SUMEX 1% W/V, SOLUTION FOR INJECTION FOR CATTLE
Country: Ireland
Language: English
Source: HPRA (Health Products Regulatory Authority)
Summary of Product characteristics
(SPC)
07-01-2016
Some documents for this product are not currently available, you can send a request to our customer service and we will notify you as soon as we are able to obtain them.
Send request.
Send request.
Active ingredient:
IVERMECTIN
Available from:
Chanelle Animal Health Ltd.
ATC code:
QP54AA01
INN (International Name):
IVERMECTIN
Dosage:
1.0 %w/v
Pharmaceutical form:
Solution for Injection
Prescription type:
LM-Licensed Merchant
Therapeutic group:
Bovine
Therapeutic area:
Ivermectin
Therapeutic indications:
Endectoparasiticides
Authorization status:
Authorised
Authorization date:
2002-06-28
Summary of Product characteristics
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Sumex 1% w/v, solution for injection for cattle
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Active Substance
Ivermectin
1.0 % w/v (10 mg/ml)
For a full list of excipients, see section 6.1
3 PHARMACEUTICAL FORM
Solution for injection
Clear, colourless to slightly yellow solution
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Cattle (Beef and non lactating cattle)
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
The product is indicated for the effective treatment of the following harmful parasites of cattle:
GASTRO-INTESTINAL ROUNDWORMS:
_Ostertagia _spp (including inhibited _O. ostertagi (adult and L4_)),
_Haemonchus placei (adult and L4_),
_Trichostrongylus spp (adult and L4_),
_Cooperia _spp _(adult and L4_),
_Nematodirus spp (adult_),
LUNGWORMS (adult and fourth stage larvae):
_Dictyocaulus viviparus_
WARBLES (parasitic stages):
_Hypoderma spp_
MANGE MITES:
_Psoroptes bovis_
_Sarcoptes scabiei _var. _bovis_.
SUCKING LICE:
_Linognathus vituli_,
_Haematopinus eurysternus_
PERSISTENT ACTIVITY
Treatment at the recommended dose rate controls re-infection with _Haemonchus placei _and _Cooperia spp. _acquired up
HEALTH PRODUCTS REGULATORY AUTHORITY
________________________________________________________________________________________________________________________
_Date Printed 23/12/2015_
_CRN 7022491_
_page number: 1_
to 14 days after treatment, _Ostertagia ostertagi _acquired up to 21 days after treatment and _Dictyocaulus viviparus_
acquired up to 28 days after treatment.
To obtain maximum benefit from the persistent activity of the product for grazing animals it is recommended that
calves which are set-stocked in their first grazing season should be treated 3, 8 and 13 weeks after the day of turn-out.
This can protect the animals from parasit
Read the complete document
