NATIONAL
CALIFORNIA
VENTURA
mechanism
  • Reversibly inhibits cyclooxygenase-1 and 2 (COX-1 and 2) enzymes, which results in decreased formation of prostaglandin precursors (lipid hormones which have a wide range of effects throughout the body); has antipyretic, analgesic, and anti-inflammatory properties
indications
  • Management of acute pain
contraindications
  • History of asthma, urticaria, or allergic-type reaction to aspirin or other NSAIDs
  • Cerebrovascular bleeding or other bleeding disorders
  • Active gastric/duodenal/peptic ulcer, active GI bleeding
  • Inflammatory bowel disease
  • Uncontrolled heart failure
dosing

Adult:

Weight ≥50 kg and <65 years of age:
IV: 30 mg
IM: 60 mg

Weight <50 kg or ≥65 years of age:
IV: 15 mg
IM: 30 mg

Pediatric:

IV, IM: 0.5 mg/kg; maximum dose: 30 mg

administration
IM: Administer slowly and deeply into the muscle
IV: Administer IV bolus over a minimum of 15 seconds
onset

30 minutes

peak

2 to 3 hours

duration

4 to 6 hours

notes
  • Side effects: Nonsteroidal anti-inflammatory drugs (NSAIDs) cause an increased risk of serious cardiovascular thrombotic and gastrointestinal events.
dosage form
Injection Solution: 15 mg/mL (1 mL); 30 mg/mL (1 mL); 60 mg/2 mL (2 mL)
brand name
Toradol
adverse reactions
  • Cardiovascular
    • Increased risk of serious adverse cardiovascular events, including acute myocardial infarction (MI) and cerebrovascular accident
    • Hypertension
    • Heart failure
  • Gastrointestinal
    • GI inflammation
    • GI hemorrhage
    • GI ulcer
    • GI perforation
  • Hematologic
    • Prolonged bleeding time
    • Hemorrhage
    • Hemolytic anemia
    • Thrombocytopenia (low platelets)
  • Hypersensitivity reactions
    • Angioedema
    • Urticaria
    • Stevens-Johnson syndrome (rare serious disorder of the skin and mucous membranes)
  • Kidney
    • Acute kidney injury
structure
ketorolac.svg molecular structure