BLACK BOX WARNING
- GI toxicity
- renal toxicity
- cardiovascular thrombotic events
- risk of bleeding
- use limited to 5 days
- contraindicated in labor/delivery and perioperative CABG
ketorolac
Brand: Toradol
⚠ BBW Beers Criteria Prototype: ibuprofen
Drug Class: nonsteroidal anti-inflammatory drug (NSAID)
Drug Family: NSAID
Subclass: non-selective COX inhibitor (pyrrolizine carboxylic acid)
Organ Systems: cnsmusculoskeletal
Mechanism of Action
Potent non-selective COX inhibitor with analgesic potency comparable to opioids at recommended doses; available in IV/IM/oral/intranasal formulations. Inhibits prostaglandin synthesis to produce analgesia without direct opioid receptor activity.
COX-1COX-2
Indications
- moderate to severe pain (short-term, up to 5 days only)
- post-operative pain
- renal colic
Contraindications
- active peptic ulcer
- renal impairment
- cerebrovascular bleeding
- third trimester pregnancy
- pre- or intraoperative use when hemostasis is critical
- labor and delivery
Adverse Effects
Common
- nausea
- dyspepsia
- GI pain
- drowsiness
- injection site pain (IM)
Serious
- GI bleeding/ulceration (higher risk than oral NSAIDs due to parenteral route and potency)
- AKI
- bleeding (impairs platelet function)
Pharmacokinetics (ADME)
| Absorption | IV: complete; IM: complete; oral: ~80%; intranasal: ~36% |
| Distribution | protein binding >99%; Vd ~0.23 L/kg |
| Metabolism | hepatic glucuronidation and para-hydroxylation |
| Excretion | renal (92%) |
| Half-life | 5-6 hours |
| Onset | IV: 10-15 minutes; IM: 30-60 minutes |
| Peak | IV: 1-2 hours; IM: 45 minutes |
| Duration | 4-6 hours |
| Protein Binding | >99% |
| Vd | 0.23 L/kg |
Drug Interactions
| Drug / Agent | Mechanism | Severity |
|---|---|---|
| anticoagulants | additive bleeding risk; major concern | major |
| ACE inhibitors/ARBs | AKI risk; antihypertensive antagonism | major |
| probenecid | inhibits ketorolac renal clearance; increase in ketorolac levels | major |
Nursing Considerations
- Maximum treatment duration is 5 days total (IV + IM + oral combined); document start date and calculated end date on the medication administration record.
- Parenteral ketorolac provides opioid-comparable analgesia for moderate-severe pain; it is an important opioid-sparing or opioid-alternative analgesic in appropriate patients.
- IM injection must be given deep into large muscle mass (ventrogluteal or vastus lateralis); painful injection if given subcutaneously.
- Absolute contraindication in third trimester pregnancy and active bleeding; verify pregnancy status and recent labs before administration.
Clinical Pearls
- Ketorolac is the only parenteral (IV/IM) NSAID available in the US, occupying a unique niche as a non-opioid parenteral analgesic for moderate-severe pain when opioids are undesirable.
- The 5-day treatment limit is not merely a caution — it is a hard FDA requirement based on clinical trial data showing sharply increased GI toxicity beyond 5 days; prescriptions should not exceed this duration.
Safety Profile
Pregnancy contraindicated
Lactation use-with-caution
Renal Adjustment Required
Hepatic Adjustment Required
TDM Not required
Concordance Terms
Cross-referenced clinical concepts — click any term to see all content where it appears.