NSAID — Parenteral Analgesic
Pregnancy: Contraindicated in third trimester; avoid in first and second trimesters unless clearly necessary
Ketorolac Trometamol
Brand names: Toradol
Adult dose
Dose: 10-30 mg IV/IM every 4-6 hours
Route: Intravenous / Intramuscular
Frequency: Every 4-6 hours
Max: 90 mg/day (under 65); 60 mg/day (over 65 or renal impairment); maximum 5 days total
Restrict to maximum 5 days — GI and renal risks increase with duration. First dose IV: 30 mg; then 10-30 mg every 4-6 hours. Transition to oral NSAID as soon as possible
Paediatric dose
Dose: 0.5 mg/kg IV (max 15 mg per dose) mg/kg
Route: IV / IM
Frequency: Every 6 hours
Max: 60 mg/day
Child 16 years and over only — not licensed under 16. Seek specialist opinion for younger patients
Dose adjustments
Renal
Reduce to 10-15 mg every 4-6 hours (max 60 mg/day) in mild-moderate impairment; avoid if eGFR under 30
Hepatic
Use with caution in hepatic impairment
Paediatric weight-based calculator
Child 16 years and over only — not licensed under 16. Seek specialist opinion for younger patients
Clinical pearls
- Potent parenteral NSAID — equivalent analgesia to 6-12 mg morphine IM at a 30 mg dose, without opioid side effects; valuable opioid-sparing agent in perioperative care
- Maximum 5 days duration — GI and renal toxicity accumulate with duration; FDA and MHRA restrict duration; oral ibuprofen or diclofenac for continuation
- Platelet inhibition: reversible COX-1 inhibition — caution in procedures with bleeding risk; avoid in tonsillectomy (increased post-operative bleeding risk in children)
- Hypovolaemia is a contraindication — prostaglandin-dependent renal blood flow is critical in volume-depleted patients; ensure adequate hydration before and during use
- Strong evidence base for multimodal analgesia — combining ketorolac + paracetamol + opioid reduces morphine consumption by 30-50% post-operatively
Contraindications
- Active GI ulceration or bleeding
- Renal impairment (eGFR under 30)
- Coagulation disorders or anticoagulant use
- Hypovolaemia
- Established cardiovascular disease
- Third trimester of pregnancy
Side effects
- GI ulceration and bleeding (higher risk than other NSAIDs at analgesic doses)
- Renal impairment (AKI)
- Platelet inhibition and bleeding
- Hypersensitivity (aspirin-exacerbated respiratory disease)
Interactions
- Anticoagulants (significantly increased bleeding risk)
- Other NSAIDs (additive GI and renal toxicity)
- ACEi + diuretics (triple whammy AKI risk)
- Lithium (increased levels)
- Methotrexate (increased toxicity)
Monitoring
- Renal function (U&E)
- Signs of GI bleeding
- Blood pressure
- Fluid status
Reference: BNFc; BNF 90; Toradol SPC; PROSPECT Guidelines; MHRA 5-day restriction guidance. Verify against your local formulary and the latest BNF before prescribing.
Related
Curated clinical cross-links plus same-class fallbacks.
Pathways
- Major Trauma — Primary Survey (ATLS) · ATLS 10th Edition; JRCALC; NICE NG39
- Major Haemorrhage / Massive Transfusion · BCSH; RCOA; RCEM; RCS — BCSH Guidelines
- Burns — TBSA Estimation & Fluid Resuscitation · British Burn Association; EMSB; RCEM 2024
- Lower Gastrointestinal Bleed · NICE; BSG; ACPGBI — Commissioning Guide
- Acute Pancreatitis · NICE; IAP/APA; ACPGBI — CG104
- Hypertrophic Pyloric Stenosis · BAPS / RCPCH