Product Ref: PFRIM17 Category: R
Royal Mail 2nd Class / Parcel Force 48
UK to UK :Normally arrives in 2-4 business days.
UK to Ireland :Normally arrives in 4-6 business days
UK to EU Countries : Normally arrives in 6-10 working days depending on where the parcel is going
Please note standered delivery is none trackable , none insured , no responsabily for lose or Damage
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Royal Mail First Class / Parcel Force 24
UK to UK :Normally arrives in 1-2 business days.
UK to Ireland 3-4 business days
UK to EU Countries : Normally arrives in 6-10 working days depending on where the parcel is going
Please note :Trackable , Royal Mail insured up to £50.
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Parcel Force Express AM Guaranteed before Midday.
UK to UK only . UP to 5KG Max Weight
Arrives next day before 12 noon, requires a signature.
Parcel Forcel Terms & Conditions apply
Important: Parcel Force advise that there are some postcodes where an extended delivery time exists, and may affect the date of delivery or the service is not available.
Category | POM-V |
Temperature | Ambient |
MA/VM/EU No: | 42058/4118 |
Species |
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VMD Link | Product Information Database (defra.gov.uk) |
NOAH Link | https://www.noahcompendium.co.uk/?id=-458138 |
Dosage | Administer Rimadyl Cattle as a single subcutaneous or intravenous injection at a dosage of 1.4 mg carprofen per kg bodyweight (1 ml/35 kg) in combination with antibiotic therapy as appropriate. When treating groups of animals, use a draw-off needle to avoid excessive broaching of the stopper. The maximum number of broaching should be limited to 20. |
Withdrawals | Do not use in animals suffering from cardiac, hepatic or renal impairment. Do not use in animals suffering from gastro-intestinal ulceration or bleeding. Do not use where there is evidence of a blood dyscrasia. Do not use in cases of known hypersensitivity to the active substance or to any of the excipients. Avoid use in any dehydrated, hypovolaemic or hypotensive animal, as there is a potential risk of increased renal toxicity. Concurrent administration of potentially nephrotoxic drugs should be avoided. Do not exceed the stated dose or the duration of treatment. Do not administer other NSAIDs concurrently or within 24 hours of each other. As NSAID therapy can be accompanied by gastro-intestinal or renal impairment, adjunctive fluid therapy should be considered especially in the case of acute mastitis treatment. No significant drug interactions have been reported for carprofen. During clinical studies in cattle four different antibiotic classes were used, macrolides, tetracyclines, cephalosporins and potentiated penicillins without known interactions. In common with other NSAIDs, carprofen should not be administered simultaneously with another veterinary medicinal product of the NSAID or glucocorticoid class. NSAIDs are highly bound to plasma proteins and may compete with other highly bound drugs, such that concomitant administration may result in toxic effects. However, during clinical studies in cattle four different antibiotic classes were used; macrolides, tetracyclines, cephalosporins and potentiated penicillins without known interactions. Studies in cattle have shown that a transient local reaction may form at the site of the injection. Withdrawal period Cattle (meat): 21 days. Cattle (milk): Zero days. User warnings Carprofen, in common with other NSAIDs, has been shown to exhibit photosensitizing potential in laboratory studies. Avoid skin contact with Rimadyl Cattle. Should this occur, wash the affected areas immediately. |