Mycosalmovir®

 Description

Inactivated vaccine against salmonellosis, paramyxovirosis and mycoplasmosis in pigeons

STATEMENT OF ACTIVE AND OTHER SUBSTANCES

Each dose of the vaccine (0.2 ml) contains:

inactivated PMV-1 (LaSota strain), no less than 1 Elisa unit

inactivated Mycoplasma gallisepticum cells, no less than one Elisa unit

inactivated Salmonella cells (serotypes: S. typhi. S. paratyphi. A, S. paratyphi. C, S. typhimurium var. Copenhagen, S. anatum, S. senftenberg), no less than 1 Elisa unit for each serotype

1Elisa unit – the quantity of antigen to obtain seroconversion equal or higher than 1.8 in a vaccinated pigeon

Adjuvant:

Adjuvant Montanide ISA 763A VG 0.14ml

INDICATIONS
Active immunisation of pigeons to decrease the mortality rate and clinical symptoms of salmonellosis, mycoplasmosis and paramyxovirosis of pigeons.

The postvaccinal immunity occurs approx. 21 days after the re-vaccination and lasts for approx. 12 months.

CONTRAINDICATION
Do not immunise weak, infested and sick birds.
Do not use in the moulting period of pigeons.

ADVERSE EFFECTS
Rarely reported adverse reactions include a transitional lack of appetite and apathy, occurring within several hours from administration, as well as a transitional local reaction in the form of insignificant nodules.

Should any adverse effects or any reactions not mentioned in the leaflet occur (including reactions in humans due to contact with the preparation), please contact your veterinarian or inform the marketing authorisation holder or the Office for Registration of Medicinal Products, Medical Devices and Biocides. The application form can be downloaded from the website: http://www.urpl.gov.pl (Department of Medicinal Veterinary Products).

DOSAGE FOR EACH SPECIES, ROUTES AND METHOD OF ADMINISTRATION
The vaccine is used in pigeons from the age of 3 - 4 weeks. The basic vaccination of young pigeons not immunised against salmonellosis, paramyxovirosis and mycoplasmosis includes two injections, with a four-week interval. The vaccination should be planned in such a way that the second administration of the vaccine does not take place later than three weeks before migration. The vaccination of adult pigeons, which were immunised with the vaccine Mycosalmovir several times, should be conducted annually 2-3 weeks before mating and exhibitions. The dose for one pigeon is 0.2 ml of the oil emulsion, which should be injected subcutaneously in the middle of the neck. Use sterile needles and syringes for vaccinations.

ADVICE ON CORRECT ADMINISTRATION
Warm the packages with the vaccine to room temperature after taking them from a refrigerator and mix the contents thoroughly before starting the procedure.
During the vaccination procedure, mix the content of the package regularly.
Conduct the procedures at an ambient temperature not lower than 00C.
Once opened, the product cannot be stored and used again.

WITHDRAWAL PERIOD
Zero days. 

SPECIAL STORAGE AND TRANSPORT PRECAUTIONS
Keep out of the reach and sight of children.
Store in a refrigerator (2-8oC). Do not freeze! Protect from light.
Once opened, use immediately.
Do not use after the expiry date which is stated on the label.

SPECIAL WARNINGS
For the user:
The product contains mineral oil. Accidental injection may result in pain and swelling, especially in the case of injection into the joint of a finger. Without immediate doctor's attention, such a situation may end in the amputation of the finger. Therefore, in the case of an accidental injection of even a slight quantity of the product, contact your doctor immediately and show the informational leaflet. If the pain lasts longer than 12 hours after medical attention, consult your doctor once again.

For the medical practitioner:
The product contains mineral oil. Even if a slight amount of the product has been injected accidentally, it may lead to great pain and swelling, and, as a consequence, to ischemic necrosis and the necessity of amputation. Professional and QUICK surgical intervention is absolutely necessary. Such an operation may involve an incision and irrigation of the injection site, especially when it is the finger bulb or tendon.

No information is available on the safety and efficacy from the concurrent use of this vaccine with any other. It is therefore recommended that no other vaccines should be administered within 14 days before and after the administration of this product.

After the administration of a double dose, no other undesirable effects occurred than those specified in the section concerning adverse reactions.

Do not mix with any other veterinary medicinal product.

SPECIFIC PRECAUTIONS FOR THE DISPOSAL OF UNUSED PRODUCTS OR WASTE MATERIALS
Medicines should not be disposed of via wastewater or household waste.

Ask your veterinary surgeon how to dispose of medicines no longer required. These measures should help to protect the environment.

FURTHER INFORMATION
Package size: 20 doses, 50 doses, 100 doses

For any information about this veterinary medicinal product, please contact the local representative of the marketing authorisation holder.

SHELF-LIFE
18 months.
The contents of a package must be used within one day.

WARNING
Do not allow to freeze.

 More details

Name Description
Place of Origin: Poland

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 24-100 Pulawy, Arciucha 2 NIP 716-11-26-796 Biowet Pulawy Ltd.,Poland, Europe
 3 years, 5 months ago
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