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The following post marketing reports are from the Quinolone Adverse
Drug Reaction Forum hosted by Yahoo, which is independently owned and
operated and has no association with the Fluoroquinolone Toxicity
Research Foundation.
This personal story was
originally posted to the Quinolone Adverse Reaction Forum. If you are
a victim of a quinolone antibiotic and need support or advice then
please visit the Quinolone Adverse Reaction Forum (http://groups.yahoo.com/group/quinolones/).
Post Marketing Reports from Drugvictims.org
Cipro
Posted on 28 October 2002
Hi all, I'm back after probably 6 months of not reading the forum at
all.
To recap, I'm a 29 year-old male. Next week will be my 1 year
anniversary since taking 6 doses of Cipro 500 mg. Overall, I have
improved a lot since the early days. My tendons and joints are better.
I can walk normally again. My brain is better. My muscle twitching is
better. My balance is better. My taste buds have returned to normal.
The nausea is gone. But things still linger for me.
I still have not attempted to run or long jump since Cipro. I am
hopeful to try this again sometime, but I'm still building up my
confidence. I have been getting back into swing dancing in the past
month without much problem. My achilles tendons usually hurt in the
morning when I wake up, but after an hour or two they feel ok.
My eyes still have a mild burning sensation most of the time. I cannot
focus as well at a distance. It seems that when I focus close up for a
while that my eyes cannot then focus at a distance. I never had this
problem before, but it seems to me that my lenses and/or muscles and
tendons in my eyes must be stiff like the rest of me.
I still have mild muscle twitching about once or twice a day. It can
happen just about anywhere on my body. My muscle tremors seem to have
subsided, and a lot of my strength has returned.
I still have various pains that act up in various places. It can
change daily, and seems to have no real rhyme or reason.
I still have Cipro moments sometimes, where I can't remember a word I
know I should be able to, or a name.
My craving for chicken and turkey has mostly subsided. I basically
don't eat them anymore.
About 5 months into my ADR, I suffered a collapse of my left lung.
Spontaneous pneumothorax for all the medical terminologists. This
culminated in surgery and two microstaples in my lung to patch it up.
Of course, the surgeons felt this was completely unrelated to my Cipro
injuries. A spontaneous lung collapse is usually due to tiny defects
in the lung that have been present since birth. And the surgery
revealed that I had those defects. I agree that I was predisposed to
the collapse, but it seems reasonable that since the Cipro attacked
various connective tissue, it could have weakened those defects as
well.
Like probably anyone here, I have been thankful for the victories. The
first time I went out dancing again in about a year was really special
for me.
But now that I am mostly back on my feet and better able to deal with
normal life and my ADRs, and realizing that nobody really knows what
lies ahead for me, I've been wondering about the case for legal
action. I know that lawyers cannot restore my health. But what can be
done to change an entire healthcare system that seems to be spiralling
toward profits at the expense of patient wellbeing?
Hope everyone continues to improve, and that we continue to learn more
about our conditions. Take care, Rob
Originally posted on the Quinolone Adverse Reaction Forum at http://groups.yahoo.com/group/quinolones/message/10374
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