Blackleg Vaccine 50Ml (Zoetis)

   Product Ref: PMBLA01 Category: B

13.66


Vat Rate: 20%

Animal Details Required



For the active immunisation of cattle and sheep against disease associated with infections caused by Clostridium chauvoei (Blackleg and post-parturient gangrene). Onset and duration of immunity have not been determined for this vaccine.
Vat Rate: 20%

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.

 

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Category POM-VPS
Temperature Refrigerated
MA/VM/EU No: 42058/4010
Species
  • cattle
  • sheep
VMD Link https://www.vmd.defra.gov.uk/ProductInformationDatabase/product/A002919
NOAH Link https://www.noahcompendium.co.uk/?id=-456528
Dosage Administration By subcutaneous injection, preferably in the loose skin on the side of the neck, observing aseptic precautions. Shake bottle thoroughly before use. Syringes and needles should be sterilised before use and the injection should be made through an area of clean, dry skin, taking precautions against contamination. Primary vaccination Cattle: two doses of 2 ml administered six weeks apart, 2-3 weeks before the expected period of risk. Sheep: two doses of 1 ml administered six weeks apart, 2-3 weeks before the expected period of risk. Revaccination Revaccination with a single dose is advised annually before the expected period of risk.
Withdrawals Do not vaccinate sick or immunodeficient animals. No side effects other than those listed below are expected when the vaccine is used between 8 and 2 weeks prior to parturition. In the absence of specific data, the use of the vaccine during the first or second trimester of pregnancy should be avoided. Avoid stress in pregnant ewes and cows. Clinical trials have demonstrated that the presence of maternal antibodies against C. chauvoei may reduce the antibody response to vaccination in young lambs. Therefore, to ensure an optimal response in young animals with high levels of MDA, the primary vaccination should be delayed until the levels wane (which is after about 8-12 weeks of age). In the event of an anaphylactic reaction appropriate treatment, such as adrenaline, should be administered without delay. Most vaccinated animals may experience reactions to vaccination. These reactions are usually localised swelling (up to 14 cm in diameter, which resolves in less than 10 weeks) or induration at the injection site but may also include abscess (in up to 17% of animals) or other reaction in underlying tissues at the injection site. Skin discolouration (which returns to normal as the local reaction resolves) and localised pain for 1-2 days post first vaccination may occur at the injection site. The local reactions do not affect the general health, demeanour, feeding or weight gain of the animals. No information is available on the safety and efficacy from the concurrent use of this vaccine with any other. A decision to use this vaccine before or after any other veterinary medicinal product therefore needs to be made on a case by case basis. Do not mix with any other veterinary medicinal product. Withdrawal periods Cattle: zero days. Sheep: zero days. Operator warnings In the case of accidental self-injection, encourage bleeding and wash the area immediately with water. If a local reaction develops, seek medical advice showing the package leaflet or the label to the physician.