Country: United Kingdom
Language: English
Source: VMD (Veterinary Medicines Directorate)
Glucose Anhydrous
Dechra Limited
QB05BA03
Glucose Anhydrous
Solution for injection
POM-VPS -Prescription Only Medicine – Veterinarian, Pharmacist, Suitably Qualified Person
Cattle, Sheep
Replacement Agent
Authorized
1994-04-20
Revised: September 2016 AN: 00798/2016 Page 1 of 4 SUMMARY OF PRODUCT CHARACTERISTICS 1. NAME OF THE VETERINARY MEDICINAL PRODUCT Glucose 40% w/v Solution for Injection 2. QUALITATIVE AND QUANTITATIVE COMPOSITION ACTIVE SUBSTANCE Qualitative composition Glucose (anhydrous) EXCIPIENTS For a full list of excipients, see section 6.1. Quantitative composition 40.00 % w/v 3. PHARMACEUTICAL FORM Solution for injection. A clear, sterile, aqueous solution. 4. CLINICAL PARTICULARS 4.1 TARGET SPECIES Cattle and sheep. 4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES For the treatment of primary and secondary hypoglycaemia, acetonaemia and as a source of energy in cattle. As an aid in the treatment of pregnancy toxaemia in sheep. 4.3 CONTRAINDICATIONS Do not give by subcutaneous injection. 4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES Intravenous injection should be given slowly, preferably not exceeding 0.5 ml/kg/hour. Do not administer by the subcutaneous route. When acidosis is severe, and renal failure present, treatment is unlikely to be efficacious. 4.5 SPECIAL PRECAUTIONS FOR USE i. Special precautions for use in animals This product does not contain an antimicrobial preservative. Any solution Revised: September 2016 AN: 00798/2016 Page 2 of 4 remaining in the vial following withdrawal of the required dose should be discarded. ii. Special precautions for the person administering the veterinary medicinal product to animals Care should be taken to avoid accidental self-injection. Wash hands after use. 4.6 ADVERSE REACTIONS (FREQUENCY AND SERIOUSNESS) Rapid intravenous injection of dextrose will cause the renal threshold for glucose to be exceeded, with consequent clinical signs of stress and loss of glucose in the urine. For best results intravenous infusions should be given slowly, preferably at a rate not exceeding 0.5 ml/kg/hour. 4.7 USE DURING PREGNANCY, LACTATION OR LAY Not contraindicated. 4.8 INTERACTION WITH OTHER MEDICINAL PRODUCTS AND OTHER FORMS OF INTERACTION None known (supplementary treatment can be Read the complete document