VetSheet

Imidocarb

Imidocarb dipropionate

AntiprotozoalIMSCDogsCatsHorsesSheep

Also known as: Imizol ยท Imidocarb dipropionate ยท Imidocarb hydrochloride ยท 4A65 ยท Imidocarbum

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

6.6 mg/kgIM or SCยท repeat dose in 2 weeks
โ€” ๐Ÿ•

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

Dosing by species

๐ŸŒŽ NA โ€” North America๐ŸŒ EU โ€” Europe

Dogs

IndicationDoseRouteFrequencyDurationRegion
Babesiosis6.6 mg/kgIM or SCrepeat dose in 2 weeksโ€”๐ŸŒŽ NA
Babesiosis5-6.6 mg/kgIM or SCrepeat in 14 daysโ€”๐ŸŒŽ NA
Ehrlichiosis (Severe cases)5 mg/kgSCsingle injection or two injections 15 days apartโ€”๐ŸŒŽ NA
Hepatozoonosis (H. canis)5 mg/kgIM or SCevery 14 daysuntil parasitemia clears๐ŸŒŽ NA
Treatment of Babesia canis infection6.6 mg/kgIM/SConce, repeated in 2-3 weeks2 doses total๐ŸŒ EU
  • Babesiosis: Alternatively, 7.5 mg/kg IM or SC once. A single dose of 6 mg/kg the day following a dose of diminazene at 3.5 mg/kg has also been shown to clear the infection.
  • Ehrlichiosis (Severe cases): Given with doxycycline at 10 mg/kg/day for 28 days. Note: Imidocarb alone is not effective in clearing E. canis.
  • Hepatozoonosis (H. canis): Usually 1-2 injections are sufficient.
  • Treatment of Babesia canis infection: Dose based on imidocarb dipropionate (121.15 mg/ml). Premedication with atropine (0.05 mg/kg) to minimize side effects is highly recommended.

Cats

IndicationDoseRouteFrequencyDurationRegion
Cytauxzoon felis3-4 mg/kgIMrepeated 7 days after initial doseโ€”๐ŸŒŽ NA
Cytauxzoon felis5 mg/kgIMonce and then 14 days laterโ€”๐ŸŒŽ NA
Feline hemoplasmosis (Mycoplasma haemofelis, M. haemominutum)5 mg/kgIM, SCevery 14 daysuntil able to maintain a normal PCV๐ŸŒŽ NA
Feline clinical ehrlichiosis or anaplasmosis5 mg/kgIMevery 14 daysfor at least 2-4 treatments๐ŸŒŽ NA
Treatment of large babesial species infection2.5 mg/kgIMonce1 dose๐ŸŒ EU
  • Cytauxzoon felis: Efficacy not proven. Cholinergic effects can be mitigated by pre-treating with atropine. Must also give supportive therapy (IV fluids, prophylactic heparin, nutritional/nursing care, analgesia, and potentially transfusion).
  • Feline hemoplasmosis (Mycoplasma haemofelis, M. haemominutum): Alternative for cats intolerant of doxycycline.
  • Feline clinical ehrlichiosis or anaplasmosis: Alternative to doxycycline.
  • Treatment of large babesial species infection: Dose based on imidocarb dipropionate. Can improve clinical signs. Alternative agents are preferable for smaller species (e.g., B. felis).

Horses

IndicationDoseRouteFrequencyDurationRegion
Equine piroplasmosis (Babesia caballi; Babesia equi)2.2 mg/kgIMonceโ€”๐ŸŒŽ NA
Equine piroplasmosis (Babesia caballi)2 mg/kgIMonce a dayfor 2 days๐ŸŒŽ NA
Equine piroplasmosis (Babesia equi)4 mg/kgIMat 72 hour intervalsfor 4 doses๐ŸŒŽ NA
  • Equine piroplasmosis (Babesia caballi; Babesia equi): Will generally allow clinical signs to subside.
  • Equine piroplasmosis (Babesia caballi): To eliminate B. caballi.
  • Equine piroplasmosis (Babesia equi): B. equi is more difficult to eliminate.

Sheep

IndicationDoseRouteFrequencyDurationRegion
Babesiosis1.2 mg/kgIMrepeat in 10-14 daysโ€”๐ŸŒŽ NA

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

Recording this consult? VetSheet's AI writes the drug, dose and duration straight into a structured visit note.See how VetSheet works

Overview

Imidocarb dipropionate is a diamidine antiprotozoal agent primarily used in veterinary medicine to treat tick-borne protozoal infections.

โ€‹Key Clinical Applications:โ€‹

  • Babesiosis: Highly effective against Babesia canis in dogs, as well as Babesia species in horses and sheep.
  • Cytauxzoonosis: Used in cats for Cytauxzoon felis infections, often as part of a comprehensive treatment protocol.
  • Other Uses: Sometimes utilized as an alternative or adjunct treatment for Ehrlichia canis, Hepatozoon canis, and feline hemotropic mycoplasmas (e.g., Mycoplasma haemofelis).

Clinical Pearl: While highly effective for B. canis, it is generally less effective against B. gibsoni. It does not clear the encysted stage of Hepatozoon americanum.

Mechanism of action

Imidocarb acts by directly targeting the nucleic acids of susceptible protozoal organisms.

  • It binds to and intercalates with DNA โ†’ causing the double helix to unwind and denature.
  • This structural damage โ†’ inhibits cellular repair and replication โ†’ leading to parasite death.
  • Mechanistic Note: As a diamidine derivative, it may also interfere with polyamine synthesis and function, further disrupting the parasite's metabolic pathways.

