Luteoplan 250 micrograms/ml Solution for Injection for Cattle and Horses
Active ingredient: Cloprostenol
Form
Injection
Species
Manufacturer
Syn Vet-Pharma Ireland Limited
VMD MA No.
54400/5000
What it's used for
Cattle (cows and heifers): - Oestrus induction and synchronisation in cows and heifers with a functional corpus luteum. - Induction of oestrus as an aid to...
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Luteoplan 250 micrograms/ml Solution for Injection for Cattle and Horses — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 26 Mar 2026.
- Oestrus induction and synchronisation in cows and heifers with a functional
corpus luteum.
- Induction of oestrus as an aid to management of suboestrus (‘silent heat’).
- Treatment of clinical and subclinical endometritis in the presence of a
functional corpus luteum.
- Treatment of ovarian luteal cysts.
- Induction of parturition after day 270 of gestation.
- Induction of abortion up today 150 of gestation.
Horses (mares):
- Oestrus induction and synchronisation in mares with a functional corpus
luteum.
- Termination of early pregnancy between day 5 and day 120 of gestation.
Revised: March 2026
AN: 01224/2025
is not intended.
Do not administer to induce parturition in animals with suspected dystocia due
to mechanical obstruction or abnormal position, presentation and/or posture of
the foetus.
Do not use in animals with compromised cardiovascular function,
bronchospasm or gastrointestinal dysmotility.
Do not use in cases of hypersensitivity to the active substance or to any of the
excipients.
Rare
(1 to 10 animals / 10,000
animals treated):
Injection site infection
Very rare
(<1 animal / 10,000 animals
treated, including isolated
reports):
Anaphylaxis
;
Increased respiratory rate
;
Increased heart rate
;
Abdominal pain
, Diarrhoea
3,5
;
Incoordination
;
Lying down
;
Retained placenta
, Metritis
, Dystocia
, Stillbirth
;
Restlessness, Frequent urination
3,5
May occur if anaerobic bacteria enter the injection site, especially following
intramuscular injection, and may become generalized. Aggressive antibiotic
therapy, particularly covering clostridial species, should be employed at the first
sign of infection. Careful aseptic techniques should be employed to decrease
the possibility of these infections.
Requiring immediate medical attention. Can be life-threatening.
Cloprostenol may cause effects similar to Prostaglandin F2α
in the
smooth muscles.
May be caused by induction of parturition or abortion. As part of induction of
parturition, depending on the date of treatment versus the date of conception,
the incidence of placental retention may be increased.
In case of occurrence, these effects are observed within 15 minutes post-
injection and usually disappear after one hour.
Revised: March 2026
AN: 01224/2025
Horses (mares):
Uncommon
(1 to 10 animals / 1,000 animals
treated):
Abnormal oestrus
Rare
(1 to 10 animals/ 10,000
animals treated):
Injection site infection
Very rare
(<1 animal / 10,000 animals
treated, including isolated
reports):
Anaphylaxis
;
Increased respiratory rate
;
Increased heart rate
;
Increased sweating
4,5
;
Abdominal pain
, Colic
, Diarrhoea
4,8
;
Incoordination
, Muscle tremor
;
Lying down
, Decreased body temperature
;
Retained placenta
, Metritis
, Dystocia
, Stillbirth
;
Restlessness, Frequent urination
4,8
Haemorrhagic (anovular) follicles and multiple ovulations are reported in
literature for horses treated with cloprostenol.
May occur if anaerobic bacteria enter the injection site, especially following
intramuscular injection, and may become generalized. Aggressive antibiotic
therapy, particularly covering clostridial species, should be employed at the first
sign of infection. Careful aseptic techniques should be employed to decrease
the possibility of these infections.
Requiring immediate medical attention. Can be life-threatening.
Cloprostenol may cause effects similar to Prostaglandin F2α activity in the
smooth muscles.
Appears to be transient and resolves without any treatment.
Mild.
May be caused by termination of gestation, depending on the date of
treatment versus the date of conception, the incidence of placental retention
may be increased.
In case of occurrence, these effects are observed within 15 minutes post-
injection and usually disappear after one hour.
Reporting adverse events is important. It allows continuous safety monitoring of
a veterinary medicinal product. Reports should be sent, preferably via a
veterinarian, to either the marketing authorisation holder or its local
representative or the national competent authority via the national reporting
system. See the package leaflet for respective contact details.
in cattle and horses), when females are insensitive to the luteolytic effect of
prostaglandins.
For the termination of gestation in cattle, best results are obtained before day
100 of gestation. Results are less reliable between day 100 and 150 of
gestation.
Special precautions for use in animals
To reduce the risk of anaerobic infections arising from vasoconstriction at the
injection site, injections into contaminated (wet or dirty) skin areas should be
avoided. Thoroughly clean and disinfect injection sites prior to administration.
Do not administer intravenously.
All animals should receive adequate supervision after treatment.
Induction of parturition or abortion may cause dystocia, stillbirth and/or metritis.
The incidence of retained placenta may be increased depending on the time of
treatment relative to the date of conception.
Injection into adipose tissue can result in incomplete absorption of the
veterinary medicinal product.
Cloprostenol may cause effects related to Prostaglandin activity in the
smooth muscles, such as increased frequency of urination and defecation.
Special precautions to be taken by the person administering the veterinary
medicinal product to animals
Prostaglandins of the F2α type, such as cloprostenol, may be absorbed through
the skin and may cause bronchospasm or miscarriage. Care should be taken
when handling the veterinary medicinal product to avoid self-injection or skin
contact.
Pregnant women, women of childbearing age, asthmatics and persons with
other respiratory tract diseases should avoid contact when handling this
veterinary medicinal product. Personal protective equipment consisting of
impervious gloves should be worn when handling the veterinary medicinal
Revised: March 2026
AN: 01224/2025
product.
Accidental spillage on the skin should be washed immediately with soap and
water. If accidental contact with eyes occurs, rinse the affected eyes thoroughly
with clean, fresh water. In case of accidental self-injection or spillage onto the
skin seek medical advice immediately, particularly as shortness of breath may
occur, and show the package leaflet or label to the physician.
Chlorocresol may cause irritation and allergic reactions. People with known
hypersensitivity to chlorocresol should administer the veterinary medicinal
product with caution.
Wash hands after use.
Special precautions for the protection of the environment
Not applicable.
uterus.
The concomitant use of progestogens decreases the effect of cloprostenol.
Do not administer with non-steroidal anti-inflammatory drugs (NSAIDs) since
they inhibit endogenous prostaglandin synthesis.
storage conditions.
This veterinary medicinal product should be stored upright.
Revised: March 2026
AN: 01224/2025
Meat and offal: 1 day.
Milk: Zero hours.
Horses:
Meat and offal: 2 days.
Milk: 24 hours.
5.
This information is sourced from the official Summary of Product Characteristics (SPC) published by the Veterinary Medicines Directorate (VMD). It is provided for informational purposes only and does not replace professional veterinary advice. Always consult your vet before administering any medication.
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Other Products Containing Cloprostenol
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
Bioestrovet 0.250 mg/ml Solution for Injection for Cattle
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Cevaprost 250 µg/ml Solution for Injection
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Cyclix 250 microgram/ml Solution for Injection for Cattle
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