GESTAVET PROST
D-CLOPROSTENOL
What it does
D-cloprostenol is a medicine used to help with certain reproductive conditions in animals. It is not commonly used in humans.
Commonly used for: induction of labor in pregnant women, treatment of certain reproductive disorders
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Source: Pharmacy and Poisons Board · fetched 2026-01-28 20:39:31 · updated 2026-08-09 02:03:50
About this medicine
D-cloprostenol is a medicine used to help with certain reproductive conditions in animals. It is not commonly used in humans.
What it treats
- induction of labor in pregnant women
- treatment of certain reproductive disorders
How it works
D-cloprostenol works by mimicking a natural hormone that helps in the process of labor and reproductive functions.
Who it's for
D-cloprostenol is primarily used in veterinary medicine and is not typically prescribed for humans.
AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.
Clinical monograph: dcloprostenol
BNF-referencedDcloprostenol is a synthetic prostaglandin analogue, primarily used for its oxytocic properties in veterinary medicine, specifically in cattle. It is known to induce luteolysis, leading to the termination of pregnancy or synchronization of estrus. Dcloprostenol mimics the action of naturally occurring prostaglandins, which are lipid compounds that have diverse hormone-like effects in various physiological processes.
Indications
- Induction of labor
- Termination of pregnancy
- Estrus synchronization
- Treatment of certain reproductive disorders in cattle
Dosage
Children: Paediatric dosing information is not available. Refer to the BNF for Children for any age-specific dosing recommendations.
Adults: Dosage may vary based on specific conditions and veterinary guidelines. Refer to the BNF for detailed dosing information.
Mechanism of action
Dcloprostenol acts as a potent agonist of the prostaglandin F2α receptor (FP), leading to various biological effects such as smooth muscle contraction, modulation of reproductive cycles, and stimulation of uterine contractions. Its action promotes luteolysis, resulting in decreased progesterone levels, thereby facilitating estrous synchronization and abortion in certain species.
Pharmacodynamics
Dcloprostenol exhibits its effects through the activation of the FP receptor, which is coupled to G-proteins. This leads to an increase in intracellular calcium levels and subsequent contraction of smooth muscle tissues, including the uterus. The drug's effects on the reproductive tract make it valuable in managing reproductive cycles and conditions associated with the estrous cycle in livestock.
Pharmacokinetics
After administration, dcloprostenol is rapidly absorbed and undergoes significant first-pass metabolism. Its bioavailability may vary based on the route of administration. The drug is primarily metabolized by the liver, with metabolites excreted in urine. The elimination half-life may vary, but it is generally short, requiring multiple doses for sustained effects.
Pregnancy
There are no adequate and well-controlled studies in pregnant women. Dcloprostenol should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.
Breast-feeding
Dcloprostenol is excreted in human breast milk. Caution should be exercised when administering to a nursing mother.
Storage
Store at room temperature, protected from light.
Formulations
- {'name': 'Dcloprostenol injection', 'strength': '5 mg/mL', 'form': 'solution for injection'}
AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.
Molecular reference: d-cloprostenol
PubChem CID 5311053Molecular formula: C22H29ClO6
Source: PubChem (NCBI) · pathways from PathBank, Reactome, WikiPathways & PharmGKB.