Downlands Calcium Borogluconate 40% W/V Cm Solution For Injection
Revised: June 2010
ATCVet code amended
SUMMARY OF PRODUCT CHARACTERISTICS
1. Name of the veterinary medicinal product
Downlands Calcium Borogluconate 40% w/v CM Solution for Injection
2. Qualitative and quantitative composition
Active Substance:
Contains Calcium Borogluconate 33.33% w/v and Magnesium Hypophosphite Hexahydrate 5% w/v
Each 400 ml contains:
11.9 g calcium (provided by calcium gluconate and calcium borogluconate) and 1.85 g magnesium hypophosphite hexahydrate)
Also contains 6.84% w/v boric acid.
Excipients:
For a full list of excipients, see section 6.1
3. Pharmaceutical form
Solution for Injection
A clear pale yellow solution
4. Clinical Particulars
4.1 Target species
Cattle
Indications for use, specifying the target species
Downlands Calcium Borogluconate 40% CM is indicated in the treatment of hypocalcaemia in cattle where increased blood magnesium levels are required.
4.3 Contraindications
None
4.4 Special Warnings for each target species
None
4.5 Special precautions for use
i. Special precautions for use in animals
The solution should be warmed to body temperature before administration. Intravenous injections should be given slowly in order to avoid possible neuromuscular dysfunction and cardiac insufficiency. Normal aseptic precautions should be observed. Sites of subcutaneous administration should be messaged gently.
ii. Special precautions to be taken by the person administering the veterinary medicinal product to animals
Care should be taken to avoid accidental self-injection. If accidental self- injection occurs, seek medical advice. Wash hands after use.
4.6 Adverse reactions (frequency and seriousness)
Occasional temporary swelling may occur at sites of subcutaneous administration.
4.7 Use during pregnancy, lactation or lay
Downlands Calcium Borogluconate 40% CM is safe for use during pregnancy and lactation.
4.8 Interaction with other medicinal products and other forms of interaction
None
4.9 Amounts to be administered and administration route
Administer by subcutaneous or slow intravenous injection
Cattle : 200 - 400 ml
Overdose (symptoms, emergency procedures, antidotes), if necessary
Not applicable.
Withdrawal period
Meat – Zero days
Milk – Zero hours
5. pharmacological properties
Pharmacotherapeutic group: Mineral supplements, Calcium, Calcium, combinations with other drugs
ATC Vet Code: QA12AX
5.1 Pharmacodynamic properties
Calcium Borogluconate and Magnesium Hypophosphite are soluble salts of calcium and magnesium respectively used extensively in fluid infusions in correction of metabolic disturbances. On parenteral administration they rapidly increase plasma concentrations of calcium, magnesium and phosphorus. This is effective in the treatment of hypocalcaemia with associated magnesium and phosphorus deficiencies.
6. Pharmaceutical particulars
6.1 List of excipients
Sodium Bicarbonate 10% or Boric Acid 5% (for pH adjustment)
Water for Injections
Incompatibilities
None known
Shelf life
Shelf life of the veterinary medicinal product as packaged for sale:
Glass bottles 2 years.
Polypropylene vials 18 months
Special precautions for storage
Do not store above 25oC. Protect from light.
This product does not contain an antimicrobial preservative. Any solution remaining in the vial following withdrawal of the required dose should be discarded.
Nature and composition of immediate packaging
Downlands Calcium Borogluconate 40% CM is marketed in either 400 ml Amber Type III glass vials sealed using black rubber wads and aluminium screw caps, or 400ml polypropylene containers sealed with bromobutyl bungs and aluminium caps.
Special precautions for the disposal of unused veterinary medicinal product or waste materials derived from the use of such products
Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal products should be disposed of in accordance with local requirements.
7. MARKETING AUTHORISATION HOLDER
Norbrook Laboratories Limited
Station Works
Newry
Co. Down
BT35 6JP
8. MARKETING AUTHORISATION NUMBER(S)
Vm 02000/4214
9. DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
Date of first authorisation: 5th July 1999
10. DATE OF REVISION OF THE TEXT
June 2010
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