Eurican L
Revised: May 2012
AN: 02065/2011
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SUMMARY OF PRODUCT CHARACTISTICS |
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1. |
NAME OF THE VETERINARY MEDICINAL PRODUCT |
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EURICAN L |
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2. |
QUALITATIVE AND QUANTITATIVE COMPOSITION |
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Inactivated Leptospira canicola } > 80% protection* Inactivated Leptospira icterohaemorrhagiae } Excipient……………………………………………………………q.s. 1 dose of 1ml *According to Ph. Eur. hamster potency test For a full list of excipients, see section 6.1 |
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3. |
PHARMACEUTICAL FORM |
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Suspension for injection. |
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4. |
CLINICAL PARTICULARS |
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4.1 |
Target species |
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Dogs from 8 weeks of age. |
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4.2 |
Indications for use specifying the target species |
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In dogs: Active immunisation against Leptospira canicola and Leptospira icterohaemorrhagiae to prevent mortality and to reduce clinical symptoms of Leptospira infections caused by these agents. Onset of immunity: 14 days after primary vaccination. The duration of immunity is one year. |
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4.3 |
Contra-indications |
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None |
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4.4 |
Special warnings for each target species |
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None. |
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4.5 |
Special precautions for use, including special precautions to be taken by the person administering the medicinal product to animals |
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Special precautions for use in animals |
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Vaccinate only healthy animals. |
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ii. Special precautions to be taken by the person administering the medicinal product to the animals |
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In the case of accidental self-injection, wash the area immediately with water. |
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4.6 |
Adverse reactions (frequency and seriousness) |
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In rare cases, immediately after injection, transient pain may occur at the injection site. A temperature increase of approximately 1°C lasting no more than a day may occur in rare cases. In rare circumstances a hypersensitivity reaction may occur, which may require appropriate symptomatic treatment. |
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4.7 |
Use during pregnancy, lactation or lay |
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In the absence of data from studies in seronegative bitches, the vaccine should only be used in pregnant bitches which have been vaccinated before pregnancy. |
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4.8 |
Interaction with other medicinal products and other forms of interaction |
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Safety and efficacy data are available which demonstrate that this vaccine can be used as a diluent for Eurican P or Eurican DHPPi. 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. 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. |
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4.9 |
Amounts to be administered and administration route |
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Inject by subcutaneous route a 1-ml dose according to the following schedule: Basic vaccination 1st injection: from 8 weeks of age. 2nd injection: 3 to 5 weeks later, from 12 weeks of age. Revaccination Annual boosters by administration of a single 1 ml dose. |
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4.10 |
Overdose (symptoms, emergency procedures, antidotes), if necessary |
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No adverse events, other than those reported in Section 4.6 for a single dose, were reported following administration of an overdose of the vaccine, except transitory and slight swelling at the injection site. |
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4.11 |
Withdrawal periods |
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Not applicable |
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5. |
IMMUNOLOGICAL PROPERTIES |
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The vaccine stimulates active immunity against Leptospira canicola and Leptospira icterohaemorrhagiae leptospiroses. |
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ATC Vet Code: QI07AB01 |
6. |
PHARMACEUTICAL PARTICULARS |
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6.1 |
List of excipients |
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Phosphate buffered saline. |
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6.2 |
Major incompatibilities |
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Do not mix with any other veterinary medicinal product except Eurican DHPPi and Eurican P. |
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6.3 |
Shelf-life |
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Shelf-life of the veterinary medicinal product as packaged for sale: 2 years. |
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6.4 |
Special precautions for storage |
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Store and transport at 2ºC – 8ºC (in a refrigerator), protected from light. |
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6.5 |
Nature and composition of immediate packaging |
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Type 1 glass bottle Butyl elastomer closure Bottle (glass) of 1 dose of suspension, box of 10 bottles Bottle (glass) of 1 dose of suspension, box of 50 bottles Not all pack sizes may be marketed. |
6.6 |
Special precautions for the disposal of unused veterinary medicinal product or waste materials derived from the use of such products |
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Any unused veterinary medicinal product or waste material derived from such veterinary medicinal products should be disposed of in accordance with local requirements. |
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7 |
MARKETING AUTHORISATION HOLDER |
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Merial Animal Health Limited PO Box 327 Sandringham House Harlow Business Park Harlow Essex CM19 5TG |
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8. |
MARKETING AUTHORISATION NUMBER(S) |
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UK: Vm 08327/4148 IE: VPA 10857/55/1 |
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9. |
DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION |
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Date: UK: 28th October 2005 Date: IE: 5th November 2004 |
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10. |
DATE OF REVISION OF THE TEXT |
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Date: May 2012 |
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PROHIBITION OF SALE, SUPPLY AND/OR USE |
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Not applicable |
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