Rebif fever
Common Questions and Answers about Rebif fever
rebif
http://www.mslifelines.com/rebif/guide/side-effects.
Hello, I have to try Rebif before my insurance will consider me for an oral DMD (since I've already been on Copaxone). I don't know too much about Rebif. I do know that it's an interferon and can cause flu like symptoms and I think it's intramuscular injections.
Do the injections hurt? Do you do the injections or does a nurse come out and give the injections? Are the injections in your legs? How often do you have to get the injections?
Rebif can cause flu-like symptoms - are you currently running a fever? How long have you felt sick?
Of course, it's very important to talk to your regular doctor about any symptoms. It may not be the Rebif that's causing your vomiting and shortness of breath.
A month or so ago, I had serious pain in my right leg. I thought it was an escalation of my spasticity - turned out it was a blood clot! I waited three weeks before seeking treatment.
Is anyone currently taking Rebif? And does anyone know anything about it? I was just (finally) diagnosed with MS, though my Neuro wouln't say which kind it was... and is planning on putting me on Rebif. It's been 2 years since my symptoms started, and haven't had any kind of relapse or relief in any symptoms, they just keep coming.
Hi Coach,
I'm on Rebif - and the dosing mgs is comparible to the Betaseron. It's the strongest in terms of interferons go - I do well with it and don't think you are at a disadvantage either way you go. Beta is th original and has the longest track record.
For what it's worth, I do well with it. Super slim needle and only 3 x's a week injection.
Others should come along and send their experiences as well.
That is the best outcome. Rebif, nor any of the other three firstline meds, are considered cures. Rebif is an excellent med with a good reputation. And therer are other meds that are coming along soon that will be in pill form, but it remains to be seen who will do best on those versus using the shots.
Now, the reality is that a good proportion of people with MS will need some aid for walking and other activities (like a cane or wheelchair) within about 20 to 25 years after diagnosis.
Well, I've been on the Rebif just over 3 months and I am suffering with hot & cold flashes.
Do these go away?
I'm not getting enough sleep at night.
And my eyes have become extremely sensitive to light. But I don't know if that is connected to Rebif or just the MS.
Anyone else?
Optic nuritis 2 times loss of facial movement all kinds of things. I have been on Avonex and now rebif. I recently stopped taking rebif it was making me have a fever and just feel crummy. It's been 5 week s and I feel great.I'm concerned with not taking it I may have a large relapse. Iv changed my diet all natural food any thoughts on this?? Was thinking of starting it again but just don't want that feeling.
I have MS and have been taking Rebif foe 7 years. It has worked very well. I just learned that my current drug insurance plan from Humana will not cover Rebif in 2015. What plans cover at least some of the Rebif cost? My copay with Humana was about $300 per month. Would like not to exceed this amount.
So the ins company wont pay for Copaxone or Gilynia until my daughter first tries Rebif (i guess because its cheaper for them.) I have a concern with her being on an interferon due to the possible mental health side effects. She is already on Lexapro for anxiety and mild depression. I dont want anything adding to the issue. We have dr app tomorrow to discuss Rebif but I dont want her on it. Anyone have bad side effects with Rebif??? Any advise for me?? Thank you.
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