estroPLAN Injection (Canada)This page contains information on estroPLAN Injection for veterinary use.
The information provided typically includes the following:
- estroPLAN Injection Indications
- Warnings and cautions for estroPLAN Injection
- Direction and dosage information for estroPLAN Injection
estroPLAN InjectionThis treatment applies to the following species:
For Veterinary Use Only
cloprostenol 250 µg/mL (as cloprostenol sodium)
An analogue of prostaglandin F2α for intramuscular injection in cattle.
Each mL of estroPLAN contains 263 µg of cloprostenol sodium, equivalent to 250 µg of cloprostenol, in an isotonic citric acid buffer containing the antimicrobial preservative chlorocresol 0.1% w/v.
estroPLAN causes rapid regression of the functional corpus luteum in cattle. In non-pregnant cycling cattle luteolysis is usually followed by ovarian follicular development and a return to estrus with normal ovulation in 2 - 5 days after treatment. The early corpus luteum is insensitive to the effects of prostaglandin (PG); in cattle this refractory period spans the first 4 - 5 days before and after ovulation. In animals with prolonged luteal function (pyometra, mummified fetus) the induced luteolysis usually results in resolution of the condition and return to cyclicity. Pregnant animals may abort depending on the stage of gestation.
estroPLAN Injection Indications
For intramuscular use to induce luteolysis in cattle. The luteolytic action of estroPLAN can be utilized to manipulate the estrus cycle to better fit certain management practices, to terminate pregnancies resulting from mismating and to treat certain conditions associated with prolonged luteal function.
estroPLAN can be used in the following clinical situations:
Unobserved Or Non-detected Estrus (in Cows With Normal Corpora Lutea)
Cows may be cycling but either fail to display behavioral estrus or display only very subtle signs. This condition occurs most commonly in high yielding dairy cows at peak lactation. The presence of ovarian cyclical activity should be determined by rectal palpation of a normal corpus luteum prior to estroPLAN administration. Estrus should commence 2 - 5 days following treatment. Failure of estrus induction may result if the treatment is given during the refractory period of the corpus luteum. Treated animals should be inseminated at the usual time following detection of estrus or, if estrus detection is not practiced, inseminated twice at 72 and 96 hours post injection.
Pyometra Or Chronic Endometritis
Damage to the reproductive tract at calving or post partum retention of the placenta often leads to infection and inflammation of the uterus (endometritis). Under certain circumstances, this may progress into chronic endometritis with the uterus becoming distended with purulent matter. This condition, commonly referred to as pyometra, is characterized by a lack of cyclical estrus behavior and the presence of a persistent corpus luteum. Induction of luteolysis with estroPLAN usually results in evacuation of the uterus and a return to normal cyclical activity. Where necessary, treatment may be repeated after 10 - 14 days.
Termination Of Pregnancies From Mismating, Abortion In Feedlot Heifers
Unwanted pregnancy can be terminated by treatment with estroPLAN from about one week after mating until about 4 1/2 months of gestation. The induced abortion is normally uncomplicated and the fetus and placenta are usually expelled about 4 - 5 days after injection with the reproductive tract returning to normal soon after the abortion. Treated animals should be closely observed until expulsion of the fetus and placental membranes is complete. The ability of estroPLAN to induce abortion decreases beyond 4 1/2 months of gestation while the risk of dystocia and its complications increases.
Termination Of Abnormal Pregnancy: Mummified Fetus
Fetal death may result in the mummification of the fetus in utero. Treatment with estroPLAN at any stage of gestation will usually result in luteolysis and expulsion of the mummified fetus from the uterus. Occasionally manual removal of the fetus from the vagina is necessary. Normal cyclical activity usually follows.
estroPLAN can be used in a number of treatment regimens to synchronize the estrus cycle and ovulation of groups of cows. Cloprostenol induces luteolysis of functional corpora lutea, with estrus occurring in most cows in 2 - 5 days. However, it should be noted that the corpus luteum is refractory to the effects of PG in the first 4 - 5 days before and after ovulation.
estroPLAN can be incorporated into a controlled breeding program as follows:
1. single Estroplan Injection
Only animals with a mature corpus luteum should be treated. The presence of an anatomically normal, nonpregnant reproductive tract, ovarian cyclical activity and the presence of a mature corpus luteum should be determined by rectal palpation prior to estroPLAN administration. If these criteria are met, estrus is expected to occur 2 - 5 days following injection, at which time animals may be inseminated. Treated animals should be inseminated at the usual time following detection of estrus or, if estrus detection is not practiced, inseminated twice at 72 and 96 hours post injection.
