FUROSORAL 40 MG TABLETS FOR CATS AND DOGS
Šalis: Airija
kalba: anglų
Šaltinis: HPRA (Health Products Regulatory Authority)
Prekės savybės
(SPC)
25-03-2015
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Veiklioji medžiaga:
FUROSEMIDE
Prieinama:
Le Vet Beheer B.V.
ATC kodas:
QC03CA01
INN (Tarptautinis Pavadinimas):
FUROSEMIDE
Dozė:
40 mg/tablet
Vaisto forma:
Tablets
Recepto tipas:
POM
Farmakoterapinė grupė:
Canine, Feline
Gydymo sritis:
Furosemide
Terapinės indikacijos:
Cardiovascular
Autorizacija statusas:
Authorised
Leidimo data:
2015-02-20
Prekės savybės
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Furosoral 40 mg tablets for cats and dogs
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
1 tablet contains:
ACTIVE SUBSTANCE:
Furosemide 40 mg
For the full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
Tablet.
White to yellow-white round and convex tablet with a cross-shaped break line on one side. Tablets can be divided into
two or four equal parts.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Cats and dogs.
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
Treatment of hydrothorax, hydropericardium, ascites and oedema, particularly associated with cardiac insufficiency and
renal dysfunction.
4.3 CONTRAINDICATIONS
Do not use in animals suffering from hypovolaemia, hypotension or dehydration.
Do not use in cases of renal failure with anuria.
Do not use in cases of electrolyte deficiency.
Do not use in cases of known hypersensitivity to furosemide, sulphonamides or any of the excipients.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
Therapeutic efficacy may be impaired by increased intake of drinking water. Where the animal’s condition permits,
water intake should be restricted to physiologically normal levels during treatment.
HEALTH PRODUCTS REGULATORY AUTHORITY
________________________________________________________________________________________________________________________
_Date Printed 10/03/2015_
_CRN 7019898_
_page number: 1_
4.5 SPECIAL PRECAUTIONS FOR USE
SPECIAL PRECAUTIONS FOR USE IN ANIMALS
Furosemide should be used with caution in the case of pre-existing electrolyte and/or water imbalance, impaired
hepatic function (may precipitate hepatic coma) and diabetes mellitus.
In case of prolonged treatment, hydration status and serum electrolytes should be monitored frequently.
1-2 days before and after commenc
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