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Date: Saturday, May 18, 2024 10:47

Description: 2015-Elanco-logo
Telephone: 01256 353131 (24 hr response) Veterinary Technical Services
Release 2.58
Stellamune Once
 
Species: Pigs
Therapeutic indication: Immunological veterinary medical products: For pigs
Active ingredient: Vaccine Antigens
Product:Stellamune Once
Product index: Stellamune Once
Pig - meat: Zero days
Incorporating:
Qualitative and quantitative composition
Per 2 ml dose:
Active substance:
Inactivated Mycoplasma hyopneumoniae, strain NL1042, between 4.5 and 5.2 log10 units*.
*ELISA Relative Potency Units by comparison with a reference vaccine.
Adjuvant:
Amphigen Base 0.025 ml
Drakeol 5 (Mineral oil) 0.075 ml
Excipient(s):
Thiomersal 0.185 mg
For a full list of excipients, see section Pharmaceutical Particulars
Pharmaceutical form
Emulsion for injection
Off white, translucent, semi turbid oil in water emulsion
Clinical particulars
Target species
Fattening pigs
Indications for use, specifying the target species
For active immunisation of piglets from 3 days of age to reduce lung lesions related to infection by Mycoplasma hyopneumoniae in fattening animals.
Onset of immunity : 18 days following vaccination.
Duration of immunity : 26 weeks following vaccination.
For active immunisation of piglets from 3 weeks of age to reduce coughing and losses in weight gain related to infection by Mycoplasma hyopneumoniae in fattening animals.
Onset of immunity : 3 weeks following vaccination.
Duration of immunity : 23 weeks following vaccination
Contraindications
None
Special warnings
None.
Special precautions for use
Special precautions for use in animals
None.
Special precautions to be taken by the person administering the veterinary medicinal product to animals
To the user:
This product contains mineral oil. Accidental injection/self injection may result in severe pain and swelling, particularly if injected into a joint or finger, and in rare cases could result in the loss of the affected finger if prompt medical attention is not given.
If you are accidentally injected with this product, seek prompt medical advice even if only a very small amount is injected and take the package leaflet with you.
If pain persists for more than 12 hours after medical examination, seek medical advice again.
To the physician:
This product contains mineral oil. Even if small amounts have been injected, accidental injection with this oil-based product can cause intense swelling, which may, for example, result in ischaemic necrosis and even the loss of a digit. Expert, PROMPT, surgical attention is required and may necessitate early incision and irrigation of the injected area, especially where there is involvement of finger pulp or tendon.
Adverse reactions (frequency and seriousness)
Local tissue reactions in the form of a transient swelling at the injection site (max. diameter 2.5 cm) are very common (more than 1 in 10 animals) and may last for up to 3 days
Transient increase in rectal temperature (up to 1.9°C above baseline) can be observed for up to 4 days post vaccination.
As part of the immune reaction following vaccination, inflammatory cell infiltration and/or fibrosis may occur in the muscle tissue at the injection site lasting for at least 14 days.
Hypersensitivity reactions, including shock and death may occur in very rare cases. Appropriate treatment (for example glucocorticoid intravenously or adrenaline intramuscularly) should be administered.
Use during pregnancy, lactation or lay
The safety of the veterinary medicinal product has not been established during pregnancy or lactation.
Interaction with other medicinal products and other forms of interaction
No information is available on the safety and efficacy of this vaccine when used 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.
Amounts to be administered and administration route
Shake and aseptically administer a single 2 ml injection by deep intramuscular route in the lateral neck muscle. Needle length and diameter should be adapted to the age of the animals.
Vaccination programme:
One single dose of 2 ml of vaccine should be given.
Vaccination should be performed prior to the period of risk. Infection usually occurs within the first month of life.
Overdose (symptoms, emergency procedures, antidotes), if necessary
Injection site reactions observed after the administration of one overdose are similar to those following a single dose of vaccine. Very commonly (more than 1 in 10 animals), animals vaccinated with an overdose develop a palpable injection site reaction of up to 3 cm in diameter that resolves within 2 days.
A lower growth rate has been observed in animals administered a double dose of vaccine.
Withdrawal period
Zero days.
Pharmacological particulars
To stimulate active immunity against Mycoplasma hyopneumoniae in pigs.
ATC Vet Code QI09AB13.
Pharmaceutical particulars
List of excipients
Thiomersal
Polysorbate 80
Sorbitan oleate
Disodium EDTA
Phosphate buffered saline
Incompatibilities
Do not mix with any other veterinary medicinal product.
Shelf life
Shelf life of the veterinary product as packaged for sale: 3 years.
Shelf-life after first opening the immediate packaging: 10 hours
Special precautions for storage
Store in a refrigerator (2°C – 8°C).
Protect from light.
Do not freeze.
A slight black deposit may appear during storage.
Nature and composition of immediate packaging
High Density Polyethylene vials containing 10, 50 or 125 doses of liquid component, respectively 20, 100 or 250 ml. Chlorobutyl rubber closures.
Packaging intended for sale are: box of 10 vials of 10 doses, box of 10 vials of 50 doses and box of 4 vials of 125 doses.
Not all pack sizes may be marketed.
Special precautions for the disposal of unused veterinary medicinal product or waste materials derived from the use of such products
Any unused veterinary medicinal product or waste material derived from such veterinary medicinal product should be disposed of in accordance with local requirements.
Marketing Authorisation Holder (if different from distributor)
N/A
Marketing Authorisation Number
Vm 00879/4202
Significant changes
Date of the first authorisation or date of renewal
10 September 2001
Date of revision of the text
July 2020
Any other information
Legal category
Legal category: POM-V
GTIN
GTIN description:Stellamune Once 10 x 50 doses
GTIN:05013457078831