Country: United Kingdom
Language: English
Source: VMD (Veterinary Medicines Directorate)
Propylene Glycol
Norbrook Laboratories Limited
QA16QA01
Propylene Glycol
Oral solution
AVM-GSL - Authorised Veterinary Medicine – General Sales List
Cattle, Sheep
Gastrointestinal metabolic
Expired
1986-06-30
Revised: 28 th August 2008 AN: 02089/2007 SUMMARY OF PRODUCT CHARACTERISTICS 1. NAME OF THE VETERINARY MEDICINAL PRODUCT Ketosaid 99.96% w/w Oral Solution 2. QUALITATIVE AND QUANTITATIVE COMPOSITION ACTIVE SUBSTANCE: Each ml contains 0.9996 ml of active substance Qualitative composition Quantitative composition Propylene glycol 99.96% w/w EXCIPIENTS: Carmoisine 0.04% w/w For a full list of excipients, see section 6.1 3. PHARMACEUTICAL FORM Oral solution A red, viscous, non-aqueous solution 4. CLINICAL PARTICULARS 4.1 TARGET SPECIES Cattle Sheep 4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES Ketosaid is used as an aid in the treatment of acetonaemia and ketosis in cattle and sheep. 4.3 CONTRAINDICATIONS For oral administration only. 4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES None 4.5 SPECIAL PRECAUTIONS FOR USE SPECIAL PRECAUTIONS FOR USE IN ANIMALS Revised: 28 th August 2008 AN: 02089/2007 As Ketosis in sheep arises from prenatal metabolic stress, treatment with Ketosaid may be continued until symptoms resolve or until parturition. During this time a general improvement in nutritional status is recommended. SPECIAL PRECAUTIONS TO BE TAKEN BY THE PERSON ADMINISTERING THE VETERINARY MEDICINAL PRODUCT TO ANIMALS In case of accidental eye contact, wash eyes with plenty of clean water. If irritation occurs, seek medical attention. In case of contact with skin, remove any contaminated clothing and wash affected area thoroughly with soap and water. If irritation occurs seek medical advice. Ingestion: If accidentally swallowed, seek medical advice. Wash hands after use. 4.6 ADVERSE REACTIONS (FREQUENCY AND SERIOUSNESS) No known undesirable effects. 4.7 USE DURING PREGNANCY, LACTATION OR LAY Ketosaid can be safely administered to pregnant and lactating animals. 4.8 INTERACTION WITH OTHER MEDICINAL PRODUCTS AND OTHER FORMS OF INTERACTION None 4.9 AMOUNTS TO BE ADMINISTERED AND ADMINISTRATION ROUTE Cattle: 200 ml twice daily on first day and 100 ml twice daily for next three days, administered orally as a drench. Read the complete document