CERTAIN ADVERSE EVENTS
 This documentary puts a human face on the suffering
 of those who have suffered an adverse reaction to the
 fluoroquinolones.  As well as an in depth analysis of the FDA's
 failure to protect the patient.  How can a hand full of antibiotics
 destroy one's life?  This film attempts to answer that question.
 

  BLACK BOX WARNING ADDED   
 
The FDA notified makers of fluoroquinolone antimicrobial
  drugs for systemic use of the need to add a Boxed Warning
  to the prescribing information about the increased risk of
  developing tendonitis and tendon rupture in patients taking
  fluoroquinolones and to develop a Medication Guide.

 

  LITIGATION TENDON ISSUES
  
If you have suffered a tendon rupture or other tendon injury as a
  result of being on a fluoroquinolone drug there are a number of
  legal firms that are accepting such cases.  Currently there are
  a significant number of product liability cases pending in Federal
  Court involving levofloxacin/ofloxacin.

 
  SURVEY REQUEST 
  It is strongly recommended that you fill out a Med Watch Report as
  well as taking a moment to fill out our Patient Survey form (only 16
  questions).  Post Marketing Reports are very important in identifying
  unusual adverse reactions.  You need not use your name or e-mail
  address to assure your privacy in your response. 

 
  FQ Toxicity YAHOO DISCUSSION FORUM 
 
This is our original discussion forum hosted by Yahoo.  This forum
  has been made available to the victims of the horrendous adverse
  reactions associated with the fluoroquinolones as a courtesy of
  FQresearch.  All visitors are invited to join this forum.
  Yahoo Group Forums:http://groups.yahoo.com/group/fqtoxicity


 
  PATIENT STORIES
  
We are encouraging visitors to submit their own stories and
  describe how these drugs have affected their life. A number
  of victims describe in vivid detail how their lives had been
  destroyed due to the careless scripting and abuse found
  within this class.  Please join them in telling your story.

 
  FLUOROQUINOLONES IN CLINICAL PRACTICE
 
The fluoroquinolones are NOT to be considered a first line agent
  for any disease state.  They are to be considered a drug of last
  resort when all else fails.  Though a necessary tool to be found
  in the physicians arsenal, they are approved for very few if any
  minor infections.  We have compiled a list of approved usage
  as well as the proper clinical guidelines for visitors to review.
 
  WHAT IS AN ADVERSE REACTION? 
  An adverse drug reaction (abbreviated ADR) is a term to describe
  the unwanted, negative consequences associated with the  use of
  different medications. ADR is a particular type of adverse effect.  The
  term is preferred over the colloquial and imprecise "side effect", as
  the term "side effect" implies that the effects are not explained by
  the pharmacological actions of the drug.
 
  SYMPTOMS
   To look up a symptom by name just Click Here to see a list of
   adverse drug reactions to the fluoroquinolones beginning with that
   letter.  For general information regarding a condition we suggest that
   you log unto Google and do a search. There are any number of
   medical sites online that would be able to provide the basic
   background  regarding such conditions.
 
  THE FDA AND THE FLUOROQUINOLONES
  The Food and Drug Administration is responsible for assuring that all
  drugs are both safe and effective, carrying minimal risk to the patient.
  Of course some drugs are extremely toxic and dangerous and their
  use is restricted to such cases that the benefits outweigh the risk.
  But the FDA refused for more than fourteen years to add "Black Box"
  warnings to these drugs and continues to approve new drugs in this class.
 
  PUBLIC CITIZEN
  Dr. Sidney Wolfe, of Public Citizen, has filed numerous petitions with
  the FDA seeking proper warnings and in some cases the removal of
  the drug from clinical practice.  The FDA has all but ignored these
  petitions and has continued to allow the careless scripting of these
  drugs and has failed to provide for adequate warnings to the patient.
  Everything found on this site has been forwarded to the FDA.
 
  READ THE DRUG LABELS
 
The proper use of any prescription drug requires that the physician
  engage in a Risk / Benefit discussion with the patient. This must
  include all of the relevant risk information being made available to the
  patient as well as the potential benefit to be derived from taking the
  medicine.  Informed consent cannot be obtained absent of such a
  discussion.
 
  FLUOROQUINOLONE TRIVIA
 
It has been estimated that more than 10% of the world's population
  has been prescribed a fluoroquinolone.  Yearly sales are well into the
  billions of dollars.  Any number of these drugs have been removed
  from clinical practice due to severe adverse reactions including
  fatalities.  Many foreign governments, as well as the United Nations,
  have banned a large number of the fluoroquinolones.
 
  SCRIPTING ABUSE
 
Scripting abuse runs rampant and for the most part the
  treating physician has no idea how dangerous the fluoroquinolones
  truly are.  Even though these drugs are to be considered a drug of
  last resort when there is no other alternative available, they are
  handed out like Halloween candy for the most frivolous reasons. 
  Recently the FDA has approved clinical trials for pediatric use.
 
  POST MARKETING SURVEILLANCE
 
In theory the FDA's Med Watch program is supposed to alert the
  FDA to any adverse reactions that develop once the drug is in clinical
  use but in practice this program is useless.  Less than 4% of all
  such events are ever reported to the FDA.  On the Internet there are
  forums that discuss these events and the number of members is in
  the tens of thousands, yet the FDA has shown no  interest in this.
 
