IM Ketorolac Dosing Frequency in Renal Impairment
For adults with impaired renal function, IM ketorolac should be administered at 15 mg every 6 hours, with a maximum daily dose of 60 mg and treatment duration not exceeding 5 days. 1
Standard Dosing Parameters
The FDA-approved dosing for IM ketorolac distinguishes clearly between patients with and without renal impairment 1:
Multiple-Dose Regimen (IM Administration)
Patients with renal impairment:
Patients <65 years without renal impairment:
Critical Safety Considerations
The 5-day maximum duration is non-negotiable because cumulative risks of gastrointestinal bleeding, renal impairment, and operative site bleeding increase substantially with prolonged therapy 2. This applies to all patients regardless of renal function.
Additional High-Risk Factors Requiring Dose Reduction
Beyond renal impairment, the following populations also require the reduced 15 mg every 6 hours dosing 1:
Contraindications in Renal Disease
Ketorolac should be avoided entirely in patients with 3:
- Severe renal impairment
- Compromised fluid status (hypovolemia must be corrected before administration) 1
Practical Implementation
Timing and administration:
- Administer slowly and deeply into the muscle 1
- Analgesic effect begins in approximately 30 minutes 1
- Maximum effect occurs 1-2 hours after dosing 1
- Duration of analgesic effect is typically 4-6 hours 1
For breakthrough pain: Do not increase the dose or frequency of ketorolac 1. Instead, consider supplementing with low doses of opioids unless contraindicated 1.
Common Pitfalls to Avoid
Do not exceed 5 days of treatment - Risk of serious adverse events increases markedly with longer duration, especially in elderly patients 4
Do not use higher doses in renal impairment - The 15 mg every 6 hours dose is already adjusted for reduced clearance 5
Monitor for acute renal failure - While usually reversible on drug discontinuation, this is a known risk with ketorolac 4
Assess bleeding risk - Ketorolac has reversible antiplatelet effects and the risk of gastrointestinal or operative site bleeding increases with high dosages used beyond 5 days 4