is needed to slow down progression of disease activity and erosion. I'll be starting one in January 2013.

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. Also, my bowel movements are mostly yellow soft to almost runny (sorry). My urine is bright yellow almost neon. Recently, my husbands ins plan changed and we have to pay a lot more now.

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 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.

}, at which time i started taking glucaphage. My np checked my b-12 level and it was low. since taking b-12 shot monthly and supplements sleep is a non issue. gulucaphage can cause b-12 defficiency in some people and i have complained about my legs tightening up at night and experiencing hand tremors. all symptoms gone after 1st b-12 injection. just wanted to let those of you on glucaphage know about a side-effect often overlooked.

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 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?

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.

A friend of mine has PA and has been taking Enbrel for years and she is in great health now. I started taking it 14 weeks ago after being so miserable for 4 years. I feel the best I have since getting sick 4 years ago. I urge you to speak to your Dr. about it. Take care.

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 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.

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 28years old female. i have anemia and recently i have been treated with hypothyroidsm. i am taking synthroid. the levels are in the normal range now. i have been anemic for last year or so but i never used to be fatigued. lately i am feeling very fatigued all the time with knee pain, etc.I am not sure whats going on. the doctor feels it anemia which is causing the fatigue but i dont think so. any ideas.

i asked her and she said she is negative and ive asked numerous times. she told me she has anemia and from what i understand that can be caused by hiv. if i tested negative at 100 days shall i still worry. the thing that concerns me alot is that i had a rash and weird flu like symtoms 6 weeks later. but at 100 days tested negative . please respond and be honest!

Hi beeama! I don't know what the instances of anemia and interferons are, but if you've not taken any supplements, and then go off the rebif for a week or two, then re-run the labs and they check out good you very well could be affected. It is the docs responsibility to order the labs, but have found too I have to remember to ask for the script for labs. Since it was 6 months ago - they should be run again for good measure.

Does anyone know if nexium can cause anemia? I have been on it 13 years and suddenly have iron deficiency anemia.

My brother is only 6 yrs old and he is sick for 1 month,the doctor check his blood and the result is low blood so they told me that i need to find a blood donor for my brother the next day i give blood..The doctors diagnose is ANEMIA WITH CHRONIC ILLNESS..so they give my brother blood 2x.. and the next laboratory in his blood is turn to normal.. Then the X-RAY result is CONSIDER RIGHT HILAR ADENOPHATHIES.. they gave me a request to the laboratory to do the ANA test to my brother...

He told me to take one a day but i been taking them for two days and i feel a little better and some has gone away but my hands and feet got very swollen and hurtful. i dont know what it is and its scaring me because I've never been the type of person that has allergic reactions?

m worried that the syncope may have been caused by a run of PVCs and not the anemia, and that level of anemia does not seem enough to me to cause a person to faint. She has previously been very healthy and active. I appreciate your input. Thank you.

Arava and anemia

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