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03-27-2018, 12:43 PM | #1 | ||
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The longer I live the more I see so much damage from drug interactions. Thank goodness I've worked with 95% supplements and avoid so many of the drugs. Had damage done in the past.
I posted a link on MrsD's posts about this class of drugs and it says DO NOT use for ITU's sinus infections, bronchitis....and yet it continues. |
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06-12-2018, 10:01 PM | #2 | |||
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I took Cipro many years ago when i early in my neuropathy travels. My get you were infected wire cellulitis and Cipro was the vascular guys choice. Within one
Day I felt lobotomized. I had no desire to get off my bed. I just sat on the side, neither drawn to get into, or out. My head seemed empty of thoughts, and I appreciated the paucity of thoughts. I always told doctors I was allergic, bit only after being diagnosed Lyme, did I learn that this was actually a rather topical jarisch herxheimer reaction. As a rule,I would thing these are too risky for us. Liza Jane reopening perhaps.
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LizaJane . --- LYME neuropathy diagnosed in 2009; considered "idiopathic" neuropathy 1996 - 2009 ---s/p laminectomy and fusion L3/4/5 Feb 2006 for a synovial spinal cyst |
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06-13-2018, 10:54 PM | #3 | |||
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From this article:
Quote:
Very telling, it so happens my sudden onset of PN was in 2011. Will research my medical history to see if I received a fluoroquinolone type drug.
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3/1/2011- diagnosed with Peripheral Neuropathy April 2012- Treated for Hepatitis C, achieved SVR |
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06-15-2018, 07:20 AM | #4 | ||
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I don't think I have ever taken any Fluoroquinolones, or if I did it was only for a short period. So at least for me I don't think they are related to my PN.
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