Nuflor Injection 100ml

Category: N

Temporarily Out of Stock



Target species Cattle and sheep. Indications for use Cattle: Diseases caused by florfenicol susceptible bacteria. Metaphylactic and therapeutic treatment of respiratory tract infections in cattle due to Mannheimia haemolytica, Pasteurella multocida and Histophilus somni. The presence of the disease in the herd should be established before metaphylactic treatment. Sheep: Treatment of ovine respiratory tract infections due to M. haemolytica and P. multocida susceptible to florfenicol. Contraindications Do not use in adult bulls and rams intended for breeding purposes. Do not use in the case of known hypersensitivity to the active substance or to any of the excipients. Special warnings for each target species None. Special precautions for use The product should be used in conjunction with susceptibility testing and take into account official and local antimicrobial policies. The safety of the product has not been established in sheep younger than 7 weeks of age. Operator warnings People with known hypersensitivity to propylene glycol and polyethylene glycols should avoid contact with the veterinary medicinal product. In case of accidental contact with skin or eyes, rinse immediately with plenty of water. In case of accidental self-injection, seek medical advice immediately and show the package leaflet or label to the physician. Adverse reactions Cattle: A decrease in food consumption and transient softening of the faeces may occur during the treatment period. The treated animals recover quickly and completely upon termination of treatment. Intramuscular and subcutaneous administration may cause inflammatory lesions at the injection site which may persist for 14 days. In very rare cases, anaphylactic shock has been reported in cattle. Sheep: A decrease in food consumption may occur during the treatment period. The treated animals recover quickly and completely upon termination of treatment. Intramuscular administration may cause inflammatory lesions at the injection site which may persist up to 28 days. Typically, these are mild and transient. Use during pregnancy or lactation Studies in laboratory animals have not revealed any evidence of teratogenic or foetotoxic effects. However, the effect of florfenicol on bovine and ovine reproductive performance and pregnancy has not been assessed. Use only according to the benefit/risk assessment by the responsible veterinarian. Interactions No data available.

Royal Mail 2nd Class / Parcel Force 48

UK to UK :Normally arrives in 2-4 business days.

UK to Ireland :Normally arrives in 4-6 business days

UK to EU Countries : Normally arrives in 6-10 working days depending on where the parcel is going

 

Please note standered delivery is none trackable , none insured , no responsabily for lose or Damage

 

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Royal Mail First Class / Parcel Force 24

UK to UK :Normally arrives in 1-2 business days.

UK to Ireland 3-4 business days

UK to EU Countries : Normally arrives in 6-10 working days depending on where the parcel is going

 

Please note :Trackable , Royal Mail insured up to £50.

 

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Parcel Force Express AM Guaranteed before Midday.

UK to UK only . UP to 5KG Max Weight

Arrives next day before 12 noon, requires a signature.

 

Parcel Forcel Terms & Conditions apply

 

Important: Parcel Force advise that there are some postcodes where an extended delivery time exists, and may affect the date of delivery or the service is not available.

 

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Category POM-V
Temperature Ambient
MA/VM/EU No: 01708/4574
Species
  • cattle
  • sheep
VMD Link Product Information Database (defra.gov.uk)
NOAH Link https://www.noahcompendium.co.uk/?id=-455585
Dosage Amounts to be administered and administration route Swab septum before removing each dose. Use a dry sterile needle and syringe. To ensure a correct dosage body weight should be determined as accurately as possible to avoid underdosing. The vials should not be broached more than 20 times. User should therefore select the most appropriate vial size according to the target species to be treated. When treating groups of animals at the same time, use of a draw-off needle in the vial stopper is recommended to avoid excess stopper broaching. The draw-off needle should be removed after treatment. For treatment Cattle: Intramuscular use: 20 mg/kg bodyweight (1ml/15kg) to be administered twice 48 hours apart using a 16 gauge needle. Subcutaneous use: 40 mg/kg bodyweight (2ml/15kg) to be administered once only using a 16 gauge needle. The dose volume given at any one injection site should not exceed 10 ml. The injection should only be given in the neck. Sheep: Intramuscular use: 20 mg florfenicol/kg bodyweight (1 ml/15 kg) to be administered daily for three consecutive days. The volume administered per injection site should not exceed 4 ml. Pharmacokinetic studies showed that mean plasma concentrations remain above MIC90 (1 μg/ml) for up to 18 hours after administration of the product at the recommended treatment dose. The pre-clinical data supported the recommended treatment interval (24 hours) for target pathogens with MIC up to 1 μg/ml. For metaphylaxis Cattle: Subcutaneous use: 40 mg/kg bodyweight (2ml/15kg) to be administered once only using a 16 gauge needle. The dose volume given at any one injection site should not exceed 10 ml. The injection should only be given in the neck. Overdose Cattle: No symptoms other than those described under Adverse reactions above. In cattle, a decrease in food consumption and transient softening of the faeces may occur during the treatment period. The treated animals recover quickly and completely upon termination of treatment. Sheep: After administration of 3 times the recommended dose or more a transient reduction in feed and water consumption has been observed. Additional effects included an increased incidence of lethargy, emaciation and loose faeces. Head tilt was seen after administration of 5 times the recommended dose and was considered most likely a result of irritation at the injection site.
Withdrawals Withdrawal period Meat and offal: Cattle: IM use (20 mg/kg bodyweight, twice): 30 days. SC use (40 mg/kg bodyweight, once): 44 days. Sheep: 39 days. Milk: Not authorised for use in animals producing milk for human consumption including pregnant animals intended to produce milk for human consumption.