avonex website

When I clicked on the “coupon” for Avonex it simply routed me to the Avonex website, where they offer the first month of treatment for free, as they’ve done for a while. Don’t know how that program works, but I think you’re just best off for now calling Avonex and exploring your options. I didn’t see the bit about how vials are priced lower. (I presume vials is the medicine you mix yourself.

An MSWorld user "zeldaz" lost her Avogrip, a plastic piece that clips to an Avonex syringe and makes it easier to handle. Apparently they are no longer available from Biogen. The draconian forum admins there deleted offers to send "zeldaz" a new, unopened one. If "zeldaz" sticks her nose in here, send me a PM.

s 3 months prior to becoming pregnant but I am not too sure what you should do in your case. I have copied the following right from the AVONEX website: Pregnancy Category C: The reproductive toxicity of AVONEX® has not been studied in animals or humans. In pregnant monkeys given AVONEX® at 100 times the recommended weekly human dose (based upon a body surface area comparison), no teratogenic or other adverse effects on fetal development were observed.

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!!!

I am new to the website, and new to Capaxone. My question is what side effects does any one have to this stuff. Injection site is to be expected but the general body feeling. It is driving me nuts. I appreciate any remarks and comments.

I was wondering if anyone new a website where I could go and see comparisons in the different MS drugs, Avonex, Copaxone, Rebif,and Betaseron. I am interested in the success, side effects and anything that would be beneficial in helping us to decide which drug to choose.

I was dx 08 with RRMS which is quickly changing after being actively on Avonex since dx. The problem is MRI's are changing -turning into what my neuro thinks is Progressive MS. He said the lesions although not growing, are actively increasing in number (from 6 to 8 in 11 months) also with my reflexes, memory,ability to walk etc, etc, has worsened 4 fold.

s known that some people on the Interferons, Avonex and Rebif have had no additional lesions, that have lasted years. That was my experience when I took Avonex. Since I now take Copaxone and have only been on it for a little over a year, I cannot give you a personal view of how well the drug is working for me. I am beginning to notice less relapses, though. How DMD's work is not fully understood.

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.

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?

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?

Hello! I've just been diagnosed with MS and am wondering which drug is better. I've read the material for Copaxone, Rebif, Avonex, and Betaseron. I've narrowed it down to two -- Rebif or Copaxone based mainly on side effects. Which drug is the best?

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.

efficacy of combining Avonex and Copaxone; and a natural history study, as an adjunct to the Avonex/Copaxone study. I declined all of them as I live about 450 kms from the research facility and being in a study involves monthly follow ups. Winter was around the corner, I was overwhelmed by my dx, and did not want to make a commitment to be doing all that travel. In hindsight I wish now that I had opted to do the Avonex/Copaxone study.

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