Product Ref: UPEXC04 Category: E
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Category | POM-V |
Temperature | Ambient |
MA/VM/EU No: | 42058/4065 |
Species |
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VMD Link | https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_179387.PDF |
NOAH Link | |
Dosage | Amounts to be administered and administration route Before use, shake the bottle vigorously for a maximum of 60 seconds or until the product appears adequately resuspended. To ensure a correct dosage, bodyweight should be determined as accurately as possible to avoid underdosing. Pigs: 3 mg ceftiofur /kg bw/day for 3 days via intramuscular route, i.e. 1 ml/16 kg bw at each injection. Not more than 4 ml should be administered per injection site. Cattle: Respiratory disease: 1 mg ceftiofur /kg bw/day for 3 to 5 days by subcutaneous injection, i.e. 1 ml/50 kg bw at each injection. Acute interdigital necrobacillosis: 1 mg/kg bw/day for 3 days by subcutaneous injection, i.e. 1 ml/50 kg bw at each injection. Acute post-partum metritis within 10 days after calving: 1 mg/kg bw/day for 5 consecutive days by subcutaneous injection, i.e. 1 ml/50 kg bw at each injection. Not more than 13 ml should be administered per injection site. In case of acute post-partum metritis, additional supportive therapy might be required in some cases. Subsequent injections must be given at different sites. 50 ml and 100 ml vials can be broached a maximum of 50 times. 250 ml vials can be broached a maximum of 33 times. Otherwise, the use of a multiple-dose syringe is recommended. 4.10 Overdose (symptoms, emergency procedures, antidotes), if necessary The low toxicity of ceftiofur has been demonstrated in pigs using ceftiofur sodium at doses in excess of 8 times the recommended daily dose of ceftiofur intramuscularly administered for 15 consecutive days. In cattle, no signs of systemic toxicity have been observed following substantial parenteral overdosages. |
Withdrawals | Pigs: meat and offal: 2 days. Cattle: meat and offal: 6 days; milk: zero hours. |