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ketorolac

ketorolac

introduction:

  • Structurally & pharmacologically related to tolmetin & indomethacin, however, unlike these pyrolle acetic acid derivatives, it is a cyclic propionic derivative.
  • It is the most potent analgesic of the NSAID's & can be used in adults instead of narcotics to avoid the associated dependence problems of the narcotics.
  • if unavailable, consider 40mg parecoxib IM as an alternative parenteral NSAID analgesic

post-op. analgesia:

  • 30mg IM has onset of action & peak analgesic efficacy comparable to 12mg IM morphine or 100mg IM pethidine but has a longer duration of action.
  • 10mg IM is as efficacious as 6mg IM morphine
  • doses above 10mg IM or IV do not appear to have additional analgesic benefit but may increase risks1)
  • 10mg orally is superior to:

P/K:

  • Rapidly absorbed orally, peak [ ] @ 30min, T1/2 4-6hrs;
  • 99% plasma protein bound; Linear P/K after single dose;
  • Steady state after 6hrly doses for 1 day;
  • Mainly excreted in urine; poorly crosses BBB;

indications:

  • IM: Short term analgesia Rx (up to 2days) post-op
  • Oral: Short term analgesia Rx (up to 7days) post-op

C/I:

  • Obstetric use as PG inhib. effects on uterine contraction & fetal circulation;
  • Dehydration or hypovolaemia
  • Renal impairment (CRN > 180umol/L)
  • Coagulopathy
  • Post-op for ops. with high risk of bleeding
  • HS to NSAIDs
  • Pts with PH nasal polyps, angiooedema or bronchospasm/asthma
  • PH Stevens-Johnson synd. or vesicular bullous rash
  • Suspected or confirmed intracranial bleeding
  • GIT bleeding / PH peptic ulcer
  • Concurrent other NSAIDs
  • Pregnancy, labour, lactation, children < 16yrs.
ketorolac.txt · Last modified: 2025/05/31 03:42 by wh

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