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Avonex liver problems

Common Questions and Answers about Avonex liver problems

avonex

439601 tn?1357860886 I would be very interested in hearing what you all find out about with there being a connection between the Avonex and gallbladder problems. As I mentioned earlier post, I am taking Copaxone, but it for some reason I have to stop taking it, Avonex would be my next choice for treatment. I happen to already have a gallbaldder issue that I'm treating with changing my diet rather than surgery unless it gets worse like yours did.
Avatar f tn Yes, I think you really need to report this to your neuro. Are you being monitored for liver problems since starting Avonex? That's always a good idea with this med, since the enzyme levels can get fouled up. I also get just the usual effects from Avonex (on it 4 months), but I've learned how to minimize them and so am doing very well thus far. Please talk to your doctor and let us know what you find out.
Avatar f tn It is a totally different drug than the others. There are no problems flu-like symptoms, depression or liver toxicity. It does take a good long while for your body to adjust to the copaxone and let it work. I was on it from October 2008 until Dec 2011 and did well initially. It wasn't until the last six months that I started having a few problems with being therapy compliant, but that is a story for another time. copaxone is a very good drug and I hope you do well with it.
462771 tn?1358355843 s imperative that I get it under control, so I was thinking about asking my neuro/PCP about stopping my Avonex for a few weeks to see if it goes away and my ASTs come back down again. No one ever told me what the procedure would be *if* my liver started having problems again, so is it safe to assume that they're going to recommend changing meds?
Avatar n tn ve been on Avonex for the past two months. The side effects have been minimal for me. My problem is now my liver enzymes are elevated. Dr. said I may have to try something else if my elevated liver enzymes continue. I don't like the idea of a daily shot with Copaxone, but I'm also concerned about the side effects of the oral medications. I won't consider Tysabri at this point because my MS diagnosis is fairly new and I want to try other treatments first.
Avatar n tn Have there been any studies published as to the possible long term effects of Avonex use? I am a 10 yr + user of Avonex and am becoming concerned. My healing time from minor cuts etc seems to be exceedingly long. I recently under went dental surgery and my dentist commented on my slow healing. I am at an age where major surgery occurs and fractures also some times and I am afraid that I would be debileated long term or worse if this was to occur. Any info would be greatly appreciated.
Avatar f tn I wondered why in the world Biogen would even make Plegridy, given that it has the same potential side effects as Avonex and other interferon meds---depression, flu-like symptoms and liver problems, basically. It seems the main differences are that it is a subcutaneous injection and thus not deep, and that it is used approximately half as often as Avonex. Will they drop Avonex? So now I'm wondering if anyone here has used Plegridy, and if so, how things are working.
1230912 tn?1273492770 I had my 1 month (after starting my DMD) blood test drawn on Friday and I know they are checking for liver problems, so when I got the results back I became alarmed. I just want to know if the alarms are warrented though? ALT was 70 - Standard Range 9-52 Lymphoctyes % 50.7 - Standard Range 21.8-41.6% Neutrophils % 39.8 - Standard Range 49.2-70.
Avatar f tn I am an MS patient and I have recently started taking Avonex, (I have had two injections so far) and I have been having problems sleeping.Does anyone know if Avonex causes insomnia, at all? I have read all the possible side effects Avonex may bring, but sleeplessness doesn't seem to be in the list.
Avatar f tn I also hope that he has been doing regular blood work testing to check your liver enzymes every six months, while being on Avonex. I think it's time to ask your Neuro to check you for the neutralizing antibodies now. I don't know the cost, but it IS a blood test.
Avatar f tn Given you say you have had liver issues in the past, you may not be a good candidate for the interferons. As others here have stated, fortunately Copaxone is an alternative that does not pose a risk to elevating your liver enzymes. Ensure your neurologist is aware you have had liver and thyroid issues in the past so together you can make a fully informed decision. Another consideration with the interferons is a history of depression.
Avatar n tn I have only heard of digestive problems.
233622 tn?1279334905 My jaw is too. I am going to be starting Avonex on Wednesday. Hopefully that will help get this under control!!
97654 tn?1214348650 Hi, I was recently diagnosed with MS and had my first Avonex injection Friday. Friday night was tough (fever, chills, pain and eventually heavy sweating) but I felt pretty good by Saturday morning. Saturday afternoon I started feeling kind of down and by Sunday morning I feel even more so. I can't decide if this is a result of the drug or just the situation as a whole.
649926 tn?1297657780 I was diagnosed in February of this year and was given a prescription for Avonex that day. I had to have a blood test to check my liver function and my AST and ALT levels were way high, and to make a long story short, they still haven't come back down to "normal" and I'm still not on Avonex. Apparently, liver function tests have to be done every 3 months for the first year on Avonex (or any interferon, for that matter), and they recommend 6 to 12 month intervals after that.
649926 tn?1297657780 Hi! I am sorry for all of you that are also suffering hair loss. As if we don't have enough to deal with! My family thought that I was making a big deal out of nothing until I washed my hair and ran my hands through and came away with a full hand of hair. We are not talking your usual hair loss here!
387113 tn?1313512083 m thinking of starting Copaxone cuz little to no side effects and its not metabolized through your liver. But, does it slow the progression of the disease like Avonex? Im a full time RN student and working in the ER this summer so I dont want flu like symptoms stopping me and I dont want to damage my liver. What do you guys think?? Thanks!
Avatar n tn I have been on Avonex for 10 years. I am feeling pretty good. Very few ms problems. My gait is somewhat labored, I have intention tremor in my hands and some numbness on my left side. I am considering stopping my Avonex becausse of the cost. Have not seen my neurologist yet but want another persons opinion also.
1142230 tn?1268675666 Back in 2002 I had my first less severe episode of numbness from waist down with residual problems in both feet. Urinary and incontinence for about 10 years, other problems with fatigue, depression, anxiety, cramping in legs and feet, dystonia in right hand, dx with Epstein Barr syndrome back in 90's, hypothyroidism since early 2000's, on Synthroid. The neurologist diagnosed me with MS on Jan 5, 2010. He wants to put me on Avonex ASAP.