Animec Super 10mg/ml/100mg/ml Solution for Injection for Cattle.
For the treatment of mixed infestations of adult liver fluke and gastro-intestinal roundworms, lungworms, eye worms, and/or mites and lice of beef and non lactating dairy cattle.
Animec Super Injection is a broad-spectrum endo- and ecto-parasiticide. One dose is effective against many parasites. It is convenient to use.
Animec Super Injection treats:
When cattle have to graze on pasture contaminated with infective larvae of cattle nematodes, Animec Super Injection given at the recommended dosage of 1ml per 50kg bodyweight controls re-infection with the following nematodes up to the duration shown:
Over 300kg give 1ml per 50kg bodyweight.
To ensure a correct dosage, bodyweight should be determined as accurately as possible; accuracy of the dosing device should be checked. If animals are to be treated collectively rather than individually, to avoid under- or over-dosing, they should be grouped according to their bodyweight and dosed accordingly. Inject only by the subcutaneous route.
Divide doses in excess of 10ml between different injection sites.
The timing of treatment should be based on epidemiological factors and should be customised for each individual farm. A dosing program should be established by a qualified professional person.
A sterile 17 gauge ½ inch (15-20 mm) needle is recommended.
Different injection sites should be used for other parenteral products administered concurrently. When using the 500 ml pack size use only automatic syringe equipment. For the 50 ml pack size, use of a multidose syringe is recommended.
The product should be administered under the loose skin in front of or behind the shoulder.
Contra-indications, warnings, etc
Do not use this product intravenously or intramuscularly.
Animec Super Injection is a low volume product authorised for use in cattle. It must not be used in other species as severe adverse reactions, including fatalities in dogs, may occur, especially Collies, Old English Sheepdogs and related breeds and crosses. Do not use in animals with a known sensitivity to the active ingredient or to any of the excipients.
Transient discomfort has been observed in some cattle following subcutaneous administration. A low incidence of soft tissue swelling at the injection site has been observed. These reactions disappeared without treatment. If you notice any serious effects or other effects not mentioned in this leaflet, please inform your veterinary surgeon.
Care should be taken to avoid the following practices because they increase the risk of development of resistance and could ultimately result in ineffective therapy:
- Too frequent and repeated use of anthelmintics from the same class, over an extended period of time.
- Underdosing, which may be due to underestimation of body weight, misadministration of the product, or lack of calibration of the dosing device (if any).
Suspected clinical cases of resistance to anthelmintics should be further investigated using appropriate tests (e.g. Faecal Egg Count Reduction Test). Where the results of the test(s) strongly suggest resistance to a particular anthelmintic, an anthelmintic belonging to another pharmacological class and having a different mode of action should be used.
This product does not contain any antimicrobial preservative - swab septum before removing each dose.
To avoid secondary reactions due to the death of Hypoderma larvae in the oesophagus or the spine, it is recommended to administer the product at the end of the period of fly activity and before the larvae reach their resting sites: seek professional advice on the correct timing of treatment.
Divide doses in excess of 10 ml between different injection sites and use different sites to those used for other parenteral medications.
Treated cattle should not have direct access to ponds, streams or ditches for 14 days after treatment.
Pregnancy, lactation and fertility
Can be used in pregnancy and lactation. Can be used in breeding animals.
Overdose (symptoms, emergency procedures, antidotes)
A dose of 25ml product per 50kg bodyweight (25 times the recommended dose level) may result in an injection site lesion, including tissue necrosis, oedema, fibrosis and inflammation.
Interaction with other medicinal products and other forms of interaction
Do not smoke or eat whilst handling the product. Wash hands after use.
Take care to avoid self-injection: the product may cause local irritation and/or pain at the injection site. In case of accidental self-injection, seek medical advice and show the label to the doctor.
Direct contact with the skin should be avoided.
In the absence of compatibilities studies, this veterinary medicinal product must not be mixed with other veterinary medicinal products.
Special precautions for the disposal of unused product or waste material if any
EXTREMELY DANGEROUS TO FISH AND AQUATIC LIFE. Do not contaminate surface waters or ditches with the product or used container. Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal products should be disposed of in accordance with local requirements.
Meat and offal: 66 days.
Milk: Do not use in cattle producing milk for human consumption. Do not use in non-lactating dairy cows including pregnant heifers within 60 days of calving.
Protect from light. Keep the container in the outer carton in order to protect from light.
Shelf-life of the veterinary medicinal product after withdrawal of the first dose: 28 days.Discard unused material.
Legal category: POM-VPS
50ml, 250ml and 500ml containers