Negara: Australia
Bahasa: Inggris
Sumber: APVMA (Australian Pesticides and Veterinary Medicines Authority)
CLOPROSTENOL AS THE SODIUM SALT
INTERVET AUSTRALIA PTY LIMITED
cloprostenol as Na salt(250ug/mL)
PARENTERAL LIQUID/SOLUTION/SUSPENSION
CLOPROSTENOL AS THE SODIUM SALT PROSTAGLANDIN Active 250.0 ug/ml
10 x 20mL; 100mL; 20mL
VM - Veterinary Medicine
INTERVET AUSTRALIA
CATTLE | HORSE | BEEF | BOS INDICUS | BOS TAURUS | BOVINE | BUFFALO | BULL | BULLOCK | CALF | COLT | COW | DAIRY COW | DONKEY |
ENDOCRINE SYSTEM
BOVINE OESTRUS CYCLE | EQUINE OESTRUS CYCLE | CTRL OF OESTRUS REL.BEHAVIOUR
Poison schedule: 4; Withholding period: WHP: MEAT: (CATTLE HORSES): DO NOT US E less than one day before slaughter fo r human consumption. MILK: NIL.; Host/pest details: CATTLE: [BOVINE OESTRUS CYCLE]; HORSE: [EQUINE OESTRUS CYCLE]; A luteolytic agent for clinical use and the control of the bovine and equine oestrus cycles.Should not be administered to pregnant animals where the foetus is not to be aborted. Care should be taken when handling this product especially by women of child bearing age and also by asthmatics.
Registered
2023-07-01
ESTRUMATE SYNTHETIC PROSTAGLANDIN FOR CATTLE AND HORSES 36076/107149 Product Name: APVMA Approval No: Label Name: ESTRUMATE SYNTHETIC PROSTAGLANDIN FOR CATTLE AND HORSES Signal Headings: PRESCRIPTION ANIMAL REMEDY KEEP OUT OF REACH OF CHILDREN FOR ANIMAL TREATMENT ONLY Constituent Statements: 250 ug/ml CLOPROSTENOL AS THE SODIUM SALT Claims: A luteolytic agent for clinical use and the control of the bovine and equine oestrous cycles. ESTRUMATE a synthetic prostaglandin analogue for use in cattle and horses, is structurally related to Prostaglandin F2a (PGF2a). Each mL of the colourless aqueous solution contains 263ug of cloprostenol sodium equivalent to 250ug cloprostenol. The solution also contains 2% benzyl alcohol Ph. Eur. as a bactericide. Action: ESTRUMATE is a potent luteolytic agent, i.e. it causes functional and morphological regression of the corpus luteum (luteolysis) in a variety of circumstances. Luteolysis is usually followed by return to oestrus two to four days after treatment, and normal ovulation. Net Contents: 10 x 20mL 100mL 20mL Directions for Use: For use by or under direction of a registered veterinarian DIRECTIONS FOR USE Contraindications: ESTRUMATE should not be administered to pregnant animals where the foetus is not to be aborted, since luteolysis at some stages of gestation will result in the loss of the foetus. ESTRUMATE should not be administered by intravenous injection. Side Effects: Note: There is a refractory period of four to five days after ovulation when cattle are insensitive to the luteolytic effect of prostaglandins. ESTRUMATE has a good safety margin and does not impair fertility. No deleterious effects have been reported on the progeny conceived at the oestrus following treatment. RLP APPROVED In cattle adverse reactions have not been seen at up to 80 times the effective recommended dose (500μg). The only clinically apparent effect was mild and transient diarrhoea. In horses adverse reactions including sweating (occurring within about 20 minutes of treatment), increased Baca dokumen lengkapnya
PRODUCT NAME: ESTRUMATE SYNTHETIC PROSTAGLANDIN FOR CATTLE AND HORSES MATERIAL SAFETY DATA SHEET THIS REVISION ISSUED: AUGUST, 2009 PAGE: 1 OF 6 MATERIAL SAFETY DATA SHEET Issued by: Intervet Australia Pty Limited Phone: 1 800 033 461 (Business Hours) Poisons Information Centre: 13 11 26 from anywhere in Australia, (0800 764 766 in New Zealand) SUBSTANCE: Water solution of Cloprostenol as the sodium salt. TRADE NAME: ESTRUMATE SYNTHETIC PROSTAGLANDIN FOR CATTLE AND HORSES RECOMMENDED USE: A luteolytic agent for clinical use and the control of the bovine and equine oestrus cycles. APVMA NO: 36076 CREATION DATE: August, 2009 THIS VERSION ISSUED: August, 2009 and is valid for 5 years from this date. STATEMENT OF HAZARDOUS NATURE: THIS PRODUCT IS CLASSIFIED AS: Not classified as hazardous according to the criteria of SWA. Not a Dangerous Good according to the Australian Dangerous Goods (ADG) Code. RISK PHRASES: Not Hazardous - No criteria found. SAFETY PHRASES: S36, S24/25. Wear suitable protective clothing. Avoid contact with skin and eyes. SUSDP CLASSIFICATION: S4 ADG CLASSIFICATION: None allocated. Not a Dangerous Good under the ADG Code. UN NUMBER: None allocated PHYSICAL DESCRIPTION & COLOUR: Clear colourless aqueous solution. ODOUR: No data. MAJOR HEALTH HAZARDS: no significant risk factors have been found for this product. This is a physiologically active product and so contact should be minimised, especially if the user is taking a form of medication, as interactions can sometimes give unexpected and undesired results. Contains Cloprostenol Sodium which is a synthetic prostaglandin of the F 2 D type, and is a potent luteolytic agent. ESTRUMATE can be absorbed through the skin and therefore, care should be taken when handling this product, especially by women of child bearing age and also by asthmatics. INHALATION: SHORT TERM EXPOSURE: Available data indicates that this product is not harmful. In addition product is unlikely to cause any discomfort or irritation. LONG TERM EXPOSURE: No data for health effects Baca dokumen lengkapnya