Diminazene Aceturate and Diminazene Diaceturate (Berenil) for Animals

Diminazene Aceturate and Diminazene Diaceturate (Berenil)

Diminazene Aceturate and Diminazene Diaceturate (Berenil) is used in veterinary medicine for babesiosis.

Diminazene aceturate is also termed diminazene diaceturate; the salt amount must remain distinct from an unspecified free-base amount.

Group

Diamidine antiprotozoal

Mechanism of Action

Interferes with protozoal nucleic-acid function.

Dose Rates

Dog

Use / stageDoseRouteScheduleInstructions
BabesiosisReference onlyIMSource regimen: 3.5–5 mg/kg every 12 hours for two doses. Salt basis is not specified consistently; resolve it before using a diaceturate-strength calculator.
African trypanosomiasis3.6–7 mg/kgIMEvery 336 hRepeat only as needed for relapse or reinfection; neurologic toxicity risk increases with cumulative exposure.

Cat

Use / stageDoseRouteScheduleInstructions
Historical antiprotozoal regimensReference onlyIMReported courses include 4 mg/kg daily for five doses; experimental T. evansi treatment used 3.5 mg/kg daily for five days. Cytauxzoon reports used 2 mg/kg for two injections within one week without parasite eradication. Toxicity and lack of consistent success make these unsuitable as routine feline regimens.
Cytauxzoonosis2 mg/kgIMEvery 168 hTwo doses one week apart. Historical treatment with poor success; monitor closely for toxicity.
Cytauxzoonosis3–5 mg/kgIMOnceHistorical alternative with poor treatment success; not evidence of reliable cure.

Cattle

Use / stageDoseRouteScheduleInstructions
Babesiosis or trypanosomiasisReference onlyIMSource range 3.5–7 mg/kg; babesia studies also cite 3–5 mg/kg. Salt basis and repeat schedule are not fully specified.
Susceptible protozoal infection3.5 mg/kgIMOnceMaximum 4 g/dose; Diminazene aceturate/diaceturate basis; response depends on organism susceptibility. The source mentions escalation up to 8 mg/kg but does not define organism-specific selection.

Horse

Use / stageDoseRouteScheduleInstructions
Equine piroplasmosis3.5–5 mg/kgIMEvery 48 hUp to 4 days; Diaceturate; two treatments only. Severe local reactions can occur.
Babesiosis3–5 mg/kgIMEvery 12 hUp to 1 days; Diaceturate; two treatments only. A distinct study used 5 mg/kg twice 24 hours apart for B. caballi; do not merge schedules.
Susceptible protozoal infection3.5 mg/kgIMOnceMaximum 4 g/dose; Diminazene aceturate/diaceturate basis; response depends on organism susceptibility. The source mentions escalation up to 8 mg/kg but does not define organism-specific selection.

Sheep

Use / stageDoseRouteScheduleInstructions
Susceptible protozoal infection3.5 mg/kgIMOnceMaximum 4 g/dose; Diminazene aceturate/diaceturate basis; response depends on organism susceptibility. The source mentions escalation up to 8 mg/kg but does not define organism-specific selection.

Goat

Use / stageDoseRouteScheduleInstructions
Susceptible protozoal infection3.5 mg/kgIMOnceMaximum 4 g/dose; Diminazene aceturate/diaceturate basis; response depends on organism susceptibility. The source mentions escalation up to 8 mg/kg but does not define organism-specific selection.

Indications

  • Babesiosis
  • Trypanosomiasis
  • Equine piroplasmosis

Contraindications

  • Not recommended in cats because of toxicity and inconsistent efficacy.
  • Camelids are highly susceptible to diminazene toxicity; avoid use when the preparation contraindicates camelids.

Interactions

  • No specific interactions identified in the supplied monograph.

Adverse effects

  • Painful injection and muscle injury
  • Salivation, nausea, vomiting and hepatic enzyme elevations in cats

Toxicity

Neurologic and systemic toxicity may be severe; avoid repeat dosing outside a defined regimen.

Preparations

PreparationFormStrengthRoute
Prozomin injection
Diminazene diaceturate 70 mg/mL plus phenazone 375 mg/mL. Deep IM; calculations use only the diminazene component.
Injectiondiminazene diaceturate 70 mg / mL + phenazone 375 mg / mLIM

Monitoring and Administration

Monitor neurologic status, CBC, hepatic function and injection sites. Narrow therapeutic margin limits empirical escalation.

Aceturate/diaceturate identity and dose basis must be confirmed for the actual preparation; do not convert using an assumed salt factor.

Monitor serial CBC, renal and hepatic indices and potassium during severe babesiosis. PCR at 60 and 90 days after therapy was proposed to assess B. gibsoni clearance; clinical recovery does not establish eradication.

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