Safety & warnings

Contraindications

  • Intravenous (IV) administration
  • Patients exposed to cholinesterase-inhibiting drugs
  • Patients exposed to pesticides or certain chemicals

Adverse effects

  • Pain and inflammation at the injection site (rarely ulceration)
  • Salivation (drooling)
  • Nasal drip/discharge
  • Vomiting (usually brief)
  • Panting
  • Diarrhea
  • Restlessness
  • Lacrimation and sweating (horses)
  • Severe renal tubular or hepatic necrosis (rare)
  • Injection site inflammation (mild to severe, potential ulceration)
  • Anaphylactoid reactions (reported in cattle)

Precautions

Important Warnings

  • โ€‹Do NOT administer intravenously (IV).โ€‹
  • Premedication: In cats, puppies, and debilitated dogs, pretreatment with an antimuscarinic agent (e.g., atropine or glycopyrrolate) is strongly advised to mitigate cholinergic side effects.
  • Organ Dysfunction: Use with caution in patients with impaired lung, hepatic, or renal function; weigh risks versus benefits.
  • Species Sensitivities: Donkeys appear to be particularly sensitive to the toxic effects of imidocarb.
  • Reproductive Safety: Safety in puppies, pregnant, lactating, or breeding animals has not been established.

Drug interactions

Cholinesterase-inhibiting drugs (e.g., pyridostigmine)

Increased risk of severe cholinergic toxicity; concurrent use is contraindicated.

Pesticides and chemicals

May exacerbate cholinergic adverse effects and toxicity.

AnticholinesterasesMajor

Increased risk of severe cholinergic toxicity

Monitoring

  • Clinical efficacy (resolution of parasitemia and clinical signs)
  • Adverse effect profile (cholinergic signs, injection site reactions)
  • Creatine kinase (CK) levels (may be significantly increased post-IM injection)
  • Liver and kidney function (especially in cases of suspected overdose or pre-existing disease)
  • Resolution of clinical signs of babesiosis (fever, anemia, lethargy)
  • Blood smears or PCR to confirm parasite clearance
  • Injection site for signs of inflammation, necrosis, or ulceration
  • Immediate post-injection monitoring for cholinergic crisis

Pharmacokinetics

Half-life

CatsUnknownDogsProlonged (exact duration varies)

Absorption

No specific information available in the monograph.

Distribution

No specific information available in the monograph.

Metabolism

No specific information available in the monograph.

Elimination

No specific information available in the monograph.

Overdose

โ€‹Acute Toxicity & Overdose Signs:โ€‹

  • Dogs: At 1.5X the labeled dose (9.9 mg/kg), dogs exhibited signs of liver injury (mildly elevated liver enzymes), pain/swelling at the injection site, and vomiting.
  • General Overdose/Chronic Toxicity: Presents primarily with severe cholinergic signs (vomiting, weakness, lethargy, excessive salivation) or adverse changes in liver, kidney, lung, or intestinal function.
  • Horses: The reported LD-50 is 16 mg/kg.

โ€‹Treatment:โ€‹

  • Atropine or other antimuscarinics may be highly useful to treat the cholinergic signs associated with imidocarb toxicity.
  • Provide symptomatic and supportive care for organ dysfunction.

Available products

Formulations

  • Injection (120 mg/mL)
  • Injectable solution: 85 mg/ml imidocarb base (equivalent to 121.15 mg/ml imidocarb dipropionate)

Veterinary

  • Imidocarb Dipropinate for IM or SC Injection: 120 mg/mL in 10 mL multi-dose vials (Imizolยฎ)
  • Imizol 85 mg/ml solution for injection (121.15 mg/ml imidocarb dipropionate)

Regulatory status

European Unionโœ“ ApprovedPrescription onlyEMA
๐Ÿ„ Cattle

Withdrawal times: cattle meat 213 days ยท cattle milk 21 days

Licensed primarily for cattle; used off-label in dogs and cats under the cascade.

United Kingdomโœ“ ApprovedPrescription only ยท POM-VVMD
๐Ÿ„ Cattle

Withdrawal times: cattle meat 213 days ยท cattle milk 21 days

Licensed primarily for cattle; used off-label in dogs and cats under the cascade.

No regulatory data for: ๐Ÿ‡บ๐Ÿ‡ธ US ยท ๐Ÿ‡ญ๐Ÿ‡ฐ HK ยท ๐Ÿ‡น๐Ÿ‡ผ TW ยท ๐Ÿ‡ฏ๐Ÿ‡ต JP ยท ๐Ÿ‡ฐ๐Ÿ‡ท KR ยท ๐Ÿ‡ฆ๐Ÿ‡บ AU

Storage & stability

Store between 2ยฐ-25ยฐC (36ยฐ-77ยฐF) and protect from light.

Client information

Important: This medication is administered exclusively by your veterinarian via injection.

  • Purpose: Imidocarb is used to treat serious, tick-borne blood parasite infections such as Babesia or Cytauxzoon.
  • What to Expect: The injection can be quite painful. Shortly after receiving the medication, your pet may experience drooling, a runny nose, panting, or brief episodes of vomiting. These are known, common reactions and usually pass quickly.
  • Precautions: Please inform your veterinarian immediately if your pet has recently been exposed to any flea/tick dips, pesticides, or is taking other medications (especially those affecting the nervous system), as these can increase the risk of severe side effects.

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