Ecomectin 18.7 mg/g Oral Paste for Horses

País: Irlanda

Idioma: inglés

Fuente: HPRA (Health Products Regulatory Authority)

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Ficha técnica Ficha técnica (SPC)
22-03-2019
DSU DSU (DSU)
18-10-2023

Ingredientes activos:

Ivermectin

Disponible desde:

ECO Animal Health Europe Limited

Código ATC:

QP54AA01

Designación común internacional (DCI):

Ivermectin

Dosis:

18.7 milligram(s)/gram

formulario farmacéutico:

Oral paste

tipo de receta:

POM: Prescription Only Medicine as defined in relevant national legislation

Área terapéutica:

ivermectin

Estado de Autorización:

Authorised

Fecha de autorización:

2007-01-05

Ficha técnica

                                Health Products Regulatory Authority
21 March 2019
CRN008Y4J
Page 1 of 4
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Ecomectin 18.7 mg/g Oral Paste for Horses
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
ACTIVE SUBSTANCE:
​
​
Ivermectin
18.7
mg/g
​
​
​
EXCIPIENT(S):
​
​
For a full list of excipients, see section 6.1
3 PHARMACEUTICAL FORM
Oral Paste
A white homogeneous paste
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Horses
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
Treatment of nematode or arthropod infections due to:
Large strongyles:
_Strongylus vulgaris_ (adults and L
4
stage larvae [arterial])
_Strongylus edentatus_ (adults and L
4
stage larvae [tissue])
_Strongylus equinus_ (adults)
Small strongyles (including benzimidazole resistant strains):
_Cyathostomum spp _(adults and luminal L
4
stage larvae)
_Cylicocyclus spp_. (adults and luminal L
4
stage larvae)
_Cylicodontophorus spp_. (adults and luminal L
4
stage larvae)
_Cylicostephanus spp_. (adults and luminal L
4
stage larvae)
_Gyalocephalus spp_. (adults and luminal L
4
stage larvae)
Ascarids:
_Parascaris equorum_ (luminal L5 larvae and adults)
Pinworms:
_Oxyuris equi_ (L
4
stage larvae and adults)
Neck threadworms:
_Onchocerca spp._ (microfilariae)
Stomach bots:
_Gasterophilus spp. _(oral and gastric stages)
4.3 CONTRAINDICATIONS
Do not use in cases of hypersensitivity to the active substance or to
any of the excipients.
Do not use in dogs or cats as severe adverse reactions may occur.
Health Products Regulatory Authority
21 March 2019
CRN008Y4J
Page 2 of 4
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
Some horses with heavy infections of _Onchocerca_ spp. microfilariae
have experienced oedema and pruritus following treatment,
such reactions are assumed to be the result of death of large numbers
of microfilariae. These signs resolve within a few days
but symptomatic treatment may be advisable
Care shold be taken to avoid the following practices because they
increase the risk of development of resista
                                
                                Leer el documento completo
                                
                            

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