VetSheet

Toltrazuril

1-methyl-3-[3-methyl-4-[4-(trifluoromethylthio)phenoxy]phenyl]-1,3,5-triazine-2,4,6-trione

Antiprotozoal / AnticoccidialPODogsCatsBirdsReptilesSheep

Also known as: Baycox Β· Bay-Vi-9142 Β· Procox Β· toltrazurilo Β· toltrazurilum

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

10-20 mg/kg PO one timePOΒ· onceΒ· 1 dose
β€” πŸ•

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

Dosing by species

🌎 NA β€” North America🌍 EU β€” Europe

Dogs

IndicationDoseRouteFrequencyDurationRegion
Coccidiosis (Cystoisosporosis) prevention10-20 mg/kg PO one timePOonce1 dose🌎 NA
Coccidiosis15 mg/kg PO once dailyPOq24h3-6 days🌎 NA
Isospora spp. infections10-30 mg/kg PO once dailyPOq24h1-3 days🌎 NA
Coccidiosis20 mg/kg PO once dailyPOq24h3 days🌎 NA
Isospora spp. / Hepatozoon canis9-20 mg/kgPOonceSingle dose; further treatment is only indicated if oocyst shedding persists🌍 EU
  • Coccidiosis (Cystoisosporosis) prevention: Administer to all puppies at 3-4 weeks of age to help prevent problems associated with intestinal coccidiosis.
  • Isospora spp. / Hepatozoon canis: Standard dose is 9 mg/kg. Higher doses up to 20 mg/kg can be used if required.

Cats

IndicationDoseRouteFrequencyDurationRegion
Enteroepithelial cycle of toxoplasmosis (oocyst shedding)5-10 mg/kg PO once dailyPOq24h2 days🌎 NA
Coccidiosis30 mg/kg PO once dailyPOq24h2-3 days🌎 NA
Coccidiosis20 mg/kg PO once dailyPOq24h3 days🌎 NA
Isospora spp.9-20 mg/kgPOonceSingle dose; further treatment is only indicated if oocyst shedding persists🌍 EU
  • Isospora spp.: Not authorized for use in cats but appears to be effective. Standard dose is 9 mg/kg. Higher doses up to 20 mg/kg can be used if required.

Birds

IndicationDoseRouteFrequencyDurationRegion
Coccidiosis in raptors7 mg/kg PO once dailyPOq24h2-3 days🌎 NA

Reptiles

IndicationDoseRouteFrequencyDurationRegion
Parasitism in Bearded Dragons5-15 mg/kg PO once dailyPOq24h3 days🌎 NA

Sheep

IndicationDoseRouteFrequencyDurationRegion
Ovine coccidiosis (Eimeria ovinoidalis)20 mg/kg PO oncePOonce1 dose🌎 NA
  • Ovine coccidiosis (Eimeria ovinoidalis): Controlled study comparing efficacy against diclazuril.

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

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Overview

Toltrazuril is a triazinone (triazine) antiprotozoal agent primarily labeled for treating coccidiosis in poultry and swine in Europe. In companion animal medicine, it is utilized off-label as an alternative treatment for various protozoal infections.

​Key Uses:​

  • Coccidiosis in dogs and cats
  • Isospora or Hepatozoon infections
  • Oocyst shedding stage of toxoplasmosis in cats
  • Overwhelming parasitic loads in reptiles (e.g., Bearded Dragons)

​Clinical Pearls:​

  • Toltrazuril is the parent compound to ponazuril (toltrazuril sulfone), which is more commonly used and available in the US.
  • While it can induce excellent initial clinical responses in dogs with American canine hepatozoonosis (ACH), it cannot completely eliminate the parasites, and remission is usually transient.
  • ​Regulatory Note:​ It is not commercially available in the USA and must be legally imported for compassionate use.

Mechanism of action

The exact mechanism of action is not completely understood, but as a triazinone derivative, it acts on all intracellular developmental stages of coccidia.

  • ​Pathway:​ It appears to inhibit protozoal enzyme systems β†’ disrupts the division of the nucleus and the activity of the mitochondria β†’ impairs the respiratory metabolism of the parasite β†’ protozoal death.
  • It is rapidly metabolized in the liver to its active sulfone derivative, ponazuril.

Safety & warnings

Contraindications

  • Known hypersensitivity to toltrazuril or other triazinone antiprotozoals (e.g., ponazuril, diclazuril)
  • Puppies or kittens < 2 weeks of age
  • Animals weighing < 0.4 kg

Adverse effects

  • Generally well tolerated in birds
  • Potential gastrointestinal upset in mammals
  • Blisters on nose and mouth (extrapolated from ponazuril use in horses)
  • Rash or hives (extrapolated from ponazuril use in horses)
  • Mild diarrhoea
  • Vomiting

Precautions

Use with caution in pregnant or lactating animals, as no reproductive or nursing safety information is available; weigh potential risks versus benefits. The principle metabolite persists in the environment and can contaminate groundwater, though the risk is considered minimal when used in companion animals.

Drug interactions

EmodepsideMinor

Frequently formulated together; no negative interactions known between the two, but refer to emodepside monograph for its specific interactions.

Monitoring

  • Clinical efficacy (resolution of clinical signs, negative fecal tests)
  • Fecal flotation to monitor for resolution of oocyst shedding
  • Resolution of clinical signs (e.g., diarrhea)

Pharmacokinetics

Half-life

CatsUnknown, presumed longDogsApproximately 114 hours

Absorption

About 50% absorbed after oral consumption in poultry.

Distribution

Highest concentrations are found in the liver.

Metabolism

Rapidly metabolized into the sulfone derivative (ponazuril).

Elimination

Excreted primarily in the feces, with a very long elimination half-life.

Overdose

Very limited information is available.

  • ​Horses:​ Doses up to 10X were tolerated without significant adverse effects.
  • ​Poultry:​ 5X overdoses have been tolerated without clinical signs. Decreased water intake has been observed if overdoses are greater than 5X.

Available products

Formulations

  • 2.5% (25 mg/mL) oral solution
  • 18 mg/ml oral suspension (formulated with emodepside)

Veterinary

  • Baycox 2.5% Solution (25 mg/mL) (Available in Europe; None in the USA)
  • Procox oral suspension (18 mg/ml toltrazuril + 0.9 mg/ml emodepside)
  • Baycox (various concentrations for livestock, sometimes used off-label)

Regulatory status

European Unionβœ“ ApprovedPrescription onlyEMA
πŸ• Dogs

Approved as Procox (combination with emodepside) for dogs.

United Kingdomβœ“ ApprovedPrescription onlyVMD
πŸ• Dogs

POM-V. Available on a named patient basis in the UK.

No regulatory data for: πŸ‡ΊπŸ‡Έ US Β· πŸ‡­πŸ‡° HK Β· πŸ‡ΉπŸ‡Ό TW Β· πŸ‡―πŸ‡΅ JP Β· πŸ‡°πŸ‡· KR Β· πŸ‡¦πŸ‡Ί AU

Storage & stability

Store the 2.5% solution at temperatures at 25Β°C or below. Dilutions in drinking water more concentrated than 1:1000 (1 mL of the 2.5% solution to 1 liter of water) may precipitate. After dilution, the resulting solution is stable for 24 hours. Discard medicated drinking water not consumed after 24 hours.

Client information

​Safety Warning:​ Avoid direct contact with this medication. The manufacturer recommends wearing synthetic rubber gloves when handling the 2.5% solution. Wash exposed skin thoroughly after use.

  • Administer exactly as directed by your veterinarian.
  • If diluting the medication in drinking water, discard any medicated water that is not consumed within 24 hours.

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.