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Action: Inhibits COX-1 and COX-2 enzymes, resulting in decreased prostaglandin synthesis;
reduces prostaglandin levels in aqueous humor.
Indication: Ketorolac is indicate to relieve moderately severe pain, usually pain that occurs after
an operation or other painful procedure
Drug Interaction: May decrease effects of antihypertensives (e.g amlodipine, lisinopril), diuretics
(e.g furosemide, HCTZ). Aspirin, NSAIDs, other salicylates may increase risk of GI side effects,
bleeding. May increase risk of bleeding with heparin, oral anticoagulants (e.g. Warfarin). May
increase concentration, risk of toxicity of lithium. May increase effect of apixaban, dabigatran,
edoxaban, rivaroxaban. Bile acid sequestrants (e.g.cholestyramine) may decrease
absorption/effect. May increase nephrotoxic effect of cyclosporine.
Excretion: Around 92% of a dose is excreted in urine as 60% as unchanged ketorolac and 40% as
metabolites.
Adverse Effect: Peptic ulcer, GI bleeding, gastritis, severe hepatic reaction (cholestasis, jaundice)
occur rarely. Nephrotoxicity (glomerular nephritis, interstitial nephritis, nephrotic syndrome)
may occur in patients with preexisting renal impairment. Acute hypersensitivity reaction (fever,
chills, joint pain) occurs rarely.
1. Baseline Assessment: Assess onset, type, location, duration of pain. Obtain baseline
renal/hepatic function tests.
2. Intervention/Evaluation: Monitor renal function, LFT, urinary output. Monitor daily
pattern of bowel activity, stool, consistency. Observe for occult blood loss. Assess for
therapeutic response: relief of pain, stiffness, swelling; increased joint mobility; reduced
joint tenderness; improved grip strength. Monitor for bleeding (may also occur with
opthalmic route due to systemic absorption).
3. Patient/Family Teaching: Avoid aspirin, alcohol. Report abdominal pain, bloody stools, or
vomiting blood. If GI upset occurs, take with food, milk.