What is the recommended dosage of Firocoxib (Equioxx) for pain and inflammation management in horses?

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Firocoxib (Equioxx) Dosage for Pain and Inflammation Management in Horses

The recommended dosage of firocoxib (Equioxx) for pain and inflammation management in horses is 0.1 mg/kg orally once daily for up to 14 days. 1, 2

Pharmacology and Administration Options

Firocoxib is a highly selective COX-2 inhibitor approved for treating musculoskeletal problems and lameness in horses with osteoarthritis. It has two FDA-approved formulations:

  • Oral paste formulation: 0.1 mg/kg once daily for up to 14 days 1
  • Injectable formulation: 0.09 mg/kg IV once daily for up to 5 days 1

Pharmacokinetic Properties

Firocoxib offers several advantageous pharmacokinetic properties that make it effective for equine pain management:

  • High bioavailability: ≥80% oral absorption 1
  • Wide distribution: Volume of distribution approximately 2 L/kg 1
  • Long half-life: Approximately 30-34 hours, allowing once-daily dosing 3
  • Steady state: Reached within 24-48 hours at recommended dosing 1

Loading Dose Option

For more rapid onset of action in acute pain situations:

  • A single loading dose of 0.3 mg/kg orally can be administered initially 1, 4
  • This approach establishes steady-state drug concentrations within 24 hours 1
  • After loading dose, continue with standard 0.1 mg/kg daily maintenance dose 4

Efficacy Considerations

  • Firocoxib's IC80 is 103 ng/mL in whole blood with an EC50 of 27 ng/mL 1
  • Clinical improvement in lameness and pain is typically observed within 7 days of starting treatment at the recommended dose 4
  • With a loading dose strategy, clinical improvement may be observed earlier (1-3 days) 4

Safety Profile

As a COX-2 selective NSAID, firocoxib offers a favorable safety profile compared to traditional NSAIDs:

  • COX-1/COX-2 IC50 ratio of 643 in horses, indicating high COX-2 selectivity 1
  • Reduced risk of gastrointestinal side effects compared to non-selective NSAIDs
  • Metabolized via dealkylation and glucuronidation to inactive metabolites 3
  • Primary elimination route is via urinary excretion 3

Practical Considerations

  • Formulation options: The equine paste formulation is specifically approved for horses, though studies show the canine tablet formulation has equivalent efficacy when dosed appropriately 5
  • Duration: Treatment should not exceed the FDA-approved 14-day treatment period without veterinary supervision 2
  • Monitoring: Regular assessment of clinical response and observation for any adverse effects is recommended

Potential Pitfalls and Caveats

  • Avoid exceeding recommended dosage or treatment duration to prevent potential adverse effects
  • As with all NSAIDs, monitor for signs of gastrointestinal disturbance, although risk is lower with COX-2 selective agents
  • Use with caution in horses with known renal, hepatic, or cardiovascular disease
  • Drug interactions with other medications should be considered, particularly with other NSAIDs or corticosteroids

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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