Alonate-P 400 mg/g Oral Paste for Horses and Ponies

Ülke: Birleşik Krallık

Dil: İngilizce

Kaynak: VMD (Veterinary Medicines Directorate)

şimdi satın al

Ürün özellikleri Ürün özellikleri (SPC)
23-05-2018

Aktif bileşen:

Pyrantel Embonate

Mevcut itibaren:

Cross Vetpharm Group Ltd

ATC kodu:

QP52AF02

INN (International Adı):

Pyrantel Embonate

Farmasötik formu:

Oral paste

Reçete türü:

POM-VPS -Prescription Only Medicine – Veterinarian, Pharmacist, Suitably Qualified Person

Terapötik grubu:

Horses

Terapötik alanı:

Anthelmintic

Yetkilendirme durumu:

Authorized

Yetkilendirme tarihi:

2015-03-27

Ürün özellikleri

                                AN: 00498/2014
Issued: March 2015
SUMMARY OF PRODUCT CHARACTERISTICS
1.
NAME OF VETERINARY MEDICINAL PRODUCT
Alonate-P 400 mg/g Oral Paste for Horses and Ponies
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Active Substance
mg/g
Pyrantel embonate
400 mg/g
Excipients
Butylated Hydroxytoluene
0.2 mg/g
For full list of excipients, please see section 6.1.
3.
PHARMACEUTICAL FORM
Oral Paste
Pale yellow to buff coloured paste
4.
CLINICAL PARTICULARS
4.2
TARGET SPECIES
Horses and ponies.
4.3
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
Pyrantel embonate is a broad spectrum anthelmintic. Pyrantel embonate
is
indicated for use in the horse for the control and treatment of adult
infections
of large and small strongyles, Pinworms, Roundworms, Tapeworms.
Pyrantel embonate has a broad spectrum of activity, including activity
against:
Large strongyles:
_Stronglylus vulgaris, S. edentatus, S. equinus._
Small strongyles:
_Trichonema spp. (Cyathostomes), Triodontophorus spp._
Pinworms:
_Oxyuris equi, Probstmayria vivipara._
Large roundworms:
_Parascaris equorum._
Tape worms:
_Anoplocephala perfoliata._
4.4
CONTRA-INDICATIONS
Not for use in foals less than 4 weeks of age.
Contraindicated in known sensitivity to pyrantel and in severely
debilitated
animals.
Page 1 of 6
AN: 00498/2014
Issued: March 2015
4.5
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.

Underdosing, which may be due to underestimation of weight,
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 a
                                
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