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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 24 July 1999
Hello Everyone, Thank you for sharing your stories and thank God for
the internet where we can share stories. So many of the stories posted
to this board are similar to mine. I am fortunate that my symptoms are
decreasing with time.
My ordeal began the first of this year when I had a mild female
infection. I was given a one week course of Levaquin. I became sicker
and unable to think clearly, fatigue, and malaise. At that time I had
a sense of something "settling in my bones." (I could tell the doctor
thought I was a nut case when I told him that!) My doctor believed
these increasing symptoms were due to an increased infection though
they could not find any organism that would cause anything close to
the symptoms I was having. Their answer - more levaquin!! After
finishing my second round of Levaquin I got arthritis in almost every
joint in my body, a rash on my chest, more fatigue, foggy brain. At
that time I got worked up for Lupus, Lyme Disease, Rheumatoid
Arthritis, Connective Tissue Disorder, checked my hormones,
thyroid,etc. All are negative. About a week ago my symptoms increased
and I ended up in the Emergency Room with an elevated white blood
count of 22.2 (it's usually 6.0). The doctor said he did not know the
cause of my problems but gave me a choice of leaving with another rx
of Levaquin or tough it out ( and risk endocarditis or meningitis) and
not treat it and get another blood culture to find the offending
organism. (there is no offending organism) Thank God I opted to tough
it out because I have been suspicious of the Levaquin but have been
"reassured" that Levaquin was not the cause of joint pain, foggy
brain, rash,etc. I believe what started out as a simple nonspecified
infection was transformed to a drug induced illness that has not been
recognized by multiple doctors. Levaquin should NOT be prescribed as a
first option for an antibiotic especially when the SIDE EFFECTS ARE
NOT RECOGNIZED OR CONSIDERED. The Doctors have been working on the
belief that my symptoms were increasing due to an unknown illness. Due
to their ignorance of the side effects of Levaquin - which they should
have taken into CONSIDERATION THAT THIS COULD BE A DRUG REACTION. I'm
still figuring all of this out but I bet it will play out that
Levaquin caused the arthritis, rash, malaise, muscle weakness,
headache, muscle weakness. The thing that outrages me is that when I
continued to report the muscle weakness and arthritis, so much so that
I could not push a shopping cart around the store is that they looked
at me like I was a nut case. My body was telling me something was
seriously wrong but my mind was getting foggier by the day and I was
WORRIED that I would become so sick that I would not be able to figure
out what was going on and play an active role in my recovery. Tell
something like that to a doctor and they think you're an hysterical
whacko woman. I've been told that it not so subtle ways. It's been
about a month since I've stopped the Levaquin and am slowly feeling
better. I still have a little arthritis, tendonitits, and transient
foggy brain but I can get around ok and manage my work. There have
been periods in the recent past when I could not manage my usual
duties at home and work.
Before all of this began I was an extremely healthy and strong 40 year
old female. I just came across this quinolone page last night. My
question is now; Has anyone else had an elevated white blood cell
count that was unexplained? A few of you have written here about
"serum sickness." What do you mean?
There is no damn excuse for Dr's who write the prescription for
Quinolone not to be able to recognize or acknowledge the drugs side
effects. Yes, I know there are risks to every medication, but nothing
was told to me in written form or verbally of these particular risks.
Even when I have the symptoms of an adverse reaction no one recognizes
it and further exacerbates the problem by prescribing it to me again.
I feel fortunate things turned out as well as they did for me. A few
lawsuits would bring this problem to the attention of those in the
medical field. There is no excuse for what is happening to people who
have another choice of antibiotics. THE RISKS SHOULD BE EXPLAINED
BETTER. I think few prople would opt to take the risk if they were
fully informed.
Thanks for listening. Once I get all my facts straight I'll be
pounding the pavement to the couple of doctors who have been involved
in my care (and prescribed Levaquin) and make them aware of what I've
learned and insist they become aware of the side effects. I hope they
listen..... Karen
Originally posted on the Quinolone Adverse Reaction Forum at http://groups.yahoo.com/group/quinolones/message/408
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