Category: A
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-VPS |
| Temperature | Ambient |
| MA/VM/EU No: | 11990/4054 |
| Species |
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| VMD Link | https://www.vmd.defra.gov.uk/ProductInformationDatabase/product/A007231 |
| NOAH Link | https://www.noahcompendium.co.uk/?id=-449002&fromsearch=true#iosfirsthighlight |
| Dosage | Dosage: 1ml per 50 kg bodyweight by subcutaneous injection (based on a recommended dosage level of 200 |
| Withdrawals | Do not use this product intravenously or intramuscularly. Animec Super Injection is a low volume product authorised for use in cattle. It must not be used in other species as severe adverse reactions, including fatalities in dogs, may occur, especially Collies, Old English Sheepdogs and related breeds and crosses. Do not use in animals with a known sensitivity to the active ingredient or to any of the excipients. Special warnings Care should be taken to avoid the following practices because they increase the risk of development of resistance and could ultimately result in ineffective therapy: - Too frequent and repeated use of anthelmintics from the same class, over an extended period of time. - Underdosing, which may be due to underestimation of body weight, misadministration of the product, or lack of calibration of the dosing device (if any). Suspected clinical cases of resistance to anthelmintics should be further investigated using appropriate tests (e.g. Faecal Egg Count Reduction Test). Where the results of the test(s) strongly suggest resistance to a particular anthelmintic, an anthelmintic belonging to another pharmacological class and having a different mode of action should be used. Special precautions for use in animals This product does not contain any antimicrobial preservative - swab septum before removing each dose. To avoid secondary reactions due to the death of Hypoderma larvae in the oesophagus or the spine, it is recommended to administer the product at the end of the period of fly activity and before the larvae reach their resting sites: seek professional advice on the correct timing of treatment. Divide doses in excess of 10 ml between different injection sites and use different sites to those used for other parenteral medications. Special precautions to be taken by the person administering the veterinary medicinal product to animals Do not smoke or eat whilst handling the product. Wash hands after use. Take care to avoid self-injection: the product may cause local irritation and/or pain at the injection site. In case of accidental self-injection, seek medical advice and show the label to the doctor. Direct contact with the skin should be avoided. Other precautions Treated cattle should not have direct access to ponds, streams or ditches for 14 days after treatment. Adverse reactions Transient discomfort has been observed in some cattle following subcutaneous administration. A low incidence of soft tissue swelling at the injection site has been observed. These reactions disappeared without treatment. If you notice any serious effects or other effects not mentioned in this leaflet, please inform your veterinary surgeon. Pregnancy, lactation and fertility Can be used in pregnancy and lactation. Can be used in breeding animals. Overdose (symptoms, emergency procedures, antidotes) A dose of 25ml product per 50kg bodyweight (25 times the recommended dose level) may result in an injection site lesion, including tissue necrosis, oedema, fibrosis and inflammation. Interaction with other medicinal products and other forms of interaction None known. Incompatibilities In the absence of compatibilities studies, this veterinary medicinal product must not be mixed with other veterinary medicinal products. Withdrawal periods Meat and offal: 66 days. Milk: Do not use in cattle producing milk for human consumption. Do not use in non-lactating dairy cows including pregnant heifers within 60 days of calving. |
