Equip Rotavirus (10 doses)

Equip Rotavirus (10 doses)

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Item Number: EQUIPROTA 
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£488.69 (Incl. Vat)

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Equip Rotavirus emulsion for injection for horses.

For the vaccination of pregnant mares to provide passive transfer of antibodies to foals to reduce the risk of diarrhoea caused by equine rotavirus G3 P12 serotypes.
Mares are able to transfer the passive immunity to the foals 4 weeks after the third vaccination. Foals of the vaccinated mares show an increase in antibodies against equine rotavirus for approximately sixty days.

Dosage and administration
1.0 ml dose per mare to be administered by deep intramuscular injection.

Vaccination Schedule
Pregnant mares should be given three doses of vaccine consisting of a single 1ml dose administered at the 8th, 9th and 10th month of each pregnancy.

Contra-indications, warnings, etc
For animal treatment only.
Vaccinate healthy animals only.
Use of this vaccine in a mare can only aid the control of diarrhoea associated with rotavirus in its foal when the foal receives an adequate quantity of colostrum within 24 hours after birth and a continuous intake of milk derived from the vaccinated mare is ensured. Both the mare's ability to respond by the production of antibodies in colostrum and the ability of the foal to ingest and absorb that colostrum is required for the vaccine to have an effect.
Can be used during pregnancy.
The safety of the veterinary medicinal product has not been established during lactation.
No information is available on the safety and efficacy of this vaccine with any other veterinary medicinal product. 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.

Adverse Reactions:
In mares a transient increase (up to 1.8°C) in rectal temperature which may last up to 2 days following vaccination may be very commonly observed.
A small visible soft to firm swelling (2.5 = x = 3.5 cm) lasting generally for only two days may be commonly observed. The swelling may be painful for 1 - 2 days.
In most cases these small and transient injection site reactions resolve with no need for treatment.
The frequency of adverse reactions is defined using the following convention:
- very common (more than 1 in 10 animals displaying adverse reactions during the course of one treatment)
- common (more than 1 but less than 10 animals in 100 animals)
- uncommon (more than 1 but less than 10 animals in 1,000 animals)
- rare (more than 1 but less than 10 animals in 10,000 animals)
- very rare (less than 1 animal in 10,000 animals, including isolated reports).

Adverse events observed after administration of a double dose are similar to those following administration of a single dose as listed above.
If you notice any serious effects or other effects not mentioned in this leaflet, please inform your veterinary surgeon.

Operator Warning
In case of accidental self-injection, seek medical advice immediately and show the package leaflet or the label to the physician.

Withdrawal Period
Zero days.

Pharmaceutical precautions
Store and transport refrigerated (2°C - 8°C).
Do not freeze. Protect from light.
Do not use after the expiry date printed on the syringe.
Keep out of the sight and reach of children.
For animal treatment only.

Legal category
Legal category: POM-V

Packaging quantities
Syringes are supplied in packs of 3, 10, 20 and 40 units.
Not all pack sizes may be marketed.
Further information

Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal products should be disposed of in accordance with local requirements.


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