STATEMENT OF ACTIVE SUBSTANCES AND OTHER INGREDIENTS
Ivermectin 10mg/ml, Clorsulon 100mg/ml.
INDICATIONS
Treatment of infestations with adult trematodes, liver flukes and gastrointestinal nematodes, lung flukes, eye flukes and/or lice and ticks in beef cattle or non-lactating dairy cows.
Animec Super injectable solution for cattle treats:
Persistent activity
When cattle have to graze on pasture infested with nematode larvae.
It can be used as an adjunct in the treatment of malophagous lice (Damalinia bovis) and mange mites Chorioptes bovis, but elimination may not occur.
CONTRAINDICATIONS
This product is not for intravenous or intramuscular use. This product is a low volume product authorised for use in cattle. Do not use in other species as severe adverse reactions, including death, may occur, particularly in Collies, Old English Sheepdogs and related or cross-breeds. Do not use in case of hypersensitivity to the active substances or to any of the excipients.
Adverse reactions:
A transient discomfort was observed in some cattle after subcutaneous administration. Rare cases of soft tissue inflammation at the injection site have also been observed.
These reactions disappeared without treatment. If you notice any serious reactions or other effects not mentioned in this leaflet, please inform your veterinarian.
TARGET SPECIES
Cattle.
DOSAGE FOR EACH SPECIES, ROUTE(S) OF ADMINISTRATION AND METHOD OF ADMINISTRATION
Animec Super injectable solution for cattle contains 1% w/v (10 mg/ml) ivermectin and 10% w/v (100 mg/ml) clorsulon in a sterile solution. The recommended dose is 1ml for every 50kg body weight by subcutaneous injection. This dose provides 200 ug ivermectin and 2 mg clorsulon per kg body weight.
DOSAGE AND ADMINISTRATION
Over 300kg administer 1 ml per 50 kg body weight. To ensure correct dosing, body weight should be determined as accurately as possible.
If animals are to be treated collectively and not individually, to avoid under or overdosing, they should be grouped according to body weight and the dose adjusted accordingly. Administer only by subcutaneous injection. Doses greater than 10 ml should be administered at two different injection sites. The treatment period should be based on epidemiological factors and should be adapted to each individual farm. A dosing schedule should be established by a qualified professional.
WITHDRAWAL PERIOD
Meat and offal: 66 days.
Milk: not authorised for use in animals producing milk for human consumption. Do not use in non-lactating cows, including pregnant heifers, within 60 days of calving.
SPECIAL STORAGE PRECAUTIONS
Keep out of the sight and reach of children. Protect from light. Store in the outer carton in order to protect from light.
Shelf life of the veterinary medicinal product after first opening the immediate packaging: 28 days. Discard any unused product.
SPECIAL WARNING
The following practices should be avoided as they may increase the risk of developing resistance and may ultimately result in ineffective treatment:
-Too frequent use and repeated use of anthelmintics from the same class for a long period of time.
-Underdosing which may be caused by underestimation of body weight or non-calibration of dosing devices (if applicable).
Clinical cases suspected of anthelmintic resistance should be further investigated by appropriate methods (ovocoproscopy, etc.). If the test results clearly indicate the establishment of resistance to a specific anthelmintic from another pharmacological class and which has a different mode of action. This product does not contain any antimicrobial preservative. Disinfect the bottle cap before withdrawing each dose. Doses greater than 10ml should be administered at two different injection sites for other parenteral preparations administered concurrently.
Precautions for the user
Do not smoke, drink or eat while handling the product. Wash hands after use. Avoid direct skin contact. 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 immediately and show the package leaflet or the label to the physician.
Treated cattle should not have direct access to ponds, watercourses or canals for 14 days after treatment.
Can be used during pregnancy and lactation. Can be used in breeding animals.
After a dose of 25 ml for every 50 kg body weight (25 times the recommended dose) lesions at the injection site, including tissue necrosis, oedema, fibrosis and inflammation, may occur.
SPECIAL PRECAUTIONS FOR DISPOSAL OF UNUSED PRODUCT OR WASTE MATERIALS, IF ANY
VERY HAZARDOUS TO FISH OR AQUATIC ORGANISMS
The product or its packaging must not be emptied into water courses.
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