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Hi I noticed a lot of comments on the "New" formulation of the Armour Thyroid tablets. I never got pills from my pharmacy with the "A" I swear all of mine were blank with no logo. I noticed this last batch has the "A" logo, is whiter and does not split in half well at all. Were there Armour tablets with no logo before? I am so confused and upset by this whole problem with this medication. I feel like buying a pig farm and learning how to make the stuff myself.
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!
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.
I have been on Rebif for four months now, and I am not going to do another shot, I can't handle the side effects. I've tried premedicating and nothing seems to work. How many of you are in the same situation? and what did you do?
I took my first shot of Rebif today. I gave myself the shot and i thought this is great no stinging, no redness, no lump like i had with Copaxone.
Then WHAM!!!! I had abdominal pain about an hour after the shot it lasted for about 6hrs
The only thing i could compare it to was a 6hr nonstop labor pain.
We will see what happens Monday when i take the next shot.
Does anyone else get this abdominal pain on Rebif.
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.
When I went to get my rebif refilled last week was tokd they were out and its on border and they don't kniw when it will come in and could be a couple months. I called every pharmacy in town and got.same.story. Then called rebif and they know.if.no shortage. Is anyone else.having this problem? In meantime I am out so no shots.
I've been on Rebif for about 13 years. My insurance recently stopped covering it, but offered Aubagio as an alternative--sounded good to me! I'll be switching, but I'm worried about just stopping Rebif cold turkey (which my neurologist suggests).
Has anyone had any experiences with stopping Rebif?
They were high, so at that point my neuro instructed me to go off all meds and supplements, and no alcohol, stayed on Rebif and they remained high when test was repeated. Went off Rebif, stayed off other meds and alcohol, they returned to normal, and remained so after I started other meds again and consumed alcohol again. This is how we could be certain it was Rebif causing the prolem.
Thanks for the suggestion. What are your favorite colors?
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