Presentation Synulox Ready-To-Use:
Suspension for Injection is an off-white suspension containing 35 mg/ml clavulanic acid as Potassium clavulanate and 140 mg/ml amoxicillin as Amoxicillin trihydrate.
Uses Synulox Ready-To-Use Suspension for Injection has a notably broad spectrum of bactericidal activity against the bacteria commonly found in cattle, pigs and small animals.
In vitro Synulox 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, Peptostreptococcus spp. Gram-negative: Actinobacillus pleuropneumoniae, Escherichia coli (including beta-lactamase producing strains),Salmonellae (including beta-lactamase producing strains), Bordetella bronchiseptica, Campylobacter spp., Klebsiellae, Proteus spp., Pasteurellae, Fusobacterium necrophorum, Bacteroides (including beta-lactamase producing strains), Haemophilus spp., Moraxella spp. and Actinobacillus lignieresi.
Clinically, Synulox has been shown to be effective in treating a wide range of diseases including:
Cattle: -Respiratory infections -Soft tissue infections (e.g. joint/navel ill, abscesses etc.) -Metritis -Mastitis
Pigs: -Respiratory bacterial infections in growing pigs -Colibacillosis -Periparturient infections in sows (eg mastitis, metritis and agalactia.)
Dogs and cats: -Respiratory tract infections -Urinary tract infections -Skin and soft tissue infections (e.g. abscesses, pyoderma, anal sacculitis and gingivitis).
CONTRA-INDICATIONS:
In common with all other penicillins, Synulox should not be administered to rabbits, guinea pigs, hamsters or gerbils.
Caution is advised in its use in any other very small herbivores. Use of the product may occasionally result in pain on injection and/or local tissue reaction.
Operator warnings Penicillins and cephalosporins may cause hypersensitivity (allergy) following injection, inhalation, ingestion or skin contact. Hypersensitivity to penicillins may lead to cross-reactions to cephalosporins and vice versa. Allergic reactions to these substances may occasionally be serious.
Do not handle this product if you know you are sensitised, or if you have been advised not to work with such preparations. Handle this product with great care to avoid exposure, taking all recommended precautions.
If you develop symptoms following exposure such as a skin rash, you should seek medical advice and show the doctor this warning. Swelling of the face, lips or eyes or difficulty with breathing, are more serious symptoms and require urgent medical attention. Wash hands after use.
WITHDRAWAL PERIOD:
Milk for human consumption must not be taken during treatment.
Milk for human consumption may only be taken only from cows after 60 hours from the last treatment.
Animals must not be slaughtered for human consumption during treatment.
Cattle may be slaughtered for human consumption only after 42 days from the last treatment.
Pigs may be slaughtered for human consumption only after 31 days from the last treatment.
Pharmaceutical precautions
Do not store above 25°C. Keep out of the reach of children. For animal treatment only.
This product does not contain an antimicrobial preservative.
Following withdrawal of the first dose, use the product within 28 days. Discard unused material. Swab the septum before removing each dose.
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.
