Product Ref: NBCOM15 Category: C
Royal Mail Tracked 24 (Signed For)
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Category | POM-V |
Temperature | Ambient |
MA/VM/EU No: | 02000/4238 |
Species |
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VMD Link | https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_140172.PDF |
NOAH Link | |
Dosage | Amount(s) to be administered and administration route For intramuscular injection at a dosage rate of 8.75 mg/kg bodyweight (1 ml per 20 kg bodyweight) daily for 3-5 days. Shake the vial well before use. After injection, massage the injection site. Use a completely dry sterile needle and syringe. Swab the septum before removing each dose. For Combined Therapy the following minimum treatment regime should be followed: Combiclav Injection Combiclav LC Intramammary 8.75 mg/kg bodyweight (7.0 mg amoxicillin, 1.75 mg clavulanic acid) i.e. 1 ml/20 kg bodyweight. One syringe gently infused into the teat of the infected quarter 24 hours Description: arrowdown 12 hours Description: arrowdown 8.75 mg/kg bodyweight (7.0 mg amoxicillin, 1.75 mg clavulanic acid) i.e. 1 ml/20 kg bodyweight. One syringe gently infused into the teat of the infected quarter 24 hours Description: arrowdown 12 hours Description: arrowdown 8.75 mg/kg bodyweight (7.0 mg amoxicillin, 1.75 mg clavulanic acid) i.e. 1 ml/20 kg bodyweight. One syringe gently infused into the teat of the infected quarter Where necessary Combiclav Injection may be administered for an additional two days for a total of 5 daily injections. To ensure the correct dosage, bodyweight should be determined as accurately as possible to avoid underdosing. Overdose (symptoms, emergency procedures, antidotes), if necessary Potentiated penicillin is of a low order of toxicity and is well tolerated by the parenteral route. Apart from occasional injection site reactions, which may occur at the recommended dose, no other adverse effects are to be expected from an accidental overdose. |
Withdrawals | Withdrawal period(s) Meat and offal: 42 days. Milk: 60 hours |