What are the guidelines for using Toradol (Ketorolac) for pain management?

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Last updated: June 10, 2025View editorial policy

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From the Guidelines

Toradol (ketorolac) should be used for short-term management of moderate to severe acute pain only, with treatment limited to a maximum of 5 days due to increased risk of serious side effects with longer use. The recommended dosage for adults is 60 mg IM every 15 to 30 minutes, with a maximal dosage of 120 mg per day, as stated in the study 1. According to the guidelines, Toradol is contraindicated in patients with aspirin/NSAID-induced asthma, pregnancy, and cerebrovascular hemorrhage 1. It should be used cautiously in patients with a history of peptic ulcer disease, risk of bleeding, or renal impairment. Patients should be monitored for gastrointestinal bleeding, renal dysfunction, and cardiovascular events during treatment.

Key Considerations

  • The use of Toradol should be limited to a maximum of 5 days due to the increased risk of serious side effects with longer use 1.
  • The recommended dosage for adults is 60 mg IM every 15 to 30 minutes, with a maximal dosage of 120 mg per day 1.
  • Toradol is contraindicated in patients with aspirin/NSAID-induced asthma, pregnancy, and cerebrovascular hemorrhage 1.
  • Patients should be monitored for gastrointestinal bleeding, renal dysfunction, and cardiovascular events during treatment.

Alternative Options

  • Other NSAIDs, such as ibuprofen or naproxen sodium, may be considered for patients who are at high risk for renal, GI, cardiac toxicities, thrombocytopenia, or bleeding disorder 1.
  • Opioid analgesics are safe and effective alternative analgesics to NSAIDs, especially for patients with a history of peptic ulcer disease or risk of bleeding 1.

Monitoring and Precautions

  • Patients should be monitored for gastrointestinal bleeding, renal dysfunction, and cardiovascular events during treatment.
  • Toradol should be used cautiously in elderly patients, typically at reduced doses.
  • Patients with a history of peptic ulcer disease, risk of bleeding, or renal impairment should be closely monitored during treatment.

From the FDA Drug Label

DOSAGE AND ADMINISTRATION Carefully consider the potential benefits and risks of ketorolac tromethamine tablets and other treatment options before deciding to use ketorolac tromethamine tablets. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals In adults, the combined duration of use of IV or IM dosing of ketorolac tromethamine and ketorolac tromethamine tablets is not to exceed 5 days.

INDICATIONS AND USAGE Carefully consider the potential benefits and risks of Ketorolac Tromethamine Tablets USP and other treatment options before deciding to use Ketorolac Tromethamine Tablets USP. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals Acute Pain in Adult Patients Ketorolac Tromethamine Tablets USP are indicated for the short-term (≤ 5 days) management of moderately severe acute pain that requires analgesia at the opioid level, usually in a postoperative setting

The guidelines for using Toradol (Ketorolac) for pain management are as follows:

  • Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals.
  • The combined duration of use of IV or IM dosing of ketorolac tromethamine and ketorolac tromethamine tablets is not to exceed 5 days.
  • Therapy should always be initiated with IV or IM dosing of ketorolac tromethamine and Ketorolac Tromethamine Tablets USP are to be used only as continuation treatment, if necessary.
  • Patients should be switched to alternative analgesics as soon as possible, but Ketorolac Tromethamine Tablet USP therapy is not to exceed 5 days.
  • The recommended dosing instructions are:
    • Patients age 17 to 64: 20 mg PO once followed by 10 mg q4 to 6 hours prn not > 40 mg/day
    • Patients age ≥ 65, renally impaired, and/or weight < 50 kg (110 lbs): 10 mg PO once followed by 10 mg q4 to 6 hours prn not > 40 mg/day 2 2

From the Research

Guidelines for Using Toradol (Ketorolac) for Pain Management

  • Toradol, also known as Ketorolac, is a nonsteroidal anti-inflammatory drug (NSAID) used for pain management 3.
  • The guidelines for using Toradol for pain management include administering it at a dose of 10mg, 15mg, or 30mg intravenously, with similar analgesic efficacy demonstrated at all three doses 3.
  • Toradol is commonly used in the emergency department for treating acute pain, with a numeric rating scale score greater than or equal to 5 3.
  • Patients with peptic ulcer disease, gastrointestinal hemorrhage, renal or hepatic insufficiency, allergies to NSAIDs, pregnancy or breastfeeding, and certain blood pressure or pulse rate conditions should be excluded from using Toradol 3.
  • The primary outcome of using Toradol is pain reduction at 30 minutes, with rescue analgesia administered if necessary 3.
  • Adverse effects of Toradol include dizziness, nausea, and headache, with similar rates of adverse effects per group 3.

Comparison with Other Pain Management Options

  • Tramadol, another pain management option, has a unique adverse effect profile due to its serotonin and norepinephrine reuptake inhibitory effects 4.
  • Tramadol-induced serotonin syndrome and seizures can be effectively treated by administering benzodiazepines, providing supportive care, and discontinuing tramadol and other contributing agents 4.
  • Other pain management options, such as ibuprofen/acetaminophen fixed-dose combinations, have been shown to be effective alternatives to opioids in acute pain settings 5.
  • Long QT syndrome is a cardiac repolarization disorder that can be associated with certain pain medications, including NSAIDs, opioids, and anticonvulsive and antidepressant drugs 6.

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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