rebif dosing

Does anyone know if there are any statistics showing the effectiveness of Rebif if used only twice a week versus three times a week? My husband will be losing his job come the end of August, and along with that, our benefits. I figure if I start now going to only 2 times a week, between now and the end of August I can make my Rebif last for at least another month. I know this is not the best thing to do, but it appears to possibly be the only solution.

I initially chose Rebif due to the dosing schedule. After 8 weeks I had to discontinue as my liver enzymes were very elevated on it. They returned to normal when I went off the drug. I only ever got up to the half-dose (22mcg) and wasnt on it long enough for it to do me any good. This liver reaction is apparently not that common, maybe 3% of pts according to the Serono's literature, and doesn't bother the majority of patients who take Rebif.

Hello. I was on Copaxone for 2 years. While on it I experienced several flair ups, so it's time to try something else. We decided on Rebif. Can any Rebif users out there give me any input on your experiences or helpful hints. I'm pretty nervous about the side effects but I am going in with a positive attitude. Thanks for the help.

He is now having me switch from Rebif to Copaxone after only two months. The only side effect I had on Rebif was red spots at the injection site. Wondering if anyone else has had this happen, and what side effects, if any Copaxone has compared to Rebif therapy. Thanks in advance for any responses.

Hi, Shell. Thanks. I wondered the same thing, if I might be getting a virus or the flu. I felt pretty bad all day yesterday, and it wasn't a good day to feel bad. (If there every is one) but it was my BFF's birthday, and we met for lunch and shopping. I have a horrendous headache this morning, starting from the base of my neck.

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.

Hard to answer your question without more information. Why do you have only those four choices? Avonex (which I’ve used for 11 years) and others are notably absent from your list. Avonex, Rebif, and Betaseron have been around longest and have the strongest safety profiles. If your MS is more aggressive, then you may be more inclined to consider Gilenya, Tecfidera, Aubagio, or Tysabri. All of the DMDs are discussed from a neutral perspective at the link below: http://www.nationalmssociety.

Hi Jen, We've not met. I'm Shelly and I'm on Rebif. You'll be contacted to receive your Rebif script, and a nurse covering your area will contact you to find a time to come visit (will also make sure you received the meds - which you'll keep in the fridge). He or she will teach you and whoever else you want to learn the injection techniques. The nurse will also talk to you about your MS, the meds and possible side affects, etc.

I saw my neurologist and he said that becuase I had recently had an increase in dosage of rebif it could be making me feel unwell. My symptoms were painful spacticity and urinary difficult (which were all new to me) and I'd swear I was having a relpase. I felt sicker than ever before with MS.

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?

I was diagnosed with MS in 2007 and used rebif for 7 years. I was doing well until late 2012. I started having problems with spasticity in my legs. At first I was able to control with baclofen but it continued to get worse and I started having weakness also. My MRI showed that there were no changes in 3 years, my antibodies test to rebif was negative but I continued to feel worse. In March my dr started talking about tysabri. I was freaked out but desperate to feel better.

First is some good news for Avonex and Rebif users. It looks like Biogen-Idec is going to be seeking marketing approval for monthly dosing later this year. http://www.medpagetoday.com/Neurology/MultipleSclerosis/36993?utm_source=share&utm_medium=mobile&utm_campaign=medpage%2Biphone%20app Second is kind of a double edged sword. The FDA has approved over the counter sale of Oxytrol, a drug aimed at overactive bladder. They have approved it for sale to women bu not men.

Hi Corrie, We have alot of discussion on our forum regarding varied experiences with the DMDs. I always suggest looking at your lifestyle and seeing what is a good fit for you. For example, look at the scheduling of dosing (Rebif 3x's weekly, Avonex 1x weekly, betaseron 4x's weekly and copax, once daily). Also, there are three orals - I would have to look up the dosing, but believe them to all be daily. My experience is with Rebif. Very tolerable, with a super thin needle.

Lisa - where you been? Your 1st Doc give you the info a bit ago? Or, is my brain getting folks jumbled...lol My personal experience is w/Rebif. I don't have the experience to comparision between each, but can speak to Rebif. I had all the typical flu-like symptoms they speak about. After a few months they did lessen greatly. My liver enzymes remained good throughout, though some on the board have had to go off due to elevated levels.

s the ms, the fact that i was recently diagnosed with ms, the rebif or just a bad few days, but i am NOT alright. lost my balance and fell yesterday... caught myself with my bad hand (the hand with the most discomfort and least motor function) on the spikes of a wrought iron fence. i bruised something pretty badly under the knuckle of my middle finger. i'm sure you can all imagine how happy i am to have added injury to an already insulting problem.

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.

d not hollar at or scold you for your decisions my friend, just giving it to you straight like I know you would me. When you are ready, maybe we can talk rebif, and sub-q and smaller dosing and compromises.

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.

Yes, I am on rebif for 11 months and must take advil liquid gels To stave off headache fever that wakes me up!

Call your local pharmacist. We at MedHelp are not allowed to give out dosing instructions. Your pharmacist will be able to tell you exactly how to dose the medications. If your regular pharmacy is closed on Sunday, call any pharmacist availabe at your local grocery store or drug store such as Walgreens, CVS, or RiteAid.

Common Questions and Answers about Rebif dosing

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