Patient leaflet - Equilis StrepE
B. PACKAGE LEAFLET
PACKAGE LEAFLET FOR:
Equilis StrepE, lyophilisate and solvent for suspension for injection, for horses
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1. NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER AND OF THE MANUFACTURING AUTHORISATION HOLDER RESPONSIBLE FOR BATCH RELEASE, IF DIFFERENT
Marketing authorization holder and manufacturer responsible for batch release:
Intervet International B.V.
Wim de Korverstraat 35
NL – 5831 AN Boxmeer
The Netherlands
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2. NAME OF THE VETERINARY MEDICINAL PRODUCT
Equilis StrepE, lyophilisate and solvent for suspension for injection, for horses
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3. STATEMENT OF THE ACTIVE SUBSTANCE AND OTHER INGREDIENT(S)
Per dose of 0.2 ml vaccine:
Live deletion mutant Streptococcus equi strain TW928 109.0 to 109.4 cfu1
1colony forming units
Lyophilisate: off-white or cream coloured pellet
Solvent: clear colourless solution
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4. INDICATION(S)
For immunisation of horses against Streptococcus equi to reduce clinical signs and occurrence of lymph node abscesses.
The onset of immunity is established as two weeks after vaccination. The duration of immunity is up to 3 months.
The vaccine is intended for use in horses for which a risk of Streptococcus equi infection has been clearly identified, due to contact with horses from areas where this pathogen is known to be present, e.g. stables with horses that travel to shows and/or competitions in such areas, or stables that obtain or have livery horses from such areas.
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5. CONTRAINDICATIONS
None.
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6. ADVERSE REACTIONS
After vaccination a diffusely swollen reaction, which may be warm or painful, develops at the injection site within 4 hours. The reaction is maximal at 2–3 days post vaccination with a maximum area of 3 cm by 8 cm. This swelling resolves completely within 3 weeks and normally has no effect on the appetite of the vaccinated animal and causes no apparent discomfort. The vaccine organism may establish a small suppurative inflammation locally at the injection site, leading to a disruption of the overlaying lip mucosa and subsequent discharge fluid and inflammatory cells. A slight cloudy discharge commonly occurs from the mucosal injection site at 3 or 4 days post vaccination.
Slight enlargements, which may be transient painful, of the retropharyngeal and mandibular lymph nodes may occur for a few days after vaccination. In very rare cases an abscess may develop at the injection site or in the regional lymph nodes.
Further, an increase in rectal temperature up to 2 °C may occur on the day of vaccination. In rare cases, inappetence, fever, shivering and diffuse oedematous swellings (e.g. facial oedema, swollen muzzle/upper lip) may be observed. In very rare cases depression may develop.
The frequency of adverse reactions is defined using the following convention:
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– very common (more than 1 in 10 animals displaying adverse reactions during the course of one treatment)
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– common (more than 1 but less than 10 animals in 100 animals)
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– uncommon (more than 1 but less than 10 animals in 1,000 animals)
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– rare (more than 1 but less than 10 animals in 10,000 animals)
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– very rare (less than 1 animal in 10,000 animals, including isolated reports).
If you notice any serious effects or other effects not mentioned in this leaflet, please inform your veterinary surgeon.
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7. TARGET SPECIES
Horses
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8. DOSAGE FOR EACH SPECIES, ROUTES AND METHOD OF ADMINISTRATION
Submucosal vaccination of 0.2 ml of reconstituted product.
Basic vaccination : Horses from 4 months of age onwards receive two vaccinations of one dose with a 4 week interval.
Revaccination: Revaccinate every three months to maintain immunity.
A priming response is maintained for up to six months after basic vaccination. Therefore only a single dose of vaccine is needed to restore immunity.
It is recommended that all horses stabled together are vaccinated.
