VetSheet

Etodolac

Indole acetic acid derivative

Also known as: EtoGesic · Lodine · AY-24236 · etodolacum · etodolic acid · Acudor · Articulan · Dualgan · Eccoxolac · Edolan · Elderin · Etonox · Etopan · Flancox · Hypen · Lodot · Lonine · Metazin · Sodolac · Ultradol · Zedolac

Reviewed by the VetSheet Veterinary TeamUpdated Apr 5, 2026Evidence-based veterinary reference

10-15 mg/kgPO· once daily
🐕

Doses are a clinical reference for licensed veterinary professionals. Always confirm against the current label and the individual patient.

Dosing by species

🌎 NA — North America🌍 EU — Europe

Dogs

IndicationDoseRouteFrequencyDurationRegion
Treatment of pain and inflammation associated with osteoarthritis10-15 mg/kgPOonce daily🌎 NA
Treatment of pain and inflammation associated with osteoarthritis10-15 mg/kgSConce🌎 NA
  • Treatment of pain and inflammation associated with osteoarthritis: Dogs less than 5 kg cannot be accurately dosed with EtoGesic tablets. Adjust dose to obtain satisfactory response, but do not exceed 15 mg/kg. For long-term therapy, reduce dose level to minimum effective dosage.
  • Treatment of pain and inflammation associated with osteoarthritis: Administer as a dorsoscapular subcutaneous injection. If needed, daily doses of tablets may begin 24 hours after the last injectable treatment. Use alternate injection sites.

Doses are a clinical reference for licensed veterinary professionals. Always confirm against the current label and the individual patient.

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Overview

Etodolac is a non-steroidal anti-inflammatory drug (NSAID) primarily utilized in veterinary medicine for the management of pain and inflammation associated with osteoarthritis in dogs.

  • Available in both oral tablet and injectable formulations.
  • Characterized by a relatively long half-life in dogs, allowing for convenient once-daily dosing.
  • Clinical Pearl: While effective, etodolac has a narrower therapeutic index compared to some newer veterinary NSAIDs (e.g., carprofen, meloxicam), meaning precise dosing is critical to avoid gastrointestinal toxicity. Doses as little as 2.7X the therapeutic dose can produce gastrointestinal lesions.

Mechanism of action

Etodolac exerts its analgesic, anti-inflammatory, and antipyretic effects primarily by inhibiting the ​cyclooxygenase (COX)​ enzymes.

  • Arachidonic Acid → Prostaglandins: By blocking COX, etodolac prevents the conversion of arachidonic acid into pro-inflammatory prostaglandins.
  • It is generally considered a COX-1 sparing drug rather than highly COX-2 selective in dogs. In horses, it does not exhibit much COX-2 selectivity.
  • Additionally, etodolac inhibits macrophage chemotaxis, which further blunts the inflammatory cascade at the site of tissue injury.

Safety & warnings

Contraindications

  • Known hypersensitivity to etodolac
  • Dogs less than 12 months of age
  • Breeding, pregnant, or lactating dogs (safe use not established)
  • Cats (highly sensitive to toxicity)

Adverse effects

  • Vomiting
  • Regurgitation
  • Diarrhea
  • Lethargy
  • Hypoproteinemia
  • Urticaria
  • Behavioral changes
  • Inappetence
  • Hepatotoxicity (rare)
  • Nephrotoxicity (rare)
  • Localized pain or tissue reactions at injection site
  • Decreased total serum T4
  • Keratoconjunctivitis sicca (KCS)

Precautions

Use with caution in dogs with preexisting or occult GI, hepatic, renal, cardiovascular, or hematologic abnormalities as NSAIDs may exacerbate these conditions.

Important: Patients may be more susceptible to renal injury from etodolac if they are dehydrated, on diuretics, or have preexisting renal, hepatic, or cardiovascular dysfunction.

Terminate therapy if inappetence, vomiting, fecal abnormalities, or anemia are observed.

Drug interactions

ACE Inhibitors (enalapril, benazepril)

May reduce antihypertensive effects and increase the risk for renal injury.

Aspirin

May decrease etodolac plasma levels and increase likelihood of GI adverse effects (blood loss). Concomitant use is not recommended.

