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copaxone and severe chills

MS friends:  Had to stop copaxone, 30min after shot I would develop severe chills, with a neck ache and teeth chattering.  Would have to get in the shower for an hour, and still shivering, get into sweats and under 2 down comforters.  An hour later, it was over but I was physically wasted.  Has anyone else had such an experience?  Had to stop plegridy due to an allergic reaction.  What is out there that won't make me prone to infection, high blood pressure and liver damage?  Stats not so great on most of the drugs with preventing relapses or slowing them down for more than 40% than those taking a placebo.  Should I do nothing instead?  Thoughts?  Thanks .  Diagnosed Jan. 2015
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