What is the recommended dosage of Toradol (Ketorolac) for patients?

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Last updated: September 12, 2025View editorial policy

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Recommended Dosage of Toradol (Ketorolac)

The recommended dosage of Toradol (ketorolac) for adults is 10-30mg IV/IM for initial dosing, followed by oral dosing of 10mg every 4-6 hours as needed, not exceeding 40mg per day orally or 120mg per day total, with treatment duration limited to a maximum of 5 days. 1, 2

Dosage Guidelines by Route of Administration

Intravenous/Intramuscular Dosing

  • Standard adult dosing (age 17-64):

    • Initial dose: 30mg IV or 60mg IM
    • Subsequent doses: 15-30mg IV/IM every 6 hours
    • Maximum daily dose: 120mg 1
  • High-risk populations (age ≥65, renal impairment, or weight <50kg):

    • Initial dose: 15mg IV or 30mg IM
    • Subsequent doses: 15mg IV/IM every 6 hours
    • Maximum daily dose: 60mg 1, 2

Oral Dosing (Only as continuation therapy after IV/IM dosing)

  • Standard adult dosing (age 17-64):

    • Initial oral dose: 20mg once
    • Subsequent doses: 10mg every 4-6 hours as needed
    • Maximum daily oral dose: 40mg 2
  • High-risk populations (age ≥65, renal impairment, or weight <50kg):

    • Initial oral dose: 10mg once
    • Subsequent doses: 10mg every 4-6 hours as needed
    • Maximum daily oral dose: 40mg 2

Important Clinical Considerations

Duration of Treatment

  • Combined duration of IV/IM and oral ketorolac should not exceed 5 days 1, 2, 3
  • Prolonged use significantly increases risk of serious adverse events, particularly in elderly patients 4

Analgesic Ceiling Effect

  • Research shows no additional analgesic benefit from doses exceeding 10mg IV 5
  • Using the lowest effective dose (10mg IV) provides effective pain relief with potentially fewer adverse effects 5

Contraindications

Ketorolac is contraindicated in patients with:

  • History of or current risk of gastrointestinal bleeding
  • Risk of renal failure
  • Compromised hemostasis
  • Hypersensitivity to aspirin or other NSAIDs
  • Pregnancy
  • Cerebrovascular hemorrhage
  • Aspirin/NSAID-induced asthma 1

Monitoring Requirements

  • Baseline assessment recommended for:
    • Blood pressure
    • BUN and creatinine
    • Liver function tests
    • CBC and fecal occult blood 1
  • Discontinue immediately if:
    • Renal function tests double
    • Hypertension develops or worsens
    • Liver function studies increase beyond normal limits 1

Special Populations and Considerations

Perioperative Use

  • For short-term perioperative therapy: 0.5-1mg/kg IV (up to 30mg) for a single intraoperative dose, or 0.15-0.2mg/kg (max 10mg) every 6 hours 1
  • Effective for postoperative pain management with potential opioid-sparing effects of 25-50% 4, 6

Cancer Pain Management

  • Can be administered via continuous subcutaneous infusion for cancer-related pain
  • Particularly effective for bone metastasis-related pain 7
  • May be mixed with opioids in syringe drivers for improved pain control 7

Emergency Department Use

  • 10mg IV provides similar analgesic efficacy to higher doses (15mg and 30mg) for acute pain in the emergency department 5
  • Effective for renal colic, migraine headache, musculoskeletal pain, and sickle cell crisis 4

Practical Application

  • Always use the lowest effective dose for the shortest duration
  • Oral formulation should not be given as an initial dose; only use as continuation therapy after IV/IM administration
  • Do not shorten the dosing interval of 4-6 hours
  • Avoid concurrent use with other NSAIDs to prevent increased risk of adverse effects 1, 2

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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