Cloprostenol Sodium Injectioninstructions

Common Name

Cloprostenol Sodium Injection

Main Ingredient

Cloprostenol Sodium

Characteristics

This product is a colorless clear liquid.

Pharmacological Action

This product is an artificially synthesized prostaglandin F2α homolog. Has a strong dissolving effect on the corpus luteum, can quickly cause luteal regression, and inhibit its secretion; It also has a direct excitatory effect on uterine smooth muscle, which can cause uterine smooth muscle contraction and cervical relaxation. For animals with normal sexual cycles, estrus usually occurs within 2~5 days after treatment. Pregnant cows between 10~150 days of gestation typically experience miscarriage 2~3 days after injection medication.

Indications

Prostaglandins. It has a powerful luteolysis and direct excitation of uterine smooth muscle, and is mainly used for controlling estrus in cows and inducing parturition in pregnant sows.

Dosage and Administration

Intramuscular injection: one dose, cattle 0.2~0.3 mg; Pigs, 112~113 days of gestation, 0.05~0.1 mg.

Precautions

(1)Prohibited for pregnant animals.

(2)When inducing labor, premature use is strictly prohibited.

(3)This product can induce miscarriage or acute bronchospasm, and should be used with caution. Pregnant women and individuals with asthma and other respiratory diseases should be particularly careful when operating it.

(4)This product is easily absorbed through the skin. Wear rubber or disposable protective gloves during operation. Wash hands thoroughly with soap and water after operation and before drinking or eating. If this product is stuck or spattered on the skin, wash it off immediately with clean water.

(5)This product is easily absorbed through the skin, and rubber or secondary protective gloves should be worn during operation. After operation and before drinking or eating, wash hands thoroughly with soap and water. If the product sticks or splashes on the skin, it should be rinsed off with water immediately.

(6)This product should not be used in conjunction with antipyretic.

(7)After the product is used up, the empty bottle should be buried or incinerated. Waste generated by this product should be handled in the approved waste treatment equipment, it is strictly prohibited to dispose of the undiluted product on site. It is strictly prohibited to dispose of the undiluted product on site. Do not contaminate drinking water, feed and food.

Adverse Reactions

The use of this product in the late pregnancy can increase the risk of dystocia in animals, and the efficacy of the drug decreases.

Withdrawal Period

None

Specification

Calculated as C22 H29ClO6, (1)2 ml:0.1 mg;(2)2 ml:0.2 mg;(3)50 ml:5 mg.

Package

(1)2 ml:0.1 mg, 10 ampoules;(2)2 ml:0.2 mg, 10 ampoules;(3)50 ml:5 mg, 1 bottle.

Storage

Airtight, store in a cool and dark place.

Shelf Life

2 years