Mr. Ibrahem/Gatifloxacin
Clinical data
Trade namesGatiflo, Tequin, Zymar, others
AHFS/Drugs.comMonograph
MedlinePlusa605012
Routes of
administration
Eye drops, by mouth (discontinued), IV (discontinued)[1]
Drug classFluoroquinolone[2]
Legal status
Legal status
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Protein binding20%
Elimination half-life7 to 14 hours
Identifiers
  • 1-Cyclopropyl-6-fluoro-8-methoxy-7-(3-methylpiperazin-1-yl)-4-oxo-quinoline-3-carboxylic acid
Chemical and physical data
FormulaC19H22FN3O4
Molar mass375.400 g·mol−1
3D model (JSmol)
  • Fc1c(c(OC)c2c(c1)C(=O)C(\C(=O)O)=C/N2C3CC3)N4CC(NCC4)C
  • InChI=1S/C19H22FN3O4/c1-10-8-22(6-5-21-10)16-14(20)7-12-15(18(16)27-2)23(11-3-4-11)9-13(17(12)24)19(25)26/h7,9-11,21H,3-6,8H2,1-2H3,(H,25,26) checkY
  • Key:XUBOMFCQGDBHNK-UHFFFAOYSA-N checkY
  (verify)

Gatifloxacin, sold under the brand name Tequin among others, is an antibiotic used to treat bacterial conjunctivitis.[2] It is used as an eye drop.[2]

Common side effect effects include eye pain, abnormal taste, and increased redness of the eyes.[2] Other side effects may include allergic reactions.[2] It is in the fluoroquinolone family and works by inhibits the bacterial enzymes DNA gyrase and topoisomerase IV.[2]

Gatifloxacin was patented in 1986 and approved for medical use in 1999.[3] The by mouth and injectable formulations were withdrawn in the United States in 2006 due to the side effects of high or low blood sugar.[1]

References edit

  1. ^ a b "Determination That TEQUIN (Gatifloxacin) Was Withdrawn From Sale for Reasons of Safety or Effectiveness". Archived from the original on 10 May 2021. Retrieved 3 December 2021.
  2. ^ a b c d e f g h "Gatifloxacin (EENT) Monograph for Professionals". Drugs.com. Archived from the original on 25 November 2020. Retrieved 3 December 2021.
  3. ^ Fischer, Jnos; Ganellin, C. Robin (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 501. ISBN 9783527607495. Archived from the original on 2021-10-31. Retrieved 2021-04-01.