Mr. Ibrahem/Bromfenac
Clinical data
Trade namesBromday, Xibrom, Prolensa, Yellox, others
AHFS/Drugs.comMonograph
MedlinePlusa611018
License data
Routes of
administration
Eye drops
Drug classNSAID[1]
Legal status
Legal status
Pharmacokinetic data
Protein binding99.8%
MetabolismCYP2C9
MetabolitesLactam, others
Elimination half-life1.4 hours in aqueous humour
Excretion82% urine, 13% faeces
Identifiers
  • 2-[2-amino-3-(4-bromobenzoyl)phenyl]acetic acid
Chemical and physical data
FormulaC15H12BrNO3
Molar mass334.169 g·mol−1
3D model (JSmol)
Melting point284 to 286 °C (543 to 547 °F) (bromfenac sodium·1.5H2O)
  • O=C(c1ccc(Br)cc1)c2cccc(c2N)CC(=O)O
  • InChI=1S/C15H12BrNO3/c16-11-6-4-9(5-7-11)15(20)12-3-1-2-10(14(12)17)8-13(18)19/h1-7H,8,17H2,(H,18,19) checkY
  • Key:ZBPLOVFIXSTCRZ-UHFFFAOYSA-N checkY
  (verify)

Bromfenac is a nonsteroidal anti-inflammatory drug (NSAID) which is used for pain and inflammation after cataract surgery.[1] It is used as an eye drop twice per day for two weeks.[1]

Common side effects include red eyes, itchy eyes, and headache.[1] Other side effects may include slower wound healing, bleeding, and keratitis.[1] It works by blocking the production of prostaglandins.[1]

Bromfenac was approved for medical use in the United States in 2005.[1] It is available as a generic medication.[2] In the United States 1.7 ml of 0.09% solution costs about 51 USD as of 2021.[2] In the United Kingdom 5 ml of the solution costs the NHS 8.5 pounds.[3]

References edit

  1. ^ a b c d e f g h i "Bromfenac Monograph for Professionals". Drugs.com. Archived from the original on 21 January 2021. Retrieved 17 July 2021.
  2. ^ a b "Bromfenac Prices, Coupons & Savings Tips - GoodRx". GoodRx. Archived from the original on 26 May 2020. Retrieved 17 July 2021.
  3. ^ BNF (80 ed.). BMJ Group and the Pharmaceutical Press. September 2020 – March 2021. p. 1241. ISBN 978-0-85711-369-6.{{cite book}}: CS1 maint: date format (link)