BANAMINE Solution

Country: Canada

Language: French

Source: Health Canada

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Active ingredient:

FLUNIXINE (MÉGLUMINE DE FLUNIXINE)

Available from:

INTERVET CANADA CORP

ATC code:

Sans

Dosage:

50MG

Pharmaceutical form:

Solution

Composition:

FLUNIXINE (MÉGLUMINE DE FLUNIXINE) 50MG

Administration route:

Intramusculaire

Units in package:

100ML/250ML

Prescription type:

Prescription

Therapeutic group:

Bétails; Porcs; Chevaux

Therapeutic area:

objet

Product summary:

Numéro de groupe d'ingrédients actifs (GIA) :0113433001

Authorization status:

APPROUVÉ

Authorization date:

2009-05-01

Patient Information leaflet

                                BANAMINE 250 ML ECL LABEL
Main panel (Base label and booklet first page)
PR BANAMINE®
FLUNIXIN MEGLUMINE INJECTABLE SOLUTION (MFR. STD.)
SOLUTION INJECTABLE DE FLUNIXINE MEGLUMINE (NORME DU FABR.)
VETERINARY USE ONLY/USAGE VETERINAIRE SEULEMENT
DIN 00465305
NET: 250 ML
STERILE / STERILE.
NONSTEROIDAL ANTI-INFLAMMATORY
ANTI-INFLAMMATOIRE NON STEROIDIEN
WARNINGS: TREATED ANIMALS MUST NOT BE SLAUGHTERED FOR USE IN FOOD FOR
AT LEAST 6 DAYS
FOR CATTLE AND 13 DAYS FOR SWINE AFTER THE LATEST TREATMENT WITH THIS
DRUG. MILK TAKEN FROM
TREATED ANIMALS DURING TREATMENT AND WITHIN 36 HOURS AFTER THE LATEST
TREATMENT MUST NOT
BE USED AS FOOD. NOT FOR USE IN VEAL CALVES. THIS DRUG IS NOT TO BE
ADMINISTERED TO HORSES
THAT ARE TO BE SLAUGHTERED FOR FOOD. KEEP OUT OF REACH OF CHILDREN.
MISES EN GARDE : LES ANIMAUX TRAITES NE DOIVENT PAS ETRE ABATTUS A DES
FINS
ALIMENTAIRES DANS UN DELAI D'AU MOINS 6 JOURS POUR LES BOVINS ET 13
JOURS POUR LES PORES
APRES LE DERNIER TRAITEMENT AVEC CE MEDICAMENT. LE LAIT PROVENANT DES
ANIMAUX TRAITES QUI
EST EXTRAIT PENDANT LE TRAITEMENT ET DANS LES 36 HEURES APRES
ADMINISTRATION DE LA DERNIERE
DOSE NE DOIT PAS ETRE UTILISE COMME ALIMENT. NE PAS UTILISER CHEZ LES
VEAUX DE LAIT. CE
MEDICAMENT NE DOIT PAS ETRE ADMINISTRE AUX CHEVAUX DEVANT ETRE ABATTUS
A DES FINS
ALIMENTAIRES. GARDER HORS DE LA PORT& DES ENFANTS.
MERCK LOGO
DESCRIPTION: EACH ML CONTAINS:
ACTIVE INGREDIENTS:
50 MG FLUNIXIN EQUIVALENT TO
83 MG FLUNIXIN MEGLUMINE.
DOSAGE
AND ADMINISTRATION:
DO NOT EXCEED THE RECOMMENDED DOSE.
HORSES:
1.1 MG FLUNIXIN PER KG (1 ML/ 45 KG) BODY WEIGHT ONCE DAILY. I.V. OR
I.M., AND REPEATED
FOR UP TO 5 DAYS FOR MUSCULOSKELETAL DISORDERS.
CATTLE:
2.2 MG FLUNIXIN PER KG (2 ML/ 45
KG) BODY WEIGHT BY SLOW I.V. ADMINISTRATION AS A SINGLE DOSE FOR ACUTE
BOVINE MASTITIS
AND ONCE A DAY FOR UP TO 3 DAYS FOR BRD AND ENDOTOXEMIA.
SWINE:
2.2 MG FLUNIXIN PER KG
(2 ML PER 45 KG) BODY WEIGHT GIVEN BY A SINGLE I.M ADMINISTRATION IN
THE NECK
MUSCULATURE ONLY. MAX 10 ML PER SITE.
SEE
PACKAGE INSERT FOR COMPLETE PRODUCT INFO
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet English 09-10-2008

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