País: Reino Unido
Idioma: inglés
Fuente: VMD (Veterinary Medicines Directorate)
Fenbendazole
C&H Generics Ltd
QP52AC13
Fenbendazole
Granules
AVM-GSL - Authorised Veterinary Medicine – General Sales List
Dogs
Anthelmintic
Expired
2016-08-17
Issued: August 2016 AN: 01702/2013 Page 1 of 4 SUMMARY OF PRODUCT CHARACTERISTICS 1. NAME OF THE VETERINARY MEDICINAL PRODUCT Fenbendazole Wormer Granules 888 mg for Adult Dogs 2. QUALITATIVE AND QUANTITATIVE COMPOSITION Each sachet contains: ACTIVE SUBSTANCE: Fenbendazole 888.8 mg EXCIPIENT(S): For the full list of excipients, see section 6.1. 3. PHARMACEUTICAL FORM Granules A free flowing white to greyish white granular powder 4. CLINICAL PARTICULARS 4.1 TARGET SPECIES Dogs. 4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES Dogs For the treatment of immature and mature stages of Toxacara canis and Taenia hydatigena. 4.3 CONTRAINDICATIONS Do not use in cases of known hypersensitivity to the active substance or the excipients. 4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES None 4.5 SPECIAL PRECAUTIONS FOR USE SPECIAL PRECAUTIONS FOR USE IN ANIMALS None Issued: August 2016 AN: 01702/2013 Page 2 of 4 SPECIAL PRECAUTIONS TO BE TAKEN BY THE PERSON ADMINISTERING THE VETERINARY MEDICINAL PRODUCT TO ANIMALS The product can cause irritation to the skin, eyes and lungs. Direct contact with the skin should be kept to a minimum. Avoid inhalation of granule dust. Wash hands after use. Avoid contact with the eyes. In case of accidental eye contact, irrigate the eyes with plenty of clean water. If irritation persists, seek medical advice. Only use for the bodyweight of animal recommended. The entire contents of the sachet must be directly sprinkled onto food as a single dose. Discard any uneaten medicated feed. 4.6 ADVERSE REACTIONS (FREQUENCY AND SERIOUSNESS) None known 4.7 USE DURING PREGNANCY, LACTATION OR LAY Not recommended. Seek the advice of a veterinary surgeon before using the product during pregnancy or lactation 4.8 INTERACTION WITH OTHER MEDICINAL PRODUCTS AND OTHER FORMS OF INTERACTION None known. 4.9 AMOUNTS TO BE ADMINISTERED AND ADMINISTRATION ROUTE For oral administration only; sprinkled onto food. For the routine treatment of adult dogs a dosage of 100 mg/kg is recommended. This equates to approximately 1 Leer el documento completo