With a single injection program it may be desirable to assess the cyclicity status of the herd before estroPLAN treatment. This can be accomplished by heat detecting and breeding at the usual time following detection of estrus for a six day period, all prior to injection. If by the sixth day the cyclicity status appears normal (approximately 25 - 30% detected in estrus) all cattle not already inseminated should be palpated for normality, non-pregnancy, and cyclicity, then injected with estroPLAN.
2. double Estroplan Injections
The presence of an anatomically normal, non-pregnant reproductive tract and ovarian cyclical activity should be determined by rectal palpation prior to administration of the first estroPLAN injection. A second injection of estroPLAN should be given 11 days following the first injection. In normal cycling animals estrus is expected to occur 2 - 5 days following the second injection. Treated animals should be inseminated at the usual time following detection of estrus or, if estrus detection is not practiced, inseminated twice at 72 and 96 hours post injection.
Many animals will come into estrus following the first injection. Those animals can be inseminated at the usual time following detected estrus. Animals not inseminated should receive a second injection 11 days after the first injection.
Any controlled breeding program recommended should be completed by either:
- Observing animals (especially during the third week after injection) and inseminating or hand mating any animals returning to estrus,
- Turning in clean-up bull(s) 7 - 8 days after the last injection of estroPLAN to cover any animals returning to estrus
Requirements For Controlled Breeding Programs
A variety of programs can be designed to best meet the needs of individual management systems. A controlled breeding program should be selected which is appropriate for the existing circumstances and management practices.
Before a controlled breeding program is planned the producer’s objectives must be examined and he must be made aware of the projected results and limitations. The producer and his consulting veterinarian should review the operation’s breeding history, herd health and nutritional status and agree that a controlled breeding program is practical in the producer’s specific situation.
To achieve good results with planned mating programs, several key factors must be given adequate consideration:
- A high proportion of cows in the herd need to be cycling normally, as PGs are only effective in cows with mature corpora lutea. This may not be the case in herds in which there are many first calvers, late calvers or cows in poor condition.
- Cows must be in a fit and healthy breeding condition and on an adequate or increasing plane of nutrition. Animals in poor or medium condition should be fed to ensure a positive nutritional balance for 4 - 6 weeks before estroPLAN treatment and for 4 weeks after treatment.
- Proper program planning and record keeping are essential.
- Estrus detection needs to be of a high standard.
- If artificial insemination is being used, a competent technician using high quality semen must perform insemination.
Provision must be made to supervise the calving of a large number of cattle over a short period of time.
estroPLAN Injection Dosage And Administration
Only cattle with a functional CL can respond to the luteolytic action of estroPLAN. In the cycling animal there are refractory periods of 4 to 5 days before and after ovulation when cattle are not responsive to PGs.
For therapeutic indications and controlled breeding: 2 mL estroPLAN injection by intramuscular injection.
For abortion: 1.5 mL (2 mL for animals over 455 kg) by intramuscular injection.
Do not administer estroPLAN to pregnant animals whose calf is not to be aborted.
Adverse reactions have not been seen at the recommended dose of cloprostenol 500 µg. At 50 and 100 times the recommended dose of cloprostenol mild side effects may be detected in some cattle, including uneasiness, mild transient diarrhea, slight salivation, and milk letdown.
Treated animals must not be slaughtered for human consumption for at least twenty-four (24) hours after the latest treatment with this drug.
estroPLAN is readily absorbed through skin and may cause abortion and/or bronchospasms. Direct contact with skin should be avoided. Accidental spillage on the skin should be washed off immediately using soap and water. Women of child-bearing age, asthmatics and persons with bronchial and other respiratory problems should exercise extreme caution when handling this product.
Should respiratory distress result from accidental inhalation or injection, the inhalation of a rapidly acting bronchodilator is indicated.
Keep out of reach of children.
estroPLAN Injection Caution
As with all parenteral products, careful aseptic techniques should be employed to decrease the possibility of post injection bacterial infection. A low incidence of clostridial and other infections at the injection site has been reported following PG administration. Treated animals should be closely observed following injection and appropriate antibiotic therapy should be employed at the first sign of infection.
Store below 25°C.
Protect from light: store in product carton.
20 mL multidose vials
100 mL multidose vials
Distributed in Canada by: Vétoquinol N.-A. Inc., 2000, ch. Georges, Lavaltrie, QC J5T 3S5
Manufactured for: Parnell Technologies Pty Ltd, 4/476 Gardeners Road, Alexandria NSW 2015 Australia
Owner of the trademark estroPLAN
NAC No.: 12343172
2000, CHEMIN GEORGES, LAVALTRIE, QC, J5T 3S5
|Every effort has been made to ensure the accuracy of the estroPLAN Injection information published above. However, it remains the responsibility of the readers to familiarize themselves with the product information contained on the Canadian product label or package insert.|
Copyright © 2013 North American Compendiums. Updated: 2013-09-18