FRCA Notes


Acetic Acid Derivative NSAIDs


  • A phenylacetic acid derivative
  • Used to treat mild-moderate pain and/or reduce opioid use
  • Particularly beneficial for renal colic
  • Side-effects limit its use

Presentation and dose

  • Oral, rectal, topical and parenteral (IV/IM) formulations
  • Adult dose 150mg/day (in divided doses)
  • Paediatric dose of 1mg/kg TDS

Pharmacokinetics

  • Oral bioavailability only 50%
  • Distribution
    • Highly protein bound: 99%
    • Small volume of distribution: 0.15 L/kg
  • Metabolised via hepatic hydroxylation/conjugation to inactive metabolites
  • Elimination half life 1-2hrs
  • Excretion in urine (60%) and bile (40%)

Pharmacodynamics

  • Cardiovascular: increased risk of coronary events with chronic use (similar to COX-2 inhibitors)
  • Gastrointestinal: reduced gastric irritation compared to aspirin and indomethacin
  • Renal: may precipitate renal impairment
  • Pain on injection:
    • IM route painful and may cause muscle damage
    • IV route may cause local thrombosis
  • Drug interactions: increases the plasma concentration of digoxin and lithium

  • A potent analgesic and anti-pyretic although as limited anti-inflammatory action
  • PO or IV/IM routes available
  • Doses
    • Adult: max 60mg/day in divided doses
    • Paediatric (<16yrs): 0.5-1.0mg/kg (max 15mg) every 6hrs
  • Maximum treatment duration 2 days

  • 99% protein bound
  • Elimination half-life of 5hrs

  • Similar side-effect profile to all NSAIDs
  • Contraindicated in those receiving heparin