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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
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/).
Levaquin
Posted on 28 March 2002
Hi, all …
I'm a newcomer to this forum, having become yet another
fluoroquinolone statistic. I'm posting my story here because I need to
do some major venting. Frankly, I hope to never lay eyes on another
pompous M.D., or facsimile thereof, again in my life … unless, of
course, my arms fall off or something. In any case, this tirade is
probably going to make for a lengthy post, so my apologies in advance
…
I am a 31-year-old male and I was referred to my doctor's "good
urologist buddy" back in January for what was supposed to be some sort
of low-level prostatitis. The symptoms I was experiencing from this
were in no way debilitating and were, if anything, an annoyance. But
in a decision that I now regret, I decided to take my doctor up on his
referral. In late January, I paid a visit to this urologist who
confirmed the suspicions of my PCP, saying that, yes indeedy-do, he
was 95% certain that I had some "low-level prostatitis" going, so he
prescribed Levaquin.
The regiment seemed extensive: 500 milligrams a day for 42 days.
Having never had problems with antibiotics (or ANY prescribed
medication, for that matter) before, I threw away the insert without
even reading it, thinking that I had every reason to do exactly as the
good doctor ordered: one capsule per day for 42 days—"the full dose
every time." (Anybody ever seen "Wit"?)
After about the 10th day or so, I noticed my right eye twitching. This
lasted about a week and I didn't associate it with the Levaquin. After
about the 20th day, I started noticing some even stranger goings-on. I
had begun an exercise and yoga regime just after Christmas, and by
mid-February, I noticed that it was becoming more difficult to hold
some of the yoga poses—my body would shake under the strain and my
balance was worse than ever. I was also becoming tired a lot and when
I tried to close my eyes to take naps, it would feel as if the room
was spinning, similar to that feeling you get right after being shaken
very, very hard. The thought still never crossed my mind that it could
be the Levaquin—I mean, it was just some little harmless antibiotic,
right?
So, I continued to brush off these oddities until later in
February—after almost 30 days of taking the Levaquin. I was driving
back to work from my lunch break when suddenly my right thumb started
to twitch like it had a mind of its own. By the time I got to work,
the quivering was running all the way up my right arm into the side of
my head; I felt like I had palsy or something. Still not associating
it with the Levaquin, I immediately turned to the internet in an
impulsive and frantic attempt to figure out what was wrong with me.
Well, this was Mistake #2. Instead of assuaging any anxiety, my search
just made things worse: MS! ALS! MYASTHENIA GRAVIS! FIBROMYALGIA!
BRAIN TUMOR! All sorts of fun NEUROPATHY! But the horror story I
really became obsessed with was PARKINSON'S DISEASE! Yes, I really
believed I had Parkinson's, and this led to a really fun two-day
series of—you guessed it—PANIC ATTACKS.
That's right, for two days I lived in a nightmare. I was convinced I
was going to die, and I thought I was going crazy to boot: pacing
restlessly, shaking, quivering, feeling like I was going to jump out
of my skin. I finally gave in and told a friend what was going on, and
that helped a lot. Through all that haze, somehow I began to think a
little more rationally. What I was feeling was completely out of the
ordinary, almost chemical, like a drug trip or something. Could it be
the antibiotic? The Levaquin? Still not entirely convinced that a
simple antibiotic could cause such bizarre symptoms, I nevertheless
returned to the internet for a search on this drug.
What I read was both a relief and yet another source for
disturbance—to find that so many others were having similar,
unrelenting reactions to this God-forsaken drug and that it is STILL
being prescribed to unsuspecting saps like me was disconcerting. I
stopped taking it immediately, and a couple weeks later I went back to
the urologist for my six-week follow-up.
And it was after my second visit to the urologist that I decided I
loathed the medical profession. After sitting in the waiting room for
almost an hour with nothing to do but read a six-month-old copy of
"People" and the "Good News" bible, after getting highly p.o.'d at the
receptionist who not only yelled my name across the waiting room but
asked personal questions in full earshot of the other waiting
patients, after finally making it in and telling the urologist about
what this medicine had done to me, what does he do? He cuts me off and
holds up his finger and says, "One percent. Just one percentof
patients have side effects from this drug and it's usually the
elderly. I wouldn't have prescribed it if I thought it would do that."
I didn't even argue with him. I could see that he was just protecting
himself and trying to make me think I was just a hypochondriac. I did
tell him I was going homeopathic all the way from now on, to which he
replied snidely, "Well maybe you can educate me on that." Truth be
told, I'm sure he really does believeme, but he had to protect
himself. The era of people helping people is gone. Doctors have been
reduced to soulless androids.
So where am I now, a month after taking my last dose of Levaquin? I'm
somewhat better, but it comes and goes. I still have a lot of problems
with twitching and shaking all over. I don't have as much anxiety as
before and the panic attacks are gone, but I still tire very easily
which isn't much of a motivator to engage in all the activities I once
enjoyed. In any case, I'm glad this group is here (although I bewail
the fact that it's necessary), and I feel better having posted this
story. Thanks to all who listened! Mark
Originally posted on the Quinolone Adverse Reaction Forum at http://groups.yahoo.com/group/quinolones/message/7252
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