avonex thyroid

Is anyone on avonex? My dr. wants to switch me to avonex, but with having lupus, I really don't want to go on an interferon. I'm on copaxone, now but because I have large welts on my arms he wants to switch me. I don't want to switch. Do I have the right to deny a new medication I feel would be detrimental to me?

t find much about this as a side effect on-line) or am I in that lucky 4% of Avonex users who have hair loss. If it is the Avonex, will it stop as my body gets used to the drug? Good God I hope so! Any insight is appreciated, as this is really stressing me out.....which can also cause hair loss!!!

The pharmacy questioned the large increase and called him to verify the dosgage he confirmed. He also raised my other thyroid medication from 30mcg of Armour Thyroid to 20 mcg of Liothyroxine because they are not producing Armour Thyroid any longer. I have been on this new dosage for a month and a half. I have been noticing my heart racing, skipping a beat, hot, sweaty, gittery. I went in to see the prescribing Dr. this morning and told him all of this and he said he over dosed me. Ok.

The last time I had bloodwork done on my thyroid function, all was fine except T3 uptake was 3 pts. below the normal low range (mine is 21.3 & reference is 24.3 - 39.0). Is this something I should have checked/should I go to an endocrinologist? I'm also wondering if the Avonex i'm on could be hurting my thyroid. This bloodwork was done a yr. after my starting on Avonex. I'm just curious. I'm fine with just leaving it alone. Thank you!

As I wrote before, I did fairly well with my first Avonex injection on Monday, had some side effects, took it easy on Tuesday, then felt well enough to run some errands on Wednesday. However, by Wed. night, my thigh kind of burned like I'd worked out real hard, and my radicular pain started acting up in the other leg, then proceeded to wrap around the top of my thigh like it's done in the past.

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!

You do not have to worry about avonex it does not suppress the immune system. Do not worry about the JC virus unless you are on Tysabri which you are not. To be completely clear unless your Doctor tells you otherwise you have nothing to worry about you are on a safe drug.

I read in there something about the thyroid and the effects of particular medicine on the thyroid and made my decision. I've not regretted the decision I made, so I'm glad I did so much research.

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.

Sigh, I have a question from a friend. She would like to know if avonex causes calcium deficiency? She is diagnosed with ms. Not like me.

Flu-like symptoms are a fairly common side effect during the initial weeks of Avonex treatment. It is recommended that you take your Avonex injection before bedtime. Immediately before your injection, and for the 24 hours that follow the injection, patients have found that use of over the counter pain and fever reducing medications can help with this common side effect." You could also get on the Avonex website for further info. good luck. hope that you feel better soon.

I have been on copaxone for little over a year its not working for me so my neuro has asked me to try avonex. My avonex nurse is coming this evening but I am wondering how long you actually gave it to get the symptoms of the shot to calm down. I am crossing everything to hope I dont get the flu symptoms so bad but we will see. I have a husband that works away and 3 small kids to care for, I dont want to be in bed all weekend when its the only time we get to spend as a family.

Hi guys, has anyone not heard from the AVONEX people once they were put on it.??? I have heard from heath nurses, and today, got my WELCOME package, but still no product. I don't know what is going on, and of course the lady or the rep from Avonex is away on holidays till the 2nd. of Dec..... so, I guess we will do it next week ... Just to let you guys know, they stopped my antiobiotic IV today, and said that it was an MS attack. Wherever there are nerves, MS can strike.

Hi Candy, When I was on the Avonex I had terrible itchy skin. I would start scratching and I would well up from the scratching. I also found that it dried out my skin as well. I use pure coconut oil right out of the shower then gold bond lotion right over the top of the oil. It seems to be helping tremendously. The oil soaks in quickly and the lotions seems to seal in the moisture. I hope this helps. Sorry you have this to deal with on top of everything else.

//www.themcfox.com/multiple-sclerosis/ms-drugs/avonex/avonex-blood-counts.htm updated 2004, it might be worth finding out if your having a negative reaction and need to change DMD.

I've been on Avonex for 2.5 years and it's suited me well but I have just had a 4 week break. I then took my injection on Tuesday night and was strangely fine on Wednesday and Thursday but on Friday, Saturday and today I have lost about 50% of my strength from my left arm and leg. Is this likely to be a side effect from restarting the Avonex (muscle weakness) or a relapse?

After being on Avonex for 1 1/2 years I have developed new side effects?? Red eyes with severe pain (in my eyes & behind my eyes) It started several months ago and now happens with each weekly injection. Has anyone here had to discontinue Avonex due to side effects?

DX on 2/14...started Avonex last week with nurse helping and did fine. This week I thought I did okay but noticed the plunger did not go completely down. It was the 1/2 dose. Since I am inclined to over analyze, trying not to panic. Figure I'll be taking more next week...but since you all seem like you know your stuff...thought I'd ask the experts. Thanks.

Hi, I was wondering if anyone who has taken both Avonex and Rebif could give some input here. I have been taking Rebif since this past June, but have started to wonder about how Avonex would compare side-effect-wise. As they are both interferons, I would think they would be similar, but I'm not certain. The idea of once a week sounds nice in comparion though, so I would like some actual first-hand knowledge. Thanks!

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.

I have been taking the Avonex shot for a few months now and have become accustomed to the effects of it. However tonight I have taken my shot and now I am having a tingeliing sensation going on. It's in my arm (R), both legs and also my abdomen. I know what to look for medically to be concerned but no where have I seen this as a side effect. Has anyone else experenced this?

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