Medine.co.uk

Eurican L

Revised: May 2012

AN: 02065/2011



SUMMARY OF PRODUCT CHARACTISTICS





1.

NAME OF THE VETERINARY MEDICINAL PRODUCT




EURICAN L



2.

QUALITATIVE AND QUANTITATIVE COMPOSITION




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



3.

PHARMACEUTICAL FORM




Suspension for injection.



4.

CLINICAL PARTICULARS



4.1

Target species




Dogs from 8 weeks of age.



4.2

Indications for use specifying the target species




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.



4.3

Contra-indications




None



4.4

Special warnings for each target species




None.



4.5

Special precautions for use, including special precautions to be taken by the person administering the medicinal product to animals




Special precautions for use in animals




Vaccinate only healthy animals.





ii. Special precautions to be taken by the person administering the medicinal product to the animals




In the case of accidental self-injection, wash the area immediately with water.



4.6

Adverse reactions (frequency and seriousness)




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.



4.7

Use during pregnancy, lactation or lay




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.



4.8

Interaction with other medicinal products and other forms of interaction




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.



4.9

Amounts to be administered and administration route




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.



4.10

Overdose (symptoms, emergency procedures, antidotes), if necessary




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.



4.11

Withdrawal periods




Not applicable




5.


IMMUNOLOGICAL PROPERTIES




The vaccine stimulates active immunity against Leptospira canicola and Leptospira icterohaemorrhagiae leptospiroses.




ATC Vet Code: QI07AB01

6.

PHARMACEUTICAL PARTICULARS



6.1

List of excipients




Phosphate buffered saline.



6.2

Major incompatibilities




Do not mix with any other veterinary medicinal product except Eurican DHPPi and Eurican P.



6.3

Shelf-life




Shelf-life of the veterinary medicinal product as packaged for sale: 2 years.



6.4

Special precautions for storage




Store and transport at 2ºC – 8ºC (in a refrigerator), protected from light.



6.5

Nature and composition of immediate packaging




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




Any unused veterinary medicinal product or waste material derived from such veterinary medicinal products should be disposed of in accordance with local requirements.



7

MARKETING AUTHORISATION HOLDER




Merial Animal Health Limited

PO Box 327

Sandringham House

Harlow Business Park

Harlow

Essex

CM19 5TG



8.

MARKETING AUTHORISATION NUMBER(S)




UK: Vm 08327/4148

IE: VPA 10857/55/1



9.

DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION




Date: UK: 28th October 2005

Date: IE: 5th November 2004



10.

DATE OF REVISION OF THE TEXT




Date: May 2012




PROHIBITION OF SALE, SUPPLY AND/OR USE




Not applicable


Page 4 of 4