Libeo 10 mg Chewable Tablets for Dogs
Active ingredient: Furosemide
Form
Chewable
Species
Manufacturer
Ceva Sante Animale
VMD MA No.
14966/5041
What it's used for
associated with cardiac insufficiency, renal dysfunction, trauma and parasitic disease. It is also recommended for the treatment of mammary oedema and limb...
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Prescription required
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Libeo 10 mg Chewable Tablets for Dogs — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.
is also recommended for the treatment of mammary oedema and limb oedemata.
The veterinary medicinal product gives rapid onset of diuretic action with increased
sodium and water excretion. It is even effective where glomerular filtration is impaired.
SpeciesDosage mg active/kg
bodyweight
ml of 50 mg/ml
solution
AdministrationHorse0.5 – 1.0 IV1 – 2 ml per 100 kg1 – 2 times/day
at intervals of
6 – 8 hours
Cattle0.5 – 1.0 IV1 – 2 ml per 100 kgAt intervals of
12 – 14 hours
Dog/cat2.5 – 5.0 IM/IV0.25 – 0.5 (per 5 kg
bodyweight)
First dose
5 mg/kg
reduced to
1 – 2 mg/kg for
maintenance at
6 – 8 hour
intervals.
In severe or refractory cases, the dose may be doubled on a single occasion in the
horse or cow.
The veterinary medicinal product may be administered observing aseptic precautions:
Onset and Duration of Action
SpeciesRouteTime of onsetDurationDogIV or IMAfter 10 – 15 minutes2 – 3 hours
deficiency disease or overdosage with digitalis.
Do not use concurrently with aminoglycoside antibiotic treatment.
The therapeutic effect may be impaired by increased intake of drinking water. So far as
the patient's condition allows, the amount of drinking water should be restricted.
Do not use in cases of hypersensitivity to the active substance or to any of the
excipients.
Very rare
(<1 animal / 10,000 animals
treated, including isolated
reports):
Haemoconcentration; Circulatory Impairment;
Hypokalaemia
, Hyponatraemia
;
In case of longer therapy.
Dogs:
Very rare
(<1 animal / 10,000 animals
treated, including isolated
reports):
Haemoconcentration; Circulatory Impairment;
Hypokalaemia
, Hyponatraemia
;
Vomiting
; Staggering
1
In case of longer therapy.
Following too rapid injection.
Reporting adverse events is important. It allows continuous safety monitoring of a
veterinary medicinal product. Reports should be sent, preferably via a veterinarian, to
either the marketing authorisation holder or its local representative or the national
competent authority via the national reporting system. See the package leaflet for
respective contact details.
Special precautions for safe use in the target species:
Clinical experience with dogs indicates that improved results can frequently be achieved
by supplementary administration of corticosteroids.
In pulmonary oedema of cardiac origin, combined therapy with cardiac glycosides is
advisable. Only during prolonged treatment is it necessary to monitor potassium
balance. Potassium supplements may be necessary.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals:
Care should be taken to avoid accidental self-injection. If irritation occurs, seek medical
advice and show the package leaflet or the label to the physician.
Following skin/eye contamination, wash/irrigate area with clean, running water
immediately.
Wash hands after use.
Special precautions for the protection of the environment:
Not applicable.
nephrotoxicity with cephalosporins.
Use in combination with sulphonamide treatment may lead to sulphonamide allergy.
Keep the container in the outer carton in order to protect from light.
If the product is stored for a prolonged period below 18 °C, crystalline precipitation may
occur. Do not use the product whilst these crystals are present. The crystals may be
redissolved by shaking the vial and then storing it for 24 hours at 30 °C - 40 °C. Once
the crystals are redissolved, the product may be used.
Discard unused material.
Meat and offal: 28 days.
Milk: 24 hours.
Horses:
Not to be used in horses intended for human consumption.
Treated horses may never be slaughtered for human consumption.
The horse must have been declared as not intended for human consumption under
national horse passport legislation.
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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Other Products Containing Furosemide
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
Dimazon 50 mg/ml Solution for Injection for Cattle, Horses, Cats and Dogs
POM-VIntervet International B.V.
Fumexx 50 mg/ml Solution for Injection for Cattle, Horses, Dogs and Cats
POM-VAlfasan Nederland B.V.
Furosemide Tablets BP (Vet) 20 mg
POM-VMillpledge Europe BV
Furosemide Tablets BP (Vet) 20 mg
POM-VMillpledge Europe BV
Furosemide Tablets BP (Vet) 40 mg
POM-VMillpledge Europe BV
Furosemide Tablets BP (Vet) 40 mg
POM-VMillpledge Europe BV
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