PARAMECTIN 0.08 % W/V DRENCH FOR SHEEP

Ülke: İrlanda

Dil: İngilizce

Kaynak: HPRA (Health Products Regulatory Authority)

şimdi satın al

Indir Ürün özellikleri (SPC)
03-09-2015

Aktif bileşen:

IVERMECTIN

Mevcut itibaren:

Norbrook Laboratories Limited

ATC kodu:

QP54AA01

INN (International Adı):

IVERMECTIN

Doz:

0.8 %w/v

Farmasötik formu:

Oral Solution

Reçete türü:

LM-Licensed Merchant

Terapötik grubu:

Ovine

Terapötik alanı:

Ivermectin

Terapötik endikasyonlar:

Endoparasiticide

Yetkilendirme durumu:

Authorised

Yetkilendirme tarihi:

2001-01-12

Ürün özellikleri

                                SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Paramectin 0.08% w/v Drench for Sheep.
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each ml contains:
Active Ingredient
Ivermectin
0.8 mg
Excipient(s)
Benzyl alcohol (E1519)
0.03 ml
For a full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
Oral solution.
A clear yellow pale liquid.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Sheep.
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For the treatment of the following gastrointestinal nematodes, lungworms and nasal bots of sheep.
GASTROINTESTINAL ROUNDWORMS (ADULT AND FOURTH STAGE LARVAE):
_Haemonchus contortus_
[adult, L4 and inhibited L4],
_Ostertagia (Teladorsagia) circumcincta _[adult, L4 and inhibited L4]
_Trichostrongylus _spp
_Cooperia curticei _(adults)
_Cooperia oncophora _[adult and L4]
_Nematodirus _spp including _N. battus_
_Strongyloides papillosus_
_Oesophagostomum columbianum _[adult and L4]
_Oesophagostomum venulosum _(adults)
_Chabertia ovina _(adults)
LUNGWORMS (ADULT AND IMMATURE):
_Dictyocaulus filaria_
NASAL BOT (ALL LARVAL STAGES):
_Oestrus ovis_
HEALTH PRODUCTS REGULATORY AUTHORITY
________________________________________________________________________________________________________________________
_Date Printed 19/08/2015_
_CRN 7021379_
_page number: 1_
4.3 CONTRAINDICATIONS
Do not use in sheep known to be hypersensitive to ivermectin.
See section 4.7.
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.
•
Underdosing, which may be due to underestimation of body weight, misadministration of the product, or lack
                                
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