  IN THE NEWS
 
We have accumulated thousands of newspaper and magazine
  article that detail the horrendous damage caused by these drugs. 
  since the 1930's such events have been reported in the media,
  including deaths, yet the patient continues to be unaware of the risk
  associated with fluoroquinolone therapy.  The treating physician also
  continues to deny any such association.
 
  ADVOCACY
 
All that is required for such evil to continue is for the victims to
  remain silent.  We, who have had are lives destroyed by these drugs,
  have refused to do so.  We have petitioned the FDA, written letters to
  the media, members of Congress, as well as the medical and legal
  community since 1999.  We shall continue to be tenacious in our
  efforts to inform the public of the real safety profile of the Quinolones.
 
  CITATIONS AND DOCUMENTATION
 
Since the 1930's such events have been reported in the leading
  medical journals.  We have accumulated well over 4000 such journal
  entries, case reports, newspaper articles, etc., that support all of the
  claims being made within these web pages.  Since  the introduction
  of Chloroquine in 1934 serious adverse events have been associated
  with these synthetically manufactured drugs.
 
  DOCTORS, RESEARCHERS AND PHARMACISTS
  Most physicians have little to no training when it comes to
  adverse drug reactions.  You will find that most physicians will deny
  any association with these events and fluoroquinolone therapy.  The
  average researcher is employed by the drug companies and "ghost
  writes" articles that praise the fluoroquinolones while research into
  the side effects is ignored.  Pharmacists are rarely kept up to date.
 
  PROPAGANDA
 
The amount of false information and misleading statements
  regarding the safety profile of the fluoroquinolones is staggering.
  Numerous drug manufacturers have received warning letters from
  the FDA but that has not stopped the aggressive marketing of the
  drugs.  Fraud, unethical clinical trials, dissemination of misleading
  information have all been a contributing factor to this.
 
  ADOBE PDF FILES
  As a number of documents found on this site go back sixty to
  seventy years you will find them to be PDF files.  In order to access
  such files you have to have Adobe Reader loaded on your computer. 
  This utility is available from Adobe at no charge.  PDF files is one of
  the original  file formats used when the Internet first came into
  existence and  for years has been the format used.
 
  DONATIONS
 
This web site is being offered as a free public service.  We do not
  accept any donations, financial support or advertising of any kind. 
  Visitors are under no financial obligation what so ever as a result of using
  this web site.  However it takes a tremendous amount of time and effort
  to educate others and to in reach out to those who have suffered in
  the same fashion as you have.  So please share this site with others.

 

                          THE CORRUPTION NEVER CEASES
 
                         

       All that is required for the victims of adverse drug reactions to be frustrated in any attempt to
  sue the drug manufacturers is for the medical community to deny any such proven association.
  If it is not generally accepted in the medical community that these drugs can cause this type
  of damage, then the victims will forever be denied their day in court due to draconian Daubert and
  Frye Standard of Proof.

  "Drug companies write the package inserts of all drugs, carefully including the information
  they choose and omitting information they want to avoid. Drug companies underwrite a large
  percentage of continuing education courses for doctors. In doing so, they make sure that the
  speakers represent the company view. Drug companies design studies that are meant to
  produce favorable results and then publish the studies in medical journals. Studies with
  unfavorable results are not published. Drug reps typically bring stacks of studies, all
  favorable, which impress doctors, who no longer have the time or motivation to search the
  medical literature themselves. Drug reps do not include independent studies with less
  favorable conclusions. Many doctors never see these." 

  Source: 
 THE MEDICAL PROFESSION AND THE CULTURE OF CORRUPTION


                               

                 The Fluoroquinolone Toxicity Research Foundation
                                              
(Read More)

       The foundation is an Internet Community consisting of those who have suffered severe and
  permanent injuries due to fluoroquinolone therapy.  We acquire information from all over the
  world and present this information to both the patient and the physician.  It is our hope that
  one day that the treating physician will be in a position to entertain a rational and factual risk
  benefit discussion prior to prescribing these drugs.  The fluoroquinolones are a very important
  tool to be found within the physician's arsenal for treating serious and life threatening
  diseases.  However this is not the manner in which they are prescribed today. 

       The Foundation supports the numerous adverse reaction forums found on the Internet so
  that patients who have suffered such reactions will have a place to turn for accurate
  information and moral support.  For the most part these reactions are life long chronic disease
  states that defy treatment.  There is no known treatment protocol and the ignorance found
  within the medical community is rampant.  We wish to change this.  One patient and one
  physician at a time. We hope that you would find something of value within these Web Pages
  and request that you take the time to fill out the patient survey, which consist of 16 short
  questions, as well as file a Med Watch report with the FDA.

  We also invite visitors to join our discussion forum hosted by Yahoo by following this link:

                    http://health.groups.yahoo.com/group/fqtoxicity/


    Fill Out The Survey             Read the Survey Responses            File A Med Watch Report 


           Copyright 2009 Fluoroquinolone Toxicity Research Foundation.  All rights reserved.