VetSheet

Cloprostenol Sodium

Cloprostenol sodium

Prostaglandin (F-Class Analogue)IMSCDogsHorsesCattleSwineGoats

Also known as: Estrumate Β· estroPLAN Β· ICI-80996

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

1-5 micrograms/kg (0.001-0.005 mg/kg)Not specifiedΒ· once per dayΒ· Up to 2-3 weeks
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
Adjunctive treatment of open cervix pyometra1-5 micrograms/kg (0.001-0.005 mg/kg)Not specifiedonce per dayUp to 2-3 weeks🌎 NA
Adjunctive treatment of open cervix pyometra1 microgram/kgSCevery 5 daysfor 15 days (if not cured earlier)🌎 NA
Pregnancy termination1-2.5 micrograms/kgSConce dailyfor 4-7 days🌎 NA
Pregnancy termination1-2.5 micrograms/kgSCevery 48 hoursfor three doses🌎 NA
  • Adjunctive treatment of open cervix pyometra: When starting treatment, start with one-half the normal dosage and gradually achieve the full dose within 2-3 days.
  • Adjunctive treatment of open cervix pyometra: Give not during feeding. Use with aglepristone at 10 mg/kg SC every 5 days until cured. Give Clavamox (12.5 mg/kg PO twice daily) and supportive hydration throughout protocol.
  • Pregnancy termination: Successful in terminating pregnancy in dogs after 30 days gestation.
  • Pregnancy termination: At higher dose (2.5 mg/kg); appears very effective starting at 30 days of pregnancy. Anticholinergic drug administration (e.g., atropine) 15 minutes prior to dosing appears to lessen adverse effects.

Horses

IndicationDoseRouteFrequencyDurationRegion
To cause abortion prior to the twelfth day of gestation100 microgramsIMonceβ€”πŸŒŽ NA
For luteolysis and to stimulate uterine contractions250 micrograms (total dose)IMonceβ€”πŸŒŽ NA
For luteolysis25-250 micrograms (0.1-1 mL)IMonceβ€”πŸŒŽ NA
As an ecbolic250 micrograms (1 mL)IMq24hβ€”πŸŒŽ NA
  • To cause abortion prior to the twelfth day of gestation: Most effective day 7 or 8 post estrus. Mare will usually return to estrus within 5 days.
  • For luteolysis and to stimulate uterine contractions: Research has shown that 1/10th of a dose can still cause luteolysis and if given on once or on two consecutive days can avoid side effects.
  • For luteolysis: Should not be used more than one day after ovulation because it can damage the corpus luteum and reduce progesterone.

Cattle

IndicationDoseRouteFrequencyDurationRegion
For treatment of pyometra500 microgramsIMonceβ€”πŸŒŽ NA
For pyometra or chronic endometritis, mummified fetus, luteal cysts500 microgramsIMonceβ€”πŸŒŽ NA
For unobserved or undetected estrus in cows with continued ovarian cyclicity and a mature corpus luteum500 microgramsIMonceβ€”πŸŒŽ NA
For abortion, from one week after mating to approximately the 150th day of gestation500 microgramsIMonceβ€”πŸŒŽ NA
For controlled breeding (Single injection method)500 microgramsIMonceβ€”πŸŒŽ NA
For controlled breeding (Double injection method)500 microgramsIMRepeat dose 11 days laterβ€”πŸŒŽ NA
  • For treatment of pyometra: Up to 97% efficacy.
  • For pyometra or chronic endometritis, mummified fetus, luteal cysts: Manual assistance may be required to remove mummified fetus from vagina.
  • For unobserved or undetected estrus in cows with continued ovarian cyclicity and a mature corpus luteum: Estrus should commence in 2-5 days at which time the animal may be inseminated. If estrus detection is not possible, inseminate twice at 72 and 96 hours post injection.
  • For abortion, from one week after mating to approximately the 150th day of gestation: Abortion generally takes place in 4-5 days after injection.
  • For controlled breeding (Single injection method): Use only animals with mature corpus luteum. Inseminate at usual time after detecting estrus, or once at 72 hours, or twice at 72 and 96 hours post injection.
  • For controlled breeding (Double injection method): Estrus should occur in 2-5 days after second injection.

Swine

IndicationDoseRouteFrequencyDurationRegion
To induce parturition in sows175 microgramsIMonceβ€”πŸŒŽ NA
  • To induce parturition in sows: Give 2 days or less before anticipated date of farrowing. Farrowing generally occurs in approximately 36 hours after injection.

