CARPRIEVE 50 MG/ML SOLUTION FOR INJECTION FOR CATTLE
Land: Irland
Språk: engelsk
Kilde: HPRA (Health Products Regulatory Authority)
Preparatomtale
(SPC)
27-04-2024
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Aktiv ingrediens:
CARPROFEN
Tilgjengelig fra:
Norbrook Laboratories Limited
ATC-kode:
QM01AE91
INN (International Name):
CARPROFEN
Dosering :
50 Mg/Ml
Legemiddelform:
Solution for Injection
Resept typen:
POM
Terapeutisk gruppe:
Bovine
Terapeutisk område:
Carprofen
Indikasjoner:
N.S.A.I.D
Autorisasjon status:
Authorised
Autorisasjon dato:
2007-05-04
Preparatomtale
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Carprieve 50 mg/ml Solution for Injection for Cattle.
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each ml contains:
ACTIVE SUBSTANCE:
Carprofen
50 mg
EXCIPIENTS:
Ethanol (anhydrous)
100 mg
Sodium Formaldehyde Sulphoxylate
2 mg
For a full list of excipients, see section 6.1
3 PHARMACEUTICAL FORM
Solution for Injection.
A clear colourless to pale yellow solution.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Cattle.
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
The product is indicated as an adjunct to antimicrobial therapy to reduce pyrexia in acute cases of infectious respiratory
disease in cattle.
4.3 CONTRAINDICATIONS
Do not use in animals suffering from cardiac, hepatic or renal impairment.
Do not use in animals suffering from gastrointestinal ulceration or bleeding.
Do not use where there is evidence of a blood dyscrasia.
Do not use in animals with known hypersensitivity to the product.
For use in pregnant animals refer to section 4.7.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
None.
IRISH MEDICINES BOARD
________________________________________________________________________________________________________________________
_Date Printed 31/10/2012_
_CRN 7012931_
_page number: 1_
4.5 SPECIAL PRECAUTIONS FOR USE
SPECIAL PRECAUTIONS FOR USE IN ANIMALS
Do not exceed the stated dose or the duration of treatment.
Do not administer other NSAIDs concurrently or within 24 hours of each other. Some NSAIDs may be highly bound
to plasma proteins and compete with other highly bound drugs, which can lead to toxic effects.
Use in any animal less than 6 weeks of age, or in aged animals, may involve additional risk. If such use cannot be
avoided animals may require a reduced dosage and careful clinical management.
Avoid use in
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