Gatifloxacin: Difference between revisions

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'''Gatifloxacin''' is an [[antibiotic]] of the fourth-generation [[fluoroquinolone]] family, that like other members of that family, inhibits the [[bacteria]]l [[enzyme]]s [[DNA gyrase]] and [[topoisomerase IV]]. [[Bristol-Myers Squibb]] introduced Gatifloxacin in 1999 under the [[proprietary]] name '''Tequin'''® for the treatment of respiratory tract infections, having licensed the medication from [[Kyorin Pharmaceutical Company]] of Japan.  Allergan produces an eye-drop formulation called '''Zymar'''®.  Gatifloxacin is available as [[tablet]]s and in various [[aqueous solution]]s for [[intravenous therapy]].
'''Gatifloxacin''' is an [[antibiotic]] of the fourth-generation [[fluoroquinolone]] family, that like other members of that family, inhibits the [[bacteria]]l [[enzyme]]s [[DNA gyrase]] and [[topoisomerase IV]]. [[Bristol-Myers Squibb]] introduced Gatifloxacin in 1999 under the proprietary name '''Tequin'''® for the treatment of respiratory tract infections, having licensed the medication from Kyorin Pharmaceutical Company of Japan.  Allergan produces an eye-drop formulation called '''Zymar'''®.  Gatifloxacin is available as [[tablet]]s and in various [[aqueous solution]]s for [[intravenous therapy]].


==Side-effects and removal from the market==
==Side-effects and removal from the market==
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  | url = http://content.nejm.org/cgi/content/abstract/354/13/1352
  | url = http://content.nejm.org/cgi/content/abstract/354/13/1352
  | accessdate = 2006-05-01
  | accessdate = 2006-05-01
}} ''Note: publication date 30 March; available on-line 1 March''</ref> An [[editorial]] by
}} ''Note: publication date 30 March; available on-line 1 March''</ref> An editorial by
Dr. Jerry Gurwitz in the same issue called for the [[Food and Drug Administration]] (FDA) to consider giving Tequin® a black box warning.<ref>{{cite journal
Dr. Jerry Gurwitz in the same issue called for the [[Food and Drug Administration]] (FDA) to consider giving Tequin® a black box warning.<ref>{{cite journal
  | last = Gurwitz
  | last = Gurwitz

Revision as of 14:58, 19 June 2009

Gatifloxacin
Clinical data
ATC code
Pharmacokinetic data
Protein binding20%
Elimination half-life7 to 14 hours
Identifiers
CAS Number
PubChem CID
DrugBank
E number{{#property:P628}}
ECHA InfoCard{{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
FormulaC19H22FN3O4
Molar mass375.394 g/mol

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Please Take Over This Page and Apply to be Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [2] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.

Gatifloxacin is an antibiotic of the fourth-generation fluoroquinolone family, that like other members of that family, inhibits the bacterial enzymes DNA gyrase and topoisomerase IV. Bristol-Myers Squibb introduced Gatifloxacin in 1999 under the proprietary name Tequin® for the treatment of respiratory tract infections, having licensed the medication from Kyorin Pharmaceutical Company of Japan. Allergan produces an eye-drop formulation called Zymar®. Gatifloxacin is available as tablets and in various aqueous solutions for intravenous therapy.

Side-effects and removal from the market

A Canadian study published in the New England Journal of Medicine in March 2006 claims Tequin® can have "life threatening" side effects including serious diabetes.[1] An editorial by Dr. Jerry Gurwitz in the same issue called for the Food and Drug Administration (FDA) to consider giving Tequin® a black box warning.[2] This editorial followed distribution of a letter dated February 15 by Bristol-Myers Squibb to health care providers indicating action taken with the FDA to strengthen warnings for the medication.[3] Subsequently it was reported on May 1, 2006 that Bristol-Myers Squibb would stop manufacture of Tequin, end sales of the drug after existing stockpiles were exhausted, and return all rights to Kyorin.[4]

Gatifloxacin is now only available in the US as an opthalmic solution.

Notes

  1. Park-Wyllie, Laura Y. (2006). "Outpatient Gatifloxacin Therapy and Dysglycemia in Older Adults". The New England Journal of Medicine. 354 (13): 1352&ndash, 1361. PMID 16510739. Retrieved 2006-05-01. Unknown parameter |month= ignored (help); Unknown parameter |coauthors= ignored (help) Note: publication date 30 March; available on-line 1 March
  2. Gurwitz, Jerry H. (2006). "Serious Adverse Drug Effects — Seeing the Trees through the Forest". The New England Journal of Medicine. 354 (13): 1413&ndash, 1415. PMID 16510740. Retrieved 2006-05-01. Unknown parameter |month= ignored (help)
  3. Lewis-Hall, Freda (February 15, 2006). "Dear Healthcare Provider:" (PDF). Bristol-Myers Squibb. Retrieved May 1. Unknown parameter |accessyear= ignored (|access-date= suggested) (help); Check date values in: |accessdate= (help)
  4. Schmid, Randolph E. (May 1, 2006). "Drug Company Taking Tequin Off Market". Associated Press. Retrieved May 1, 2006.


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