Noroclav
Active substance
ATC code
Species
Cattle and Dogs.
Indications
Noroclav Injection has a broad-spectrum of bactericidal activity against the bacteria commonly found in cattle and dogs.
(a) In vitro Noroclav Injection is active against a wide range of clinically important bacteria including:
Gram-positive: Staphylococci (including beta-lactamase producing strains), Streptococci, Corynebacteria, Clostridia, Bacillus anthracis, Actinomyces bovis.
Gram-negative: Escherichia coli (including beta-lactamase producing strains), Salmonella spp (including beta-lactamase producing strains), Campylobacter spp, Klebsiella spp, Proteus spp, Pasteurellae spp, Fusobacterium necrophorum, Bacteroides (including beta-lactamase producing strains), Haemophilus spp, Moraxella spp and
Actinobacillus lignieresi.
(b) Noroclav Injection is indicated for the treatment of diseases including:
Cattle:
Respiratory infections
Soft tissue infections (e.g. joint/navel ill, abscesses etc.)
Metritis
Mastitis.
Dogs:
Respiratory tract infections
Urinary tract infections
Skin and soft tissue infections (e.g. abscesses, pyoderma, anal sacculitis and gingivitis.)
Dose to be administered and administration route
The product is indicated for intramuscular administration to cattle and subcutaneous administration to dogs.
The recommended dosage rate is 8.75 mg/kg bodyweight (1 ml per 20 kg bodyweight) daily for 3-5 days. Shake the vial well before use. After injection, massage the injection site. This product does not contain an antimicrobial preservative. Use a completely dry sterile needle and syringe.
Swab the septum before removing each dose.
Care should be taken to avoid contaminating the remaining contents of a vial with water. Clavulanic acid is moisture sensitive. It is very important therefore, that a completely dry needle and syringe is used when extracting suspension for injection in order to avoid contaminating the remaining contents of the vial with drops of water. Contamination will result in obvious beads of dark, brown discolouration corresponding to the introduced water droplets. Material affected in this way should not be used as it may have significantly reduced potency.
Adverse reactions
Use of the product may occasionally result in pain on injection and/or local tissue reaction.
References
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Art. Nr. | |
EAN | 5023534002987 |