Animec Super
ATC code
Species
Cattle
Indications
For the treatment of mixed infestation of adult liver fluke and gastro-intestinal roundworms, lungworms, eye worms, and/or mites and lice of beef and non-lactating dairy cattle.
Gastrointestinal Roundworms (adult and fourth-stage larvae):
Ostertagia ostertagi (including inhibited larval stages)
O. lyrata
Haemonchus placei
Trichostrongylus axei
T. colubriformis
Cooperia oncophora
C. punctata
C. pectinata
Bunostomum phlebotomum
Oesophagostomum radiatum
Strongyloides papillosus (adult)
Nematodirus helvetianus (adult)
Nematodirus spathiger (adult)
Trichuris spp. (adult)
Lungworm (adult and fourth-stage larvae): Dictyocaulus viviparus
LIVER FLUKE (ADULT):
Fasciola hepatica EYE WORMS (ADULT):
Thelazia spp.
Warbles (parasitic stages):
Hypoderma bovis
H. lineatum
MANGE MITES:
Psoroptes bovis
Sarcoptes scabiei var. bovis
Sucking Lice:
Linognathus vituli
Haematopinus eurysternus
Solenopotes capillatus
The product may also be used as an aid in the treatment of biting lice (Damalinia bovis) and the mange mite Chorioptes bovis, but complete elimination may not occur.
Persistent Activity
The product given at the recommended dosage of 1 ml/50 kg bodyweight controls reinfection with Haemonchus placei, Cooperia spp. and Trichostrongylus axei, acquired up to 14 days after treatment, Ostertagia ostertagi and Oesophagostomum radiatum acquired up to 21 days after treatment and Dictyocaulus viviparus acquired up to 28 days after treatment.
Dose to be administered and administration route
Dosage and duration of treatment
For subcutaneous use.
A single dose of 1ml of the product per 50kg bodyweight, i.e. 200µg ivermectin and 2mg clorsulon per kg bodyweight.
Method of administration
The product should be administered only by subcutaneous injection under the loose skin in front of or behind the shoulder.
Divide doses greater than 10ml between two injection sites. A sterile 17 gauge (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 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.
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 overdosing, they should be grouped according to their bodyweight and dosed accordingly.
When the temperature of the product is below 5°c, difficulty in administration may be encountered due to increased viscosity. Warming the product and injection equipment to about 15°c will greatly increase the ease with which the product can be injected.
Adverse reactions
Transient discomfort has been observed in some cattle following subcutaneous administration. A low incidence of soft tissue swelling at the site of injection has been observed. These reactions disappeared without treatment.
PRICE | Only for registered vets. Create a free profile to access all features.. Login |
---|---|
Art. Nr. | 11990/4054 |