Eurican Lmulti Suspension for Injection
Active ingredients: Leptospira canicola, Leptospira grippotyphosa, Leptospira icterohaemorrhagiae
Form
Injection
Species
Manufacturer
Boehringer Ingelheim Vetmedica GmbH
VMD MA No.
04491/3015
What it's used for
Active immunisation of dogs to: - renal lesions caused by interrogans serogroup Icterohaemorrhagiae serovar Icterohaemorrhagiae - carriage and renal lesion...
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1
Ask your vet for a written prescription
They must provide one on request. Under the CMA Order the fee is capped at £21 from 2027.
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2
Fill it at a registered online retailer
The CMA found online pharmacies 50–60% cheaper than practice dispensing on common medicines — typically £200–£300 a year.
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Prescription required
Your vet must provide a written prescription on request. You can then purchase from any licensed online retailer.
Eurican Lmulti Suspension for Injection — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 26 Mar 2026.
-
renal lesions caused by interrogans serogroup Icterohaemorrhagiae
serovar Icterohaemorrhagiae
-
carriage and renal lesions caused by interrogans serogroup Canicola
serovar Canicola.
Revised: July 2025
AN: 00736/2025
-
carriage and renal lesions caused by kirschneri serogroup Grippotyphosa
serovar Grippotyphosa.
-
carriage and renal lesions caused by serogroup
Icterohaemorrhagiae serovar Copenhageni.**
Onset of immunity: 2 weeks after the second injection of the primary vaccination
course for all strains.
Duration of immunity: at least one year after the second injection of the primary
vaccination course for all strains.
* For
experiment for duration of immunity.
** For Leptospira Copenhageni the duration of immunity was not established.
When Eurican Lmulti is used as a diluent of a Boehringer Ingelheim freeze-dried
vaccine against distemper, adenovirosis, parvovirosis and parainfluenza type 2,
aseptically reconstitute the contents of the lyophilisate with the suspension for
injection. Shake well before use. The entire contents of the reconstituted vial should
be administered as a single dose.
The following schedule should be followed:
Primary vaccination:
weeks of age.
Revaccination:
vaccination course. Dogs should be revaccinated with a single booster dose on an
annual basis.
injection. It usually regresses within 1-6 days. This can, on some occasions, be
accompanied by slight pruritus, heat and pain at the injection site. Transient lethargy
and emesis may also commonly be observed.
Anorexia, polydipsia, hyperthermia, diarrhoea, muscle tremor, muscle weakness and
injection site cutaneous lesions may uncommonly be observed.
Hypersensitivity reactions (facial oedema, anaphylactic shock, urticaria) may rarely
occur, some of which are life-threatening. Appropriate symptomatic treatment should
promptly be provided.
The frequency of adverse reactions is defined using the following convention:
- very common (more than 1 in 10 animals treated displaying adverse reaction(s))
Revised: July 2025
AN: 00736/2025
- common (more than 1 but less than 10 animals in 100 animals treated)
- uncommon (more than 1 but less than 10 animals in 1,000 animals treated)
- rare (more than 1 but less than 10 animals in 10,000 animals treated)
- very rare (less than 1 animal in 10,000 animals treated, including isolated
reports).
Special precautions for use in animals
Apply usual aseptic procedures.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals
In case of accidental self-injection, seek medical advice immediately and show the
package leaflet or the label to the physician.
against distemper, adenovirosis, parvovirosis and parainfluenza type 2 respiratory
infections.
Safety and efficacy data are available which demonstrate that this vaccine can be
administered on the same day but not mixed with Boehringer Ingelheim's rabies
vaccine in dogs from 12 weeks of age. In that case, the efficacy against
Icterohaemorrhagiae was demonstrated only for the reduction of renal lesions and
bacterial excretion, and the efficacy against Grippotyphosa was
demonstrated only for the reduction of renal carriage, renal lesions and bacterial
excretion. Efficacy of the vaccine for protection against the Copenhageni serovar has
not been investigated after use with Boehringer Ingelheim’s rabies vaccine on the
same day.
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
Do not freeze.
Protect from light.
5. IMMUNOLOGICAL PROPERTIES
Pharmacotherapeutic group: Immunologicals for Canidae, Inactivated bacterial
vaccines for dogs.
ATCvet code: QI07AB01.
Vaccine against Leptospira (inactivated) in dogs.
After administration, the vaccine induces an immune response against
interrogans
Icterohaemorrhagiae,
kirschneri serogroup Grippotyphosa leptospirosis in the dog demonstrated by
challenge.
This information is sourced from the official Summary of Product Characteristics (SPC) published by the Veterinary Medicines Directorate (VMD). It is provided for informational purposes only and does not replace professional veterinary advice. Always consult your vet before administering any medication.
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Related Conditions
Other Products Containing Leptospira canicola
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
Canigen L4, Suspension for Injection for Dogs
POM-VIntervet International B.V.
Canigen Lepto 4, Suspension for Injection for Dogs
POM-VMSD Animal Health UK Limited
Canixin DHPPi/L
POM-VVIRBAC
CANIXIN DHPPi/L Lyophilisate and Suspension for Suspension for Injection for Dogs
POM-VVirbac
Canixin L Suspension for Injection for Dogs
POM-VVirbac
Canixin L Suspension for Injection for Dogs
POM-VVirbac
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