Cyclosporine

May increase cyclosporine blood levels and increase the risk for nephrotoxicity.

Digoxin

May increase serum levels of digoxin. Use with caution in severe cardiac failure.

Furosemide & other diuretics

May reduce the saluretic and diuretic effects of furosemide.

Methotrexate

Serious toxicity has occurred with concomitant NSAID use.

Nephrotoxic agents (amphotericin B, aminoglycosides, cisplatin)

Potential for increased risk of nephrotoxicity.

Phenobarbital

May increase the metabolism of etodolac in dogs.

Probenecid

May cause a significant increase in serum levels and half-life of etodolac.

Warfarin

May increase the risk for bleeding.

Monitoring

  • Baseline physical exam, CBC, Serum chemistry panel (liver and renal function), and Urinalysis
  • Reassess liver enzymes at one week of therapy
  • Tear production (Schirmer Tear Test) prior to and during therapy due to KCS risk
  • Clinical efficacy (pain scoring)
  • Signs of adverse reactions: inappetence, vomiting, melena, diarrhea, PU/PD, jaundice, lethargy

Pharmacokinetics

Half-life

Horses2.5-3 hoursDogs8-12 hours

Absorption

Rapidly and nearly completely absorbed after oral administration. Food may alter the rate, but not the extent, of absorption. Peak serum levels occur about 2 hours post dosing. Oral bioavailability in horses is about 77%.

Distribution

Highly bound to serum proteins. In horses, volume of distribution is 0.29 L/kg.

Metabolism

Glucuronide conjugates have been detected in the bile but not the urine.

Elimination

Primarily excreted via the bile into the feces. Rate of enterohepatic circulation may be affected by the presence of food in the gut.

Overdose

Etodolac has a relatively narrow therapeutic window in dogs.

  • ​2.7X overdose (40 mg/kg/day)​: Can cause GI ulcers, weight loss, emesis, and local occult blood.
  • ​5.3X overdose (80 mg/kg/day)​: Highly lethal; caused death or moribund state secondary to severe GI ulceration in safety studies.
  • Feline Toxicity: Cats are highly sensitive. Exposures have resulted in acute renal failure, anorexia, collapse, hyperkalemia, and hypersalivation.

Treatment: Decontamination with emetics and/or activated charcoal may be appropriate for acute ingestions. Use gastrointestinal protectants for expected GI effects. If renal effects are anticipated, aggressive fluid diuresis is warranted.

Available products

Formulations

  • Oral tablets
  • Subcutaneous injection

Veterinary

  • Etodolac Scored Tablets: 150 mg & 300 mg (EtoGesic)
  • Etodolac Injection 10% (100 mg/mL) in 50 mL vials (EtoGesic Injectable)

Human-labeled

  • Etodolac Tablets: 400 mg & 500 mg
  • Etodolac Capsules: 200 mg & 300 mg
  • Etodolac Extended-release tablets: 400 mg, 500 mg & 600 mg

Regulatory status

No regulatory data for: 🇺🇸 US · 🇪🇺 EU · 🇬🇧 UK · 🇭🇰 HK · 🇹🇼 TW · 🇯🇵 JP · 🇰🇷 KR · 🇦🇺 AU

Storage & stability

Veterinary tablets should be stored at controlled room temperature (15-30°C). Injection should be stored at or below 77°F (25°C).

Client information

Administration: Give the medication exactly as prescribed by your veterinarian. It is often best given with food to reduce the chance of stomach upset.

Watch for Side Effects: Stop the medication immediately and contact your veterinarian if your dog experiences:

  • Vomiting or regurgitation
  • Diarrhea or dark, tarry stools (melena)
  • Loss of appetite or extreme lethargy
  • Increased thirst or urination

Eye Health: Rarely, this drug can cause "dry eye" (keratoconjunctivitis sicca). Watch for excessive squinting, redness, or thick, sticky eye discharge.

WARNING: Never give this medication to cats or other pets, as it can be highly toxic and potentially fatal to them. Keep out of reach of all animals and children.

VetSheet drug reference is intended for licensed veterinary professionals as a clinical decision-support aid, not a substitute for professional judgement or the manufacturer’s current label.