I recently stopped copaxone after a year. I loved the shared solutions program and the drug itself was well tolerated without major side effects EXCEPT about six months after I started I had severe, crushing chest pain. This happened about once a month and always at night time after lying down. They lasted twenty minutes and it felt exactly like you’d imagine a heart attack would feel liekX. The last one was so severe i fell to the ground.
This is a side effect that is listed in the prescribing pamphlet but I am just curious if anyone else experienced it.
unforunately I have not improved after a year on the drug so we have to change; also, due to the chest pain I cannot stay on copaxone.
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I am on Copaxone and I have had that happen along with shortness of breath, Its quite terrifying. I noticed it only happens on certain sites, I think I may have more vessels in that area so it enters my bloodstream and I get those attacks. It last for about 15 minutes and I have to constantly remind myself that itll go away to calm myself down.
HealthTalk perusers have been posting request for me about my current IPIR (Immediate Post Injection Reaction) attack while on Copaxone, Do My Homework
and on my fundamental authority get ready for changing MS pharmaceuticals