Goats

IndicationDoseRouteFrequencyDurationRegion
To induce parturition in does62.5-125 microgramsIMonceβ€”πŸŒŽ NA
To treat pseudopregnancy (hydrometra/mucometra)125 microgramsIMonceβ€”πŸŒŽ NA
  • To induce parturition in does: Give at 144 days of gestation in early morning. Deliveries will peak at 30-35 hours after injection. Maintain goat in usual surroundings and minimize outside disturbances.

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

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Overview

Cloprostenol sodium is a synthetic prostaglandin F2Ξ± (PGF2Ξ±) analogue widely used in veterinary medicine primarily for its potent luteolytic properties. It is structurally related to naturally occurring dinoprost but is significantly more potent and has a longer duration of action.

  • ​Large Animals:​ It is a staple in bovine, equine, and swine reproduction for estrus synchronization, inducing parturition, and managing reproductive pathologies such as luteal cysts, mummified fetuses, or chronic endometritis.
  • ​Small Animals:​ In dogs, it is used off-label for pregnancy termination and the medical management of open-cervix pyometra.

​Clinical Pearl:​ Because it is a synthetic analogue, cloprostenol often exhibits fewer systemic side effects in horses compared to natural PGF2Ξ± (dinoprost), though dogs may still experience significant cholinergic-like adverse effects (which can be mitigated by pre-treatment with anticholinergics like atropine).

Mechanism of action

Cloprostenol acts as a potent agonist at prostaglandin F (FP) receptors.

  • ​Luteolysis:​ Binds to FP receptors on the ​corpus luteum (CL)​ β†’ induces rapid functional and structural regression (luteolysis) β†’ sharp decline in progesterone production. This drop in progesterone removes the negative feedback on the hypothalamus/pituitary, allowing a return to estrus, or induces abortion/parturition depending on the stage of gestation.
  • ​Myometrial Contraction:​ Directly stimulates FP receptors on uterine smooth muscle β†’ increases intracellular calcium β†’ powerful, rhythmic uterine contractions (ecbolic effect).
  • ​Cervical Relaxation:​ Concurrently promotes relaxation and dilation of the cervix, facilitating the expulsion of uterine contents (e.g., fetus, purulent material in pyometra).

Safety & warnings

Contraindications

  • Pregnancy (when abortion or induced parturition are not desired)
  • Intravenous (IV) administration

Adverse effects

  • Increased salivation (dogs)
  • Tachycardia (dogs)
  • Increased urination and defecation (dogs)
  • Gagging and vomiting (dogs)
  • Ataxia and mild depression (dogs)
  • Sweating (horses)
  • Cramping and loose stools (horses)
  • Increased risk of dystocia if used after 5th month of gestation (cattle)

Precautions

Women of child-bearing age, pregnant women, and persons with asthma or other respiratory diseases should use extreme caution when handling cloprostenol, as the drug may induce abortion or acute bronchoconstriction. Cloprostenol is readily absorbed through the skin and must be washed off immediately with soap and water. ​Do not administer IV.​

Drug interactions

Oxytocic agents

Activity may be enhanced by cloprostenol

Monitoring

  • Resolution of clinical signs (e.g., clearance of pyometra)
  • Estrus behavior and timing
  • Confirmation of pregnancy termination/abortion
  • Adverse cholinergic effects in dogs (salivation, vomiting, heart rate)

Pharmacokinetics

Absorption

Readily absorbed through the skin.

Overdose

In cattle, doses of 50 and 100 times those recommended may cause signs of uneasiness, slight frothing, and milk let-down.

In small animals, overdoses of cloprostenol or other synthetic prostaglandin F2Ξ± analogs reportedly can result in severe shock and death.

Available products

Formulations

  • Injection (250 micrograms/mL)

Veterinary

  • Cloprostenol Sodium Injection equivalent to 250 micrograms/mL cloprostenol in 20 mL vials (Estrumate, estroPLAN)

Human-labeled

  • None

Regulatory status

No regulatory data for: πŸ‡ΊπŸ‡Έ US Β· πŸ‡ͺπŸ‡Ί EU Β· πŸ‡¬πŸ‡§ UK 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 at room temperature (15-30Β°C); protect from light.

Client information

​CRITICAL HUMAN SAFETY WARNING:​ Cloprostenol is readily absorbed through the skin and can cause severe adverse effects in humans.

  • Pregnant women, women of child-bearing age, asthmatics, and individuals with bronchial diseases must use extreme caution or avoid handling this product entirely. Accidental exposure can induce abortion or acute bronchospasm (asthma attack).
  • If accidental skin exposure occurs, wash the area immediately with soap and water.
  • This medication should only be handled and administered by individuals fully familiar with its use and safety precautions.
  • In dogs, you may notice side effects like drooling, vomiting, increased urination/defecation, or panting shortly after administration. Your veterinarian may prescribe an additional medication to help minimize these effects.

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.