Ketorolac IV Dosing
For adults under 65 years, administer 30 mg IV every 6 hours (maximum 120 mg/day); for adults ≥65 years, renally impaired patients, or those weighing <50 kg, reduce to 15 mg IV every 6 hours (maximum 60 mg/day), with treatment duration not exceeding 5 days. 1
Standard Dosing by Patient Population
Adults <65 Years (Normal Renal Function, Weight ≥50 kg)
- Multiple-dose regimen: 30 mg IV every 6 hours, maximum 120 mg/day 1
- Single-dose regimen: 30 mg IV once 1
- IV bolus must be administered over at least 15 seconds 1
High-Risk Populations (≥65 Years, Renal Impairment, or <50 kg)
- Multiple-dose regimen: 15 mg IV every 6 hours, maximum 60 mg/day 1
- Single-dose regimen: 15 mg IV once 1
- These reduced doses are mandatory, not optional, as elderly patients have markedly increased risk of adverse events with higher doses 2
Critical Dosing Principles
Analgesic Ceiling Effect
- Doses above 10 mg IV provide no additional analgesic benefit 3
- A 2017 randomized controlled trial demonstrated equivalent pain reduction at 30 minutes with 10 mg, 15 mg, and 30 mg IV doses (mean pain score reductions of 2.6,2.5, and 3.0 respectively, with overlapping confidence intervals) 3
- Despite this ceiling effect, FDA-approved dosing remains 15-30 mg based on patient characteristics 1
Duration Limits
- Maximum treatment duration: 5 days 1, 4
- Risk of serious adverse events increases dramatically with prolonged therapy beyond 5 days, especially in elderly patients 2
- Switch to alternative analgesics as soon as clinically feasible 1
Absolute Contraindications
Ketorolac is contraindicated in patients with: 4, 1
- Active or history of peptic ulcer disease or GI bleeding
- Aspirin/NSAID-induced asthma
- Cerebrovascular bleeding or hemorrhagic stroke
- Advanced renal impairment or risk of renal failure
- Concurrent anticoagulant or antiplatelet therapy
- Pregnancy (risk of fetal harm and premature closure of ductus arteriosus)
- Labor and delivery
- Age >60 years with significant alcohol use or hepatic dysfunction 5
Renal Impairment Considerations
Patients with Compromised Renal Function
- Use 15 mg IV every 6 hours (maximum 60 mg/day) 1
- Correct hypovolemia prior to administration 1
- Avoid in patients with creatinine clearance <30 mL/min when possible 4
- Never combine with other nephrotoxic agents (aminoglycosides, NSAIDs, ACE inhibitors) as renal impairment occurs in 8.7% of patients receiving concurrent nephrotoxic therapy 6
Required Monitoring
Baseline Assessment
Before initiating ketorolac, obtain: 4, 5
- Blood pressure
- BUN and creatinine
- Liver function tests
- Complete blood count
- Fecal occult blood test (in high-risk patients)
Discontinuation Criteria
Stop ketorolac immediately if: 5, 4
- BUN or creatinine doubles from baseline
- Hypertension develops or worsens
- Liver function tests increase >3× upper limit of normal
- Any signs of GI bleeding occur
Clinical Pearls and Pitfalls
Common Prescribing Errors to Avoid
- Never combine ketorolac with other NSAIDs (including ibuprofen, naproxen) - toxicities are additive without additional analgesic benefit, significantly increasing risks of GI bleeding, renal failure, and cardiovascular events 6
- Wait 6-8 hours after last ibuprofen dose before administering ketorolac to allow adequate drug clearance 6
- Do not increase dose or frequency for breakthrough pain; instead, add low-dose opioids if not contraindicated 1
Opioid-Sparing Effects
- Ketorolac combined with opioids reduces opioid requirements by 25-50% 5, 7
- This combination may decrease opioid-related adverse events and shorten hospital stay 7
- Consider multimodal analgesia rather than escalating ketorolac dose 5
Onset and Duration
- Analgesic effect begins in approximately 30 minutes 1
- Maximum effect occurs at 1-2 hours after administration 1
- Duration of analgesia is typically 4-6 hours 1
- Onset may be delayed compared to opioids, but duration is often longer 7
Special Populations
Postoperative patients: Ketorolac 15-30 mg IV every 6 hours for maximum 5 days is appropriate for post-cesarean delivery and other surgical procedures, barring contraindications 4
Breastfeeding: Not a contraindication when used as directed in the immediate postpartum period 4
Pediatric patients: Not addressed in the provided evidence for IV dosing; consult pediatric-specific guidelines 8