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Ovilis Enzovax x10
For the active immunisation of sheep against Chlamydia abortus.
Ovilis® Enzovax is indicated for the active immunisation of susceptible breeding female sheep as an aid in the prevention of abortion and stillbirth caused by Chlamydia abortus infection.
Ovilis® Enzovax is a live, attenuated vaccine, containing ≥ 105.0 IFU of Chlamydia abortus, strain TS 1B, per dose.
Dosage and administration
Ovilis® Enzovax should be reconstituted with Unisolve.
Remove approximately 5 ml of Unisolve from the vial with a syringe and needle. Inject into the vaccine vial and shake well until the powder plug is fully dissolved. Remove the solution from the vial, re-inject into the diluent vial and shake well. Take care not to generate an aerosol by ensuring that there are no air bubbles in the syringe before re-injecting into the vial.
The dose is a single injection of 2 ml of reconstituted vaccine by subcutaneous or intramuscular injection. Animals should be revaccinated after 2 years.
Ewe lambs intended for breeding may be vaccinated from 5 months of age. Shearlings and older ewes should be vaccinated in the 4 months before mating.
Withdrawal period: Animals should not be slaughtered for human consumption before 7 days after vaccination.
Vaccinate healthy animals only.
Do not vaccinate animals less than 4 weeks before mating.
Do not vaccinate pregnant animals.
Do not administer any other vaccine 14 days before or after vaccination with this product.
Do not open and reconstitute the vaccine until ready to start vaccination.
Do not mix Ovilis® Enzovax with other vaccines or medications.
Other live vaccines should not be administered within 4 weeks of the administration of Ovilis® Enzovax.
Dispose of any unused vaccine as well as all empty vaccine containers and vaccination equipment (e.g. gloves, needles and syringes used for mixing) according to local waste disposal regulations.
KEEP OUT OF REACH OF CHILDREN, UNINFORMED PERSONS AND ANIMALS.
Although this remedy has been extensively tested under a wide variety of conditions, failure thereof may ensue as a result of a wide range of reasons. If this is suspected, seek veterinary advice and notify the registration holder.
|Registration number||REG NL 8785|
|Legal status of supply||UDD|
|Route of administration||Intramuscular Injection (IM), Subcutaneous Injection (SC)|
|Withdrawal period||0 days|
|Units per outer box||0|