Online Pet Medications & Pet Supplies

Synulox Rtu

Category: S

Temporarily Out of Stock



4.1 Target species Cattle, pigs, dogs and cats. 4.2 Indications for use, specifying the target species This product has bactericidal activity against a broad spectrum of clinically important bacteria found in large and small animals. In vitro the product is active against a wide range of bacteria, including strains resistant to amoxicillin alone because of beta-lactamase production: Gram-positive Actinomyces bovis Bacillus anthracis Clostridia Corynebacteria Peptostreptococcus spp. Staphylococci Streptococci Gram-negative Actinobacillus lignierisi Actinobacillus pleuropneumoniae Bacteroides Bordetella bronchiseptica Campylobacter spp. Escherichia coli Fusobacterium necrophorum Haemophilus spp. Klebsiellae Moraxella spp. Pasteurellae Proteus spp. Salmonellae Clinically the product is indicated for the treatment of diseases including: Cattle Respiratory infections, soft tissue infections (e.g. joint-ill/navel-ill, abscesses etc.), metritis and mastitis. Combined Therapy for the treatment of bovine mastitis: In the situation where systemic treatment as well as intramammary treatment is necessary, Synulox Ready-to-Use injection can be used in combination with Synulox Lactating Cow Intramammary. Pigs Respiratory bacterial infections in growing pigs. Colibacillosis. Periparturient infections in sows (e.g. mastitis, metritis and agalactia.) Dogs and Cats Respiratory tract infections, urinary tract infections and skin and soft tissue infections (e.g. abscesses, pyoderma, anal sacculitis, gingivitis). 4.3 Contraindications The product should not be administered to rabbits, guinea pigs, hamsters or gerbils. Caution is advised in its use in other very small herbivores. 4.4 Special warnings for each target species None. 4.5 Special precautions for use i) Special precautions for use in animals Care should be taken to avoid contaminating the remaining contents of a vial with water. Clavulanic acid is moisture sensitive. It is very important that a completely dry syringe is used when extracting the 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. ii) Special precautions to be taken by the person administering the veterinary medicinal product to animals 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. 4.6 Adverse reactions (frequency and seriousness) Use of the product may occasionally result in pain on injection and/or local tissue reactions. 4.7 Use during pregnancy, lactation or lay The product may be used in pregnant animals, subject to observance of the withholding time for milk and the withdrawal time for meat intended for human consumption. 4.8 Interaction with other medicinal products and other forms of interaction None known.

Our Standard Delivery - £6.75

Royal Mail Tracked 24 (Signed For)

  • Next business day service
  • Compensation cover up to £100
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Any orders placed after close of business on Thursday will not be delivered until Tuesday

 

 

 

Our Express Delivery - £10.45

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Please note that all chilled deliveries must be sent on an Express service.

Chilled orders placed after close of business on Wednesday will not be despatched until Monday

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Category POM-V
Temperature Ambient
MA/VM/EU No: 42058/4148
Species
  • cats
  • cattle
  • dogs
  • pigs
VMD Link https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_141401.PDF
NOAH Link
Dosage By either intramuscular or subcutaneous injection in dogs and cats, and by intramuscular injection only in cattle and pigs, at a dosage rate of 8.75 mg/kg bodyweight (1 ml / 20 kg bodyweight) daily for 3-5 days. Shake the vial well before use. After injection, massage the injection site. Use a completely dry sterile needle and syringe. Swab the septum before removing each dose. For combined therapy, the following minimum treatment regime should be followed:   Synulox RTU Synulox LC 8.75 mg/kg bodyweight (7.0 mg amoxicillin, 1.75 mg clavulanic acid) i.e. 1 ml/20 kg bodyweight 24 hours 8.75 mg/kg bodyweight (7.0 mg amoxicillin, 1.75 mg clavulanic acid) i.e. 1 ml/20 kg bodyweight 24 hours 8.75 mg/kg bodyweight (7.0 mg amoxicillin, 1.75 mg clavulanic acid) i.e. 1 ml/20 kg bodyweight Where necessary, Synulox RTU Injection may be administered for an additional two days for a total of 5 daily injections One syringe gently infused into the teat of the infected quarter 12 hours One syringe gently infused into the teat of the infected quarter 12 hours One syringe gently infused into the teat of the infected quarter 4.10 Overdose (symptoms, emergency procedures, antidotes), if necessary Synulox is of a low order of toxicity and is well tolerated by the parenteral route. Apart from occasional injection site reactions, which may occur at the recommended dose, no other adverse effects are to be expected from an accidental overdose.
Withdrawals Milk for human consumption must not be taken during treatment. Milk for human consumption may only be taken from cattle at 60 hours (5th milking, if cows are milked twice daily). 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. Combined Therapy: When using Synulox LC Intramammary and Synulox RTU in combination, animals must not be slaughtered for human consumption during treatment. Cows may not be slaughtered for human consumption until 42 days after the last treatment. Milk must not be taken for human consumption during treatment. Milk for human consumption may be taken only from cows after 60 hours from the last treatment of Synulox RTU following the minimum posology regime as described in Section 4.9.