Zelys vet.

16 x 6 pc
Chewable tablet
PO

Active substance

  • Pimobendane : 5 mg
  • Species

    Dogs

    Indications

    For the treatment of canine congestive heart failure originating from valvular insufficiency (mitral and/or tricuspid valve regurgitation) or dilated cardiomyopathy. (See also section 4.9).

    Dose to be administered and administration route

    Do not exceed the recommended dosage.

    Determine the bodyweight accurately before treatment to ensure correct dosage. The tablets should be administered orally at a dose range of 0.2 mg to 0.6 mg pimobendan/kg body weight per day. The preferable daily dose is 0.5 mg pimobendan/kg body weight. The dose should be divided into two administrations (0.25 mg/kg body weight each), using a suitable combination of whole, or half of tablets. One half of the dose in the morning and the other half approximately 12 hours later.

    Each dose should be given approximately one hour before feeding. Spontaneous intake by the animal or place the tablet behind the lingual torus.

    This corresponds to:
    One 5 mg chewable tablet in the morning and one 5 mg chewable tablet in the evening for a body weight of 20 kg.

    Tablets are divisible in 2 for the 1.25, 5 and 10 mg tablet.
    The product may be combined with a diuretic treatment such as furosemide.

    Adverse reactions

    In rare cases a slight positively chronotropic effect (rise in heart rate) and vomiting can occur. However, these effects are dose-dependent and can be avoided by reducing the dose.

    In rare cases transient diarrhoea, anorexia or lethargy have been observed.

    Although a relationship with pimobendan has not been clearly established, in very rare cases, signs of effects on primary haemostasis (petechiae on mucous membranes, subcutaneous haemorrhages) may be observed during treatment. These signs disappear when the treatment is withdrawn. In rare cases, an increase in mitral valve regurgitation has been observed during chronic pimobendan treatment in dogs with mitral valve disease.

    The frequency of adverse reactions is defined using the following convention:

    - very common (more than 1 in 10 animals treated displaying adverse reactions(s))

    - 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).

    References

    Leaflet is unavailable
    Dog
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    Art. Nr. 15052/5052
    EAN 3411113046057
    PACKAGES
    Zelys vet.
    Ceva Animal Health
    16 x 6 pc
    15052/5052

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