Vetivex 6 (Glucose 5% W/V Intravenous Infusion Bp (Vet))
Revised: March 2011
Amended pages
SUMMARY OF PRODUCT CHARACTERISTICS
1. NAME OF THE VETERINARY MEDICINAL PRODUCT
VETIVEX 6 (Glucose 5 % w/v Intravenous Infusion BP (Vet))
2. QUALITATIVE AND QUANTITATIVE COMPOSITION
Glucose monohydrate 5.5 % w/v
(equivalent to anhydrous glucose 5.0 % w/v)
Each one litre provides approximately 200 kcal.
3. PHARMACEUTICAL FORM
A clear, colourless solution for infusion.
4. CLINICAL PARTICULARS
4.1 Target species
Cattle, calves, horses, dogs and cats.
4.2 Indications for use, specifying the target species
This product is administered by intravenous infusion for the treatment of dehydration (in the absence of shock) in cattle, calves, horses, dogs and cats. It is used to replace water when it cannot be taken or retained orally.
Glucose infusions are used to correct hypernatraemia (by replacing lost water) and hyperkalaemia (through the promotion of insulin production which in turn causes potassium to move from plasma into cells). It is not a significant calorie source but can provide transient improvement of hypoglycaemia.
4.3 Contraindications
This product should not be administered to hyperglycaemic animals.
4.4 Special warnings for each target species
None.
4.5 Special precautions for use
i. Special precautions for use in animals
This product should be used with care in diabetic patients.
A risk of thrombosis with intravenous infusion should be considered.
This product should not be administered at rate in excess of 10 ml/kg/hour, otherwise glycosuria and osmotic diuresis may result. Furthermore, severe or long-standing hypernatraemia should be corrected gradually.
ii. Special precautions to be taken by the person administering the medicinal product to animals
No special precautions required.
iii. Other precautions
None required.
4.6 Adverse reactions (frequency and seriousness)
Monitor fluid output and blood glucose.
4.7 Use during pregnancy and lactation or lay
Use under veterinary supervision.
4.8 Interaction with other medicaments and other forms of interaction
Incompatibility with certain antibiotics and heparin are recognised.
4.9 Amounts to be administered and administrationroute
This product should be administered intravenously at a rate not exceeding 10 ml/kg/hour.
Maintain aseptic precautions
4.10 Overdose (symptoms, emergency procedures, antidotes) if necessary
Monitor fluid output and blood glucose.
4.11 Withdrawal periods
Zero days.
5. PHARMACOLOGICAL PROPERTIES
Pharmacotherapeutic group: Blood substitutes and perfusion solutions, I.V. solutions, Solutions for parenteral nutrition
ATC Vet Code: QB05BA03. Solutions affecting the electrolyte balance
5.1 Pharmacodynamic properties
Glucose 5 % w/v Intravenous Infusion BP (Vet) is used as a replacement source of water and glucose for animals who cannot be given rehydration fluids orally. It is temporarily isotonic (thereby avoiding causing osmotic shock to red blood cells), the glucose is then metabolised leaving water. The glucose can provide a transient source of nutrient and will aid in correction of a hyperkalaemia.
5.2 Pharmacokinetic properties
Intravenous infusion ensures rapid distribution. The constituents of the infusion solution will be metabolised and excreted through the same pathways as those substances derived from normal dietary sources.
6. PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Water for injections
6.2 Incompatibilities
None stated.
6.3 Shelf-life
Do not use unless the solution is clear, free from visible particles, and the container is undamaged.
Unopened: 2 years.
After opening: The product does not contain an antimicrobial preservative. It is intended for single use only and any unused contents should be discarded.
6.4 Special precautions for storage
Do not store above 25°C. Do not freeze.
Nature and composition of immediate packaging
Presented in polyvinylchloride (PVC) infusion bags, over-wrapped with polypropylene, in cartons of 20 x 500 ml and 10 x 1000 ml.
Not all pack sizes may be marketed.
Each carton contains sufficient number of package leaflets so that individual units may be supplied.
6.6 Special precautions for the disposal of unused veterinary medicinal product or waste materials derived from the use of such products, if appropriate
Any unused product or waste material should be disposed of in accordance with national requirements.
7. MARKETING AUTHORISATION HOLDER
Dechra Limited
Dechra House
Jamage Industrial Estate
Talke Pits
Stoke-On-Trent
Staffordshire
ST7 1XW
8. MARKETING AUTHORISATION NUMBER
Vm 10434/4057
9. DATE OF RENEWAL OF THE AUTHORISATION
22 April 2008
10. DATE OF REVISION OF THE TEXT
March 2011
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