arava liver damage

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.

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.

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 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 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.

I am so scared I have caused damage to my liver. After I get off of these will it repair itself or am I in trouble. The only syntom I have right now is welling in my akiles and feet. But i have taken fluid pills for the fluid for yrs before I started taken lorcet.

The recommended dose of paracetamol for a single adult is two standard 500 mg tablets. Researches have reported that the threshold for liver damage to start from a single paracetamol overdose is 15 gms (30 tablets). However liver damage could start to occur at a single overdose of 24 standard tablets or 150 mg/kg body weight, (whichever is the smaller).

(Former drug user) what are the chances I already have liver damage??? I go in the morning for a liver scan to check and I am nervous to know!!!

Is it possible to cause liver damage from a few years of pain med abuse? Damage severe enough to cause stomach pains?

I have been taking Darvocet for about two years now. I began just taking one a week at night after a bad day and it has progressed to 1-3 daily for about 6 months now. I went to the Dr. for a checkup yesterday and the ALT liver function test was high. The other liver tests were normal just that one was high. The Dr. thinks it is from my acid reflux medication and is changing that but I rarely take it. Could it be the Darvocet?

from the doc forum: http://www.medhelp.

Can anyone tell me what it's called when you have liver damage from medications

The only way to truly ease your mind is by being totally honest with him/her. I have liver damage and kidney damage due to drugs stage 2 liver stage 3 kidney.. if your liver were damaged and you had a flare your belly would be extended/pain upper right you would be lethargic/vomiting.. other symptoms but these being severe.. It is not fun and I would not wish it on anyone.. I contracted hep C from slamming and further continued the damage through pills/alcohol..

I have never been to hospital, I dont appear to have yellowing of the skin or eyes. What is the likly hood of damage to my liver, and if stoped now could my liver possibly recover from and damege.

Hard to say but if he stops attacking the liver with alcohol, no further damage should be done and some of those numbers should go down at least a little.

My brother has been in the hospital for 12 days for liver damage. His skin and eyes are yellow, abdomen pain and swelling of the stomach. They drained off 12 liters of fluid from stomach area. He's has dementia, no communicating with him that makes any sense. In this situation what is his chance to make it through this? The doctors and nurses are not saying much, but wait and see.

week 24 bloodwork showed virus undetectable [good news] my question is,the biopsy shows fatty liver and stage 3 liver damage. if the svr continues, will my liver heal itself? does this stage of damage cause fatigue. i know the peg/copeg can cause fatigue im just wondering if after i stop tx will my energy level improve? if anybodys got any 411 on this id sure like to know. thanx.

what causes liver damage ? is it HBV or our immune systems ? as well what is the cause of liver cancer and HCC?

Should I be worried that I have liver damage that is just not showing up? I have changed my diet significantly ( no dairy or gluten) but I am still very bloated. I am sick with worry that I have caused permanent damage. I am still very young, 28. What are ur thoughts?

I am trying to get her to have her lithium levels checked but she thinks she is fine (part of the disease), she is not sleeping well and not resting, physically pushing herself which makes swelling and pain from RA worse (had to stop Enbrel, Arava and Methotrexate to begin chemo). Still using patch and morphine tabs for pain, ambien for sleep and there are more meds.

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?

Just thinking,,,if a person is a stage 2 with moderate damage and does one full treatment and relapses,would the liver have reversed back to at least a stage 1?...also with this liver improvement,wouldnt the next round of treatment make it more sucessful...starting as a stage one now as appossed to stage two at the orginal start? i know there are chances of viral mutations and all that ,but all these things aside...i think this is positive news to the re-treater....ANY THOUGHTS?

Arava liver damage

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