BVP Copper Injection 100ml
BVP Copper Injection 100ml is a topical injection for animal treatment.
Specially designed for treating animals with copper deficiency.
The use of BVP Copper Injection 100ml can result in toxic reactions or allergic type responses with respiratory distress.
It should be noted that sheep are particularly sensitive to copper toxicity and should only receive BVP Copper Injection 100ml in consultation with your vet.
As copper status on farms can change yearly it is advisable that samples of serum are checked yearly to see if the deficiency still exists before administering BVP Copper Injection 100ml.
Any animal showing a reaction to BVP Copper Injection 100ml should be treated by a Vet ASAP.
Active ingredient:
Copper Methionate for the prevention of copper deficiencies.
Target Species:
Cattle and Sheep
Administration Method
Deep intramuscular injection only into the neck area, using an aseptic technique.
Treatment & control :
Specially designed for treating animals with copper deficiency.
Dosage Rate:
Cattle (adult) 4 – 6 ml.
Ewes 2 ml.
Calves 1 – 2 ml.
Lambs 0.5 ml.
Maximum dose any animal: 6 ml
In Cattle a small nodule can occur at the injection site but this should disappear in less than one month. The likelihood of this happening will be reduced by use of properly injecting the animal. This can be done by avoiding injecting on wet days to reduce the risk of contamination. Be very careful not to overdose, as there is no specific treatment for this. Be very careful of injecting newly purchased animals if you do not know their previous treatment history!
BVP Copper Injection 100ml is best given as an intramuscular injection into the neck muscle. Do not administer intravenously; this method is Vet only and only in very serious circumstances. If after 30 to 40 minutes there is no change in the animal contact your vet ASAP. The dosage of BVP Copper Injection 100ml will depend upon the clinical condition and copper status of the animal. This should be as assessed through serum levels before and after treatment by your vet.
Loss of pigment from coloured hair especially around the eyes, giving the animal a bespectacled appearance (not visible in cattle with white hair around the eyes)
Falling disease – sudden heart failure causing sudden death
Lameness.
Swayback or enzootic ataxia of lambs.
Lambs with this condition cannot coordinate their legs.
They may be severely affected at birth and may be unable to stand; some may be born dead.
Other lambs appear normal at birth but between one and six months they develop an uncoordinated gait.
This condition is caused by impaired development of the central nervous system in the foetus and cannot be reversed by copper treatment once signs appear loss of pigmentation in black sheep.
Because there is usually a wide variation in susceptibility to copper deficiency between individuals within any flock, normal pigmentation in one or two black sheep does not guarantee copper sufficiency among the white-woolled individuals.
Increased incidence in fractures of the long bones and rib bones in lambs.
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Summary of Product Characteristics
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Copper 20mg/ml Suspension for Injection
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each ml contains:
Active substance:
Copper (as copper methionate) 20 mg
Excipient:
Chlorocresol (as preservative) 1 mg
For a full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
A sterile blue suspension for injection.
4 CLINICAL PARTICULARS
4.1 Target Species
Cattle and Sheep.
4.2 Indications for use, specifying the target species
For the prevention and treatment of copper deficiency in cattle and sheep.
4.3 Contraindications
Do not use in animals with known hypersensitivity to the active ingredient.
Not for intravenous administration.
4.4 Special warnings for each target species
The copper status of animals should be checked pre-treatment.
This is particularly important in sheep where overdose can lead to haemolytic crisis.
4.5 Special precautions for use
Special precautions for use in animals
Shake the vial vigorously to re-suspend the solid prior to use.
Inject into a clean site only in the neck area by deep intramuscular injection.
Avoid injection into the rump muscles.
It is generally advised to avoid injection on wet days as this can increase the likelihood of contamination.
The product should not be administered with any other injections.
Special precautions to be taken by the person administering the product to animals
To the user:
Accidental injection/self injection may result in severe pain and swelling, particularly if injected into a joint or finger.
If you are accidentally injected with this product, seek prompt medical advice even if only a very small amount is injected and take the package leaflet with you.
If pain persists for more than 12 hours after medical examination, seek medical advice again.
To the physician:
Even if small amounts have been injected, accidental injection with this product can cause intense swelling, which may, for example, result in ischaemic necrosis.
Expert, PROMPT, surgical attention may be required and may necessitate early incision and irrigation of the injected area, especially where there is involvement of finger pulp or tendon.
4.6 Adverse reactions (frequency and seriousness)
Local tissue reaction may occur at the site of injection in cattle, but will be transient and disappear in less than one month. The use of parenteral injections can sometimes give rise to toxic reactions as well as allergic type responses with respiratory distress. Such reactions should be treated symptomatically.
4.7 Use during pregnancy, lactation or lay
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
Administration is by deep intramuscular injection only into the neck area.
The stopper may be safely punctured up to 10 times.
When treating groups of animals in one run, use a draw-off needle that has been placed in the vial stopper to avoid excess broaching of the stopper.
The draw-off needle should be removed after treatment.
Recommended dosage rate is 20mg copper per 50kg bodyweight in both sheep and cattle.
The dosage and frequency of therapy required depends upon the clinical condition and copper status of the animal as assessed by blood and liver levels both before and after therapy.
The following is given as a guide to dosage:
Lambs: 0.5 ml
Sheep: 2 ml
Calves: 1-2 ml
Adult Cattle: 4-6 ml
4.10 Overdose (symptoms, emergency procedures, antidotes), if necessary
Do not overdose.
There is no specific antidote.
4.11 Withdrawal Period(s)
Milk: Nil.
Meat: Animals intended for human consumption must not be slaughtered until 21 days after the last treatment.
5 PHARMACOLOGICAL or IMMUNOLOGICAL PROPERTIES
The product is designed for prevention and treatment of copper deficiency and clinical conditions associated with copper deficiency. To maintain normal copper levels in lactating dairy cattle.
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Polysorbate 80
Chlorocresol Water for Injections
6.2 Incompatibilities
None known.
6.3 Shelf-life
Shelf life of the veterinary medicinal product as packaged for sale: 3 years.
Any product remaining 28 days after first opening should be discarded.
6.4 Special precautions for storage
Do not store above 25oC.
Protect from light.
6.5 Nature and composition of immediate packaging
A 100 ml clear glass (Type II Ph Eur) multidose injection vial, with chlorobutyl bung and aluminium seal.
6.6 Special precautions for the disposal of unused veterinary medicinal products or waste materials
Any unused product or waste materials should be disposed of in accordance with national requirements.
7 MARKETING AUTHORISATION HOLDER
Tairgi Tread-Lia Baile na Sceilge Teo
(Ballinskelligs Veterinary Products)
Ballinskelligs
Co. Kerry
8 MARKETING AUTHORISATION NUMBER(S)
VPA 10956/005/002
9 DATE OF THE FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
Date of first authorisation: 1st October 1991
Date of first renewal: 29th September 2006
10 DATE OF REVISION OF THE TEXT
November 2015
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