Grepafloxacin

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Grepafloxacin
Systematic (IUPAC) name
(RS)-1-cyclopropyl-6-fluoro-5-methyl-7-(3-methylpiperazin-1-yl)- 4-oxo-quinoline- 3-carboxylic acid
Clinical data
AHFS/Drugs.com Multum Consumer Information
Legal status ?
Pharmacokinetic data
Protein binding 50%
Identifiers
CAS number 119914-60-2 YesY
ATC code J01MA11
PubChem CID 72474
DrugBank DB00365
ChemSpider 65391 YesY
UNII L1M1U2HC31 YesY
KEGG C11368 YesY
ChEMBL CHEMBL583 YesY
Chemical data
Formula C19H22FN3O3 
Mol. mass 359.395 g/mol
 YesY (what is this?)  (verify)

Grepafloxacin hydrochloride (trade name Raxar, Glaxo Wellcome) was an oral broad-spectrum fluoroquinolone antibacterial agent used to treat bacterial infections. Grepafloxacin was withdrawn world wide from markets owing to its side effect of lengthening the QT interval on the electrocardiogram, leading to cardiac events and sudden death.[1]

GlaxoSmithKline marketed Raxar at doses of 200 milligrams, 400 milligrams and 600 milligrams. Records filed with the U.S. Food and Drug Administration (FDA) showed that Raxar was cited as a suspect in the reported deaths of 13 patients.[citation needed] There were four deaths associated with patients who took Raxar in 600-milligram doses within the clinical trials submitted with the New Drug Application (NDA) in 1997.[citation needed] The package insert approved by the FDA stated that "there were no deaths or permanent disabilities" among those who took Raxar in 400-milligram doses. It was the FDA’s position that none of the noted fatalities "was shown to be attributable to Raxar." On Oct. 27, 1999, GlaxoSmithKline removed Raxar from clinical use citing to the fact that Raxar's effect on "QT interval prolongation" was unacceptably risky. [2]

Other drugs within this class (i.e. sparfloxacin, moxifloxacin, levofloxacin, gatifloxacin, gemifloxacin) have also been associated with QT interval prolongation, resulting in sudden death of the patient.[3][medical citation needed]

See also

References

  1. Sprandel, KA.; Rodvold, KA. (2003). "Safety and tolerability of fluoroquinolones.". Clin Cornerstone. Suppl 3: S29–36. PMID 14992418. 
  2. http://www.mail-archive.com/sustainablelorgbiofuel@sustainablelists.org/msg54680.html
  3. Fluoroquinolones and QT prolongation research continues Prolongation of the QT interval is associated with potentially life-threatening ventricular tachyarrhythmias such as torsades de pointes. by Kimberly Madewell, PharmD http://www.infectiousdiseasenews.com/article/33493.aspx
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