Rebif users

Common Questions and Answers about Rebif users

rebif

Avatar f tn //www.medhelp.org/posts/Multiple-Sclerosis/DMD-Users-Past--Present---Copaxone--Rebif--Avonex--Betaseron--Tysabri--other/show/1193746 Hope to help - please ask anything!
Avatar f tn I did some research on a more in-depth medical aspect and find no bad interaction with Rebif and Aspirin. In fact the swedish.org clearing shows in its rebif instructions that one can take up to 650mg of aspirin every 6 hours for relief from flu like symptoms. Perhaps you just got a weird reaction this time. I sometimes get a bad one from my Tysabri, for example, my last one was accompanied by a headache that lasted almost 24 hrs and then went away. But all others had been ok.
Avatar f tn A little frustrated and was wondering if any of you fellow rebif users have found things that have helped decrease your skin site reactions.
198419 tn?1360242356 //www.medhelp.org/posts/Multiple-Sclerosis/DMD-Users-Past--Present---Copaxone--Rebif--Avonex--Betaseron--Tysabri--other/show/1193746 The search feature is a beautiful thing - If you do not want to copy the links individually, just type "past and present" in the search feature - it will bring them all up for you.
439253 tn?1240835565 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.
1827617 tn?1317703371 My new neuro suggested Tysabri based on increased lesions on Interferon (Rebif). Any persons out there on Tysabri that could share their experience?
Avatar f tn Hi, His doc suggested Rebif or gilenya,. We are a little afriad of the gilenya because it is so new. You have to see so many specialist before you go on it. Do you know anyone on gilenya. Thanks for your input.
929431 tn?1247394932 org/posts/Multiple-Sclerosis/DMD-Users-Past--Present---Copaxone--Rebif--Avonex--Betaseron--Tysabri--other/show/1193746 -Shell
1710955 tn?1309446473 For all of you past and present Rebif users. Once you were on the 44mcg, did anyone notice a vast change in their mental well being? My anxiety is out of control. I am on meds for it and it does help, but it doesn't stop the attacks. My moods are all over the place, and I really think it's the Rebif. My docs know about this. My neuro wants me to continue the 44mcg, and I see him on the 19th.
Avatar m tn //www.medhelp.org/posts/Multiple-Sclerosis/DMD-Users-Past--Present---Copaxone--Rebif--Avonex--Betaseron--Tysabri--other/show/1193746 http://www.medhelp.org/posts/Multiple-Sclerosis/DMD/show/1041491 http://www.medhelp.org/posts/Multiple-Sclerosis/DMDs-experiences-please/show/759170 http://www.medhelp.org/posts/Multiple-Sclerosis/For-those-of-you-on-one-of-the-disease-modifying-drugs/show/471258 You may fair well with side affects.
1710955 tn?1309446473 Hi, Laura. I've been on Rebif, 4 and 1/2 months. I started on Copaxone, but after 6 and 1/2 weeks, we found out that my "side effects", were actually a severe allergy to it, The Rebif auto-ject is easy to use, and has the finest needle. I don't even feel it go in. And that is saying something, because I am 5'2 and weigh 77#s. I take an Advil for Migraines 1/2 hour before I inject. (I didn't get them until I was on it for just over 3 months.
497015 tn?1209737845 //www.medhelp.
Avatar f tn But anyhoo she gave me two medicine to read on betaseron and rebif. Both are injections I was told they have a new pill out that is very expensive and medcaid isn't paying at this time. I'm very uneasy abt the injections. Can anyone tell me if they've taken either one and their experience with it. I want another child in a few yrs and don't want this to stop me.
7463086 tn?1391008763 It is the lone injectable that is not an interferon and so acts differently to modify the disease. (Avonex, Rebif, Betaseron = interferons. Copaxone is Glatiramer Acetate.) I'll be honest, another reason I gave it a miss was the possibility of welts and lipoatrophy. What can I say? I'm vain! However I do think the latter is significantly lessened with vigilant injection site rotation.
3079363 tn?1363273715 Sorry HVAC! Delay of cancer drugs could be much more detrimental than waiting for MS drugs.I posted on Bubbles_04 post titled "Rebif Rant". The delay in getting the specialty drugs seems like a reoccurring problem.