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PROGRESSIS®
QUALITATIVE AND QUANTITATIVE COMPOSITION

Each 2-ml dose of vaccine contains: inactivated PRRS virus in an oily adjuvant.

  • Active substance:Inactivated Porcine Reproductive and Respiratory Syndrome (PRRS) virus, P120 strain
  • Adjuvant: O/w oily
  • excipient (containing hydrogenated polyisobutene as adjuvant)
PHARMACEUTICAL FORM

Emulsion for injection.

Target species

Pigs (sows and gilts).

Indications for use, specifying the target species

Reduction of the reproductive disorders caused by Porcine Reproductive and Respiratory Syndrome virus (European strain) in a contaminated environment: vaccination reduces the number of early farrowings and the number of still-births.

Contraindications

None.

Special warnings for each target species

In PRRS infected herds, viral infection is heterogeneous and varies over time.

In such context, the implementation of a vaccination program is a tool to improve the reproductive parameters and may contribute to the disease control in conjunction with sanitary measures.

Special precautions for use
  • Vaccinate only healthy animals.
  • Apply usual procedures for the handling of animals
  • Special precautions to be taken by the person administering the veterinary medicinal product to animals To the user: This product contains mineral oil.
  • Do not mix with any other veterinary medicinal product.
  • Store in a refrigerator (2 °C – 8 °C)
  • Do not freeze. Protect from light
Adverse reactions

Vaccination may induce a transient oedema (at most 3 cm) lasting generally less than one week and small local reaction (granulomas), without any effect on the health and the reproductive performance of the animal.

Vaccination may rarely cause hypersensitivity reactions. In such cases, an appropriate symptomatic treatment should be carried out.

Use during pregnancy, lactation or lay

Can be used during pregnancy and lactation

Interaction with other medicinal products and other forms of interaction

Data are available which demonstrate that this vaccine can be administrated on a same day in a separate site, with inactivated vaccines against parvovirosis, influenza and Aujeszky’s disease as no adverse effect on the serological response has been observed

No information is available on the safety and efficacy of this vaccine when used with any other veterinary medicinal product except the products mentioned above.

Amounts to be administered and administration route

Apply usual aseptic procedures.

One dose of 2 ml is administered by deep intramuscular route, in the neck muscles behind the ear, according to the following vaccination scheme:

Primary vaccination:

Gilts: 2 injections 3-4 weeks apart, at least 3 weeks before mating.

Sows: 2 injections 3-4 weeks apart (vaccination of all the sows of the herd within a short period is recommended).

Revaccination:

One injection at 60-70 days of each gestation, as of the first gestation following the primary vaccination.

Withdrawal period(s)

Zero days.

Shelf-life of the veterinary medicinal product as packaged for sale:18 months.

Shelf life after first opening the vial: use immediately after opening.


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GENERAL REMINDER:
Product indications, usage instructions & withdrawal periods may vary by Country.
Always follow label instructions and consult your veteriarian or pig health adviser.

This page contains information on veterinary pharmaceutical and biological products that are sold in several different countries and areas where they may be marketed under different trade names and pursuant to different regulatory approvals. Accordingly, ThePigSite and CEVA SANTE ANIMALE give no guarantee that the details presented are correct with respect to all locations.

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