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Antifibrinolytic agent (haemostatic) Pregnancy: Use with caution — limited data; appears safe in short courses for menorrhagia but avoid in first trimester if possible.

Tranexamic Acid 500mg Tablets (Epistaxis)

Brand names: Cyklokapron, Tranexamic acid generic

Adult dose

Dose: Oral: 1–1.5 g (2–3 × 500 mg) three times daily for up to 5–7 days. Topical: 500 mg/5 mL solution applied to nasal mucosa as soaked gauze/pledget
Route: Oral or topical intranasal
Frequency: Three times daily (oral); as required (topical)
Max: 4.5 g/day (oral)
Epistaxis: oral tranexamic acid 1 g TDS for 5–7 days as adjunct to anterior nasal packing or cauterisation. Topical use: 500 mg/5 mL solution (injectable preparation used off-label intranasally) — soaked pledget or spray; evidence shows efficacy comparable to anterior packing for anterior epistaxis. Particularly useful in: hereditary haemorrhagic telangiectasia (HHT/Osler-Weber-Rendu), warfarin-associated epistaxis.

Paediatric dose

Dose: 15 mg/kg
Route: Oral
Frequency: Three times daily
Max: 1.5 g/dose
Children (>1 year): 15–25 mg/kg three times daily (max 1.5 g per dose). Used in von Willebrand disease and HHT-related epistaxis in children. Topical application in children: specialist guidance.

Dose adjustments

Renal

eGFR 40–60: 1 g twice daily. eGFR 20–40: 500 mg twice daily. eGFR 10–20: 500 mg once daily. Avoid if eGFR <10.

Hepatic

No dose adjustment required.

Paediatric weight-based calculator

Children (>1 year): 15–25 mg/kg three times daily (max 1.5 g per dose). Used in von Willebrand disease and HHT-related epistaxis in children. Topical application in children: specialist guidance.

Clinical pearls

  • Topical tranexamic acid is evidence-based for acute anterior epistaxis — comparable to anterior packing and less traumatic
  • Particularly useful in anticoagulated patients (warfarin, DOAC) — reduces bleeding without reversing anticoagulation
  • HHT (Osler-Weber-Rendu): oral tranexamic acid is first-line pharmacological therapy for recurrent epistaxis
  • Widely used in trauma and surgery — ENT application is one of many uses
  • Ensure patient has no contraindications to antifibrinolytics before prescribing (check thrombosis history)

Contraindications

  • History of thromboembolic disease (DVT, PE, arterial thrombosis) — relative contraindication
  • Haematuria originating from upper urinary tract (risk of obstructive clot in ureters)
  • Subarachnoid haemorrhage (risk of cerebral vasospasm)
  • Hypersensitivity to tranexamic acid

Side effects

  • Nausea, vomiting, diarrhoea
  • Thromboembolic events (rare at low doses; increased risk with high doses / predisposed patients)
  • Hypotension with rapid IV administration
  • Seizures (rare — CNS effect at very high doses or IV)
  • Visual disturbance (rare)

Interactions

  • Hormonal contraceptives — additive thrombotic risk
  • Factor IX complex / anti-inhibitor coagulant concentrates — avoid combination (thrombosis risk)
  • All-trans retinoic acid (ATRA) — increased thrombotic risk in APL treatment

Monitoring

  • Epistaxis resolution
  • Coagulation screen if recurrent epistaxis or anticoagulated
  • Renal function

Reference: BNFc; BNF; NICE CKS Epistaxis; ENT-UK Epistaxis Guidelines; BMJ Evidence on Topical TXA. Verify against your local formulary and the latest BNF before prescribing.

Related

Curated clinical cross-links plus same-class fallbacks.