Originally posted by kinnarde
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Originally posted by Myoak View PostFor more about Teva slowing down Biogen getting FDA approval for BG-12 here is a link, if no one has posted it:
http://www.globes.co.il/serveen/glob...did=1000813353Diagnosis: May, 2008
Avonex, Copaxone, Tysabri starting 8/17/11
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it's all about money...
I lost a ton of respect for Teva, aside from their nurse saying that "depression is NOT a known side-effect of Copaxone". I forgave them for that, but this is inexcusable to me!!! Where's the goodwill, the caring for patients, the image that they are a partner in getting MS cured? Or, is it that ONLY Teva can be the maker of effective MS drugs...?
oh well
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BG-12: EMA CHMP Panel Result ?
I was on the FDA Calendar webpage and saw a decision will be made on March 28th.
When I scrolled further down I saw Now-06/30/13 an EMA CHMP Panel Result. Does this have anything to do with the FDA decision on the 28th of March?
Also can anyone clarify if the decisions the EU, EMA and FDA matter to one another?I left in love, in laughter, and in truth, and wherever truth, love and laughter abide, I am there in spirit.
Bill Hicks
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BG-12 ->Tecfidera Approved!
I was at my Neurologist as the bell closed on Wall Street yesterday 3.27.2013. We did a refresh, went to google and there we saw it! Tecfidera approved by FDA! I see my Neurologist in 3 weeks and will be ready to start BG-12!
I just want to thank everyone for writing to the FDA & CDC. All the different MS entities for their hard-work and all the fellow MSers who volunteered in the earliest of studies with BG-12. You are the heroes!
Thank you for all you have done.I left in love, in laughter, and in truth, and wherever truth, love and laughter abide, I am there in spirit.
Bill Hicks
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