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9. ADVICE ON CORRECT ADMINISTRATION
Allow the sterile solvent to reach room temperature (15–25 °C). Aseptically reconstitute the freeze-dried vaccine with 0.3 ml of the sterile solvent provided. Allow the reconstituted vaccine to sit for 1 minute and then carefully swirl the contents to mix. Do NOT shake. Withdraw 0.2 ml of the reconstituted vaccine into the syringe provided with the vaccine (see Figure 1) and connect the applicator to the needle (see Figure 2). Restrain the animal’s head, lift the upper lip and insert the needle into the inside of the upper lip until the applicator rests on the lip. Administer the whole contents of the syringe into the inside of the upper lip (see Figure 3).
Figure 1
Figure 2
Figure 3
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10. WITHDRAWAL PERIOD
Zero days.
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11. SPECIAL STORAGE CONDITIONS
Keep out of the sight and reach of children.
Lyophilisate : Store in a refrigerator (2 °C – 8 °C). Protect from light.
Solvent : This medicinal product does not require any special storage conditions.
Shelf life after reconstitution according to directions: 4 hours.
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12. SPECIAL WARNINGS
Special warnings:
Shedding of the vaccine strain from the injection site can be observed for a period of four days after vaccination.
From literature, it is known that a very low number of horses may develop purpura haemorrhagica if they are vaccinated shortly after infection. Purpura haemorrhagica has not been observed in any of the safety studies performed during development of Equilis StrepE. As the incidence of purpura haemorrhagica is very low, its occurrence cannot be ruled out completely.
In the challenge studies performed by the company, insufficient protection was seen in approximately one quarter of horses vaccinated with the recommended dose.
Do not use antibiotics within one week after vaccination.
The vaccine strain is sensitive to penicillins, tetracyclines, macrolides and lincomycin.
The vaccine strain is resistant to aminoglycosides, sulphonamides, flumequine and trimetroprim-sulfa combinations.
Special precautions for use in animals
Only healthy horses should be vaccinated.
Ensure that the lyophilisate is completely reconstituted before use.
Basic vaccination performed during an outbreak is not efficacious, because immunity is insufficient until basic vaccination has been completed.
Special precautions to be taken by the person administering the veterinary medicinal product to animals
To the user:
This product contains a live bacterial deletion mutant with a limited growth potential in mammalian tissue. Accidental self-injection may result in an inflammatory reaction with severe pain and swelling. Special care must be taken when connecting the applicator to the needle to avoid needle-stick injuries. In case of accidental self-injection, seek medical advice immediately and show the package insert or the label to the physician even if only a very small amount is injected.
To the physician:
This product contains a live auxotrophic deletion mutant Streptococcus equi vaccine strain with attenuated virulence. However, the bacterial compounds of this product can cause an inflammatory reaction with intense and painful swelling after accidental injection.
Anti-inflammatory therapy is indicated even if only a very small amount of the product in injected. An additional antibiotic treatment should be considered for safety reasons. The sensitivity of the vaccine strain to antibiotics is listed above.
Use during pregnancy, lactation or lay:
Do not use in pregnant or lactating mares.
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.
Overdose (symptoms, emergency procedures, antidotes):
In addition to the clinical signs given under section 6, vaccination with a ten times overdose may induce an abscess in one of the submandibular lymph nodes. The abscesses drain purulent material from 2 weeks after vaccination, but heal without intervention within a month thereafter. Furthermore, an increase in rectal temperature up to 2.5 °C may occur on the day of vaccination. Slight apathy may occasionally be observed one day after vaccination.
Incompatibilities:
Do not mix with any other veterinary medicinal products except the solvent supplied for use with the vaccine.
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13. SPECIAL PRECAUTIONS FOR THE DISPOSAL OF UNUSED PRODUCT OR WASTE MATERIAL, IF ANY
Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal product should be disposed of in accordance with local requirements.
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14. DATE ON WHICH THE PACKAGE LEAFLET WAS LAST REVISED
Detailed information on this veterinary medicinal product is available on the website of the European
Medicines Agency.
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15. OTHER INFORMATION