Country: United Kingdom
Language: English
Source: VMD (Veterinary Medicines Directorate)
Fenbendazole
MSD Animal Health UK Limited
QP52AC13
Fenbendazole
Continuous-release intraruminal device
POM-VPS -Prescription Only Medicine – Veterinarian, Pharmacist, Suitably Qualified Person
Cattle
Anthelmintic
Authorized
1995-12-01
Revised: December 2020 AN: 01394/2020 Page 1 of 6 SUMMARY OF PRODUCT CHARACTERISTICS 1. NAME OF THE VETERINARY MEDICINAL PRODUCT Panacur Bolus 12 g, Continuous Release Intraruminal Device 2. QUALITATIVE AND QUANTITATIVE COMPOSITION Active substances Each 12 g intraruminal device contains: Qualitative composition Quantitative composition in g Fenbendazole 12 Excipients For full list of excipients, see section 6.1 3. PHARMACEUTICAL FORM Continuous Release Intraruminal Device. A cylindrical intraruminal device, consisting of 10 grey/black flat-faced intraruminal devices in a magnesium alloy tube, enclosed by plastic rings. 4. CLINICAL PARTICULARS 4.1 TARGET SPECIES Cattle 4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES The intraruminal device treats and prophylactically controls gastrointestinal nematode infections in cattle caused by _Ostertagia _spp., _Trichostrongylus _ spp., _Haemonchus _spp., _Cooperia _spp and _Oesophagostomum _spp. The intraruminal device aids in the control of parasitic bronchitis caused by _Dictyocaulus viviparus._ For use in ruminating cattle in their first grazing season weighing between 100kg and 300kg on the day of administration. When administered at turnout, the intraruminal device controls parasitic gastroenteritis throughout the grazing season by reducing the build up of infective larvae on the pasture. Reduced pasture contamination in the autumn lowers the risk of inhibited _Ostertagia_ larvae accumulating in sufficient numbers to cause winter ostertagiasis. When administered later in the season, the intraruminal device is effective in the treatment of established parasitic infections and continues to Revised: December 2020 AN: 01394/2020 Page 2 of 6 have a prophylactic effect up to 140 days after administration. This period may be reduced if cattle are moved to heavily infected pasture. 4.3 CONTRA-INDICATIONS Do not use in pre-ruminating cattle, cattle weighing less than 100kg or cattle less than 3 months of age. Do not administer to cattle over 300kg. 4.4 SPECIAL WARNING F Read the complete document