FDA Proposal Should Anger FQ Community
The fox is constantly trying to get into our hen house to control the data we read, control our narrative, and control our perceptions and the FDA is allowing this to happen.
The fox is constantly trying to get into our hen house to control the data we read, control our narrative, and control our perceptions and the FDA is allowing this to happen.
This website was created by a fellow floxie and friend to describe how Fluoroquinolone Toxicity (FQT) permanently damaged their Thyroid Hormone and Iodine metabolism (TH/Iodine metabolism).
The FDA has also failed to act on the Citizen’s petition for FQ Psychiatric adverse events submitted by Dr. Bennett and SONAR submitted in September of 2014.
Although this mutation is fairly uncommon, however if you do have this mutation it can significantly impact many areas of your health.
Do we welcome an organization into our midst that; employs former pharmaceutical execs? Sponsors events attended by pharmaceutical companies? Most of which have connections to Fluoroquinolones?
David from My Quin Story and another FQ sufferer is interviewed by Erin Kennedy from CBS WBBM Chicago.
The media attention is now growing surrounding Fluoroquinolones. We must keep the momentum moving. The media is being told there are thousands suffering, which I know to be true, the time is right to: Tell Your Story: Be Heard
More than 3,000 people have died after taking one of these antibiotics and hundreds of thousands of people have been damaged by these antibiotics. We can wait no longer. These deaths and destroyed lives were preventable.
I have found that there is a great misconception by many, including doctors, about the concept of senescence. Most believe it is just simply ‘old age’, but its far more....
The FDA has been derelict in their duty to fully warn the general public of the dangers these drugs pose to the general public. Its time for everyone to write in and be heard.
This is the popular report from WSB-TV Atlanta, GA on averse reactions to Levaquin.
Recently an internal memo dated April 17, 2013, issued by the Food and Drug Administration’s Center Drug Evaluation and Research, Office of Surveillance and Epidemiology, was obtained through the freedom of information act shows the FQs in a damning light.
Steroid Usage, the subject is controversial in individuals who [...]
When researchers have the mindset that the current usable formulary of FQ’s is a goal to reach based on safety and efficacy then the premise of their research is flawed.
A simple three step action that logically links FQ’s to the ability to initiate delayed adverse "late effect" reactions. There are no grand leaps of faith or conjecture required to link the steps.