Parazole 10% w/v Oral Suspension

Država: Irska

Jezik: angleščina

Source: HPRA (Health Products Regulatory Authority)

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Lastnosti izdelka Lastnosti izdelka (SPC)
12-06-2017
Javno poročilo o oceni Javno poročilo o oceni (PAR)
12-06-2017
DSU DSU (DSU)
17-03-2023

Aktivna sestavina:

Fenbendazole

Dostopno od:

Foran Healthcare Limited

Koda artikla:

QP52AC13

INN (mednarodno ime):

Fenbendazole

Odmerek:

10 percent weight/volume

Farmacevtska oblika:

Oral suspension

Tip zastaranja:

CAM: Companion Animal Medicine as defined in relevant national legislation

Terapevtska skupina:

Cats, Dogs

Terapevtsko območje:

fenbendazole

Terapevtske indikacije:

Endoparasiticide

Status dovoljenje:

Authorised

Datum dovoljenje:

1997-10-01

Lastnosti izdelka

                                SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Parazole 10% w/v Oral Suspension
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
3 PHARMACEUTICAL FORM
Oral suspension.
A white to off-white suspension.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Dogs and cats
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
A broad spectrum anthelmintic for the treatment of domestic dogs and
cats infected with immature and mature stages of
nematodes of the gastrointestinal and respiratory tracts.
Effective against immature and mature ascarids, hookworms and
tapeworms. Also kills roundworm eggs.
4.3 CONTRAINDICATIONS
Do not use in case of known hypersensitivity to the active substance
or to any of the excipients.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
None known.
4.5 SPECIAL PRECAUTIONS FOR USE
Special precautions for use in animals:
Ensure correct weight estimation and dose calculation.
Special precautions to be taken by the person administering the
product to animals:
Avoid contact with the product.
Wash hands after use.
4.6 ADVERSE REACTIONS (FREQUENCY AND SERIOUSNESS)
None known .
Each ml contains:
Active substance
Fenbendazole
100 mg
Excipients
Methyl Parahydroxybenzoate
2.5 mg
For the full list of excipients, see section 6.1.
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4.7 USE DURING PREGNANCY, LACTATION OR LAY
Pregnan
                                
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