Endofluke 100 mg/ml Oral Suspension

Šalis: Airija

kalba: anglų

Šaltinis: HPRA (Health Products Regulatory Authority)

Veiklioji medžiaga:

Triclabendazole

Prieinama:

Cross Vetpharm Group Limited

ATC kodas:

QP52AC01

INN (Tarptautinis Pavadinimas):

Triclabendazole

Dozė:

100 milligram(s)/millilitre

Vaisto forma:

Oral suspension

Recepto tipas:

LM: Licensed Merchant as defined in relevant national legislation

Farmakoterapinė grupė:

Cattle, Sheep

Gydymo sritis:

triclabendazole

Terapinės indikacijos:

Endoparasiticide

Autorizacija statusas:

Authorised

Leidimo data:

2002-08-01

Prekės savybės

Health Products Regulatory Authority
03 May 2019
CRN0091QM
Page 1 of 5
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Endofluke 100 mg/ml Oral Suspension
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Active Substance per ml
Triclabendazole 100 mg
Excipients
Methyl Parahydroxybenzoate (E218) 2 mg (preservative)
Propyl Parahydroxybenzoate (E216) 0.2 mg (preservative)
For a full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
Oral Suspension.
A white to off-white suspension.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Cattle & Sheep
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For the treatment of adult, immature and early immature stages of
liver fluke (_Fasciola hepatica_) susceptible to triclabendazole.
4.3 CONTRAINDICATIONS
Do not use in animals known to be hypersensitive to the active
substance.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
Care should be taken to avoid the following practices, because they
increase the risk of development of resistance and could
ultimately result in ineffective therapy:
- Too frequent and repeated use of anthelmintics from the same class,
over an extended period of time.
- Under dosing, which may be due to under estimation of bodyweight,
misadministration of the product or lack of calibration
of the dosing device (if any).
Suspected clinical cases of resistance to anthelmintics should be
further investigated using appropriate tests (e.g. Faecal Egg
Count Reduction Test). Where the results of the test(s) strongly
suggest resistance to a particular anthelmintic, an anthelmintic
belonging to another pharmacological class and having a different mode
of action should be used.
Resistance to triclabendazole has been reported in _Fasciola hepatica
_in cattle and sheep. Therefore, the use of this product
should be based on local (regional/farm) epidemiological information
about susceptibility of the _Fasciola hepatica _and
recommendations on how to limit further selection for resistance to
anthelmintics.
Health Products Regulatory Authority