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FDA, researchers looking into prescription drug after complaints (Cipro/Fluorouquinolones)

JPV

ɹǝqɯǝɯ ɹoıuǝs
Messages
858
FDA, researchers looking into prescription drug after complaints

(WRIC) — 8News has confirmed complaints about some commonly prescribed antibiotics are now getting new attention from the FDA and medical researchers.

Cipro, part of a family of drugs called Fluorouquinolones, is powerful enough to treat anthrax and is widely prescribed for everything from ear infections to sinus infections.

We’ve confirmed that the FDA recently met with a group of folks who believe these popular antibiotics were nothing but a prescription for pain.
 
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dannybex

Senior Member
Messages
3,564
Location
Seattle
A lot of people have known for years that cipro is really bad. I can't believe it's taken them this long.

I told my doctor that I'm allergic to that class of abx.

Yes, Cipro has had a black box warning on it since 2008 regarding tendon rupture, but the point of this story was that stronger warnings are warranted as the FDA also has known since at least 2013 that these ABX also damage the mitochondria.
 

slysaint

Senior Member
Messages
2,125
Just received this update from Lisa Bloomquist:

Huge Gains in Fluoroquinolone Toxicity Awareness
In July, 2016, the FDA announced that major changes are to be made to the warning labels for all oral and IV fluoroquinolone antibiotics - Cipro/ciprofloxacin, Levaquin/levofloxacin, Avelox/moxifloxacin, and a few others. Not only is the FDA acknowledging the devastating effects of fluoroquinolones, they are warning people, in the highlighted black-box warning section, that fluoroquinolones are connected with, "disabling and potentially irreversible serious adverse reactions that have occurred together." This acknowledgement from the FDA is a HUGE step in the right direction.

The updated black-box warning for Cipro/ciprofloxacin states:

WARNING: SERIOUS ADVERSE REACTIONS INCLUDING TENDINITIS, TENDON RUPTURE, PERIPHERAL NEUROPATHY, CENTRAL NERVOUS SYSTEM EFFECTS AND EXACERBATION OF MYASTHENIA GRAVIS

  • Fluoroquinolones, including CIPRO®, have been associated with disabling and potentially irreversible serious adverse reactions that have occurred together including:
    • Tendinitis and tendon rupture
    • Peripheral neuropathy
    • Central nervous system effects
  • Discontinue CIPRO immediately and avoid the use of fluoroquinolones, including CIPRO, in patients who experience any of these serious adverse reactions. Fluoroquinolones, including CIPRO, may exacerbate muscle weakness in patients with myasthenia gravis. Avoid CIPRO in patients with known history of myasthenia gravis.
  • Because fluoroquinolones, including CIPRO, have been associated with serious adverse reactions, reserve CIPRO for use in patients who have no alternative treatment options for the following indications:
    • Acute exacerbation of chronic bronchitis
    • Acute uncomplicated cystitis
    • Acute sinusitis
The other updates to the Cipro/ciprofloxacin warning label can be viewed HERE.
The other updates to the Levaquin/levofloxacin warning label can be viewed HERE.
The other updates to the Avelox/moxifloxacin warning label can be viewed HERE.
 

Gingergrrl

Senior Member
Messages
16,171
Not only is the FDA acknowledging the devastating effects of fluoroquinolones, they are warning people, in the highlighted black-box warning section, that fluoroquinolones are connected with, "disabling and potentially irreversible serious adverse reactions that have occurred together." This acknowledgement from the FDA is a HUGE step in the right direction.

ITA it is a step in the right direction but most doctors will not pay any attention to this and will continue to prescribe Cipro & Levaquin to patients as if it were candy and not give them any warnings :mad::aghhh::nervous::bang-head:.