Bimectin Plus
ATC code
Species
Cattle
Indications
The product is indicated for the treatment of mixed trematode and nematode or arthropod infestations of the following parasites:
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
Oesophagostamum radiatum
Strongyloides papillosus (adult)
N. spathiger (adult)
N. helvetianus (adult)
Lungworms (adult and fourth-stage larvae)
Dictyocaulus viviparous
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 control of biting lice (Damalinia bovis) and the mange mite Chorioptes bovis, but complete elimination may not occur.
Persistent activityThe product given at the recommended dosage of 1ml/50kg 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
200μg ivermectin and 2mg clorsulon per kg bodyweight corresponding to a single dose of 1ml per 50kg 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 in excess of 10 ml between different injection sites and use different sites to those used for other parenteral medications.
A sterile 17 gauge ½ inch (15-20mm) needle is recommended. Replace with a fresh sterile needle after every 10-12 animals or sooner if the needle becomes soiled.
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.
When using the 500ml pack size use only automatic syringe equipment. For the 50ml 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, body weight 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.
Adverse reactions
Transitory 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.
Dispensing
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Art. Nr. | 50146/4003 |
EAN | 5391510234524 |