Animeloxan 20mg/ml solution for injection for cattle, pigs and horses 100ml

   Product Ref: FOANI02 Category: A

£ 80.69

Vat Rate: 20%

Prescription Required

4.1 Target species Cattle, pigs and horses 4.2 Indications for use, specifying the target species Cattle: For use in acute respiratory infection with appropriate antibiotic therapy to reduce clinical signs in cattle. For use in diarrhoea in combination with oral re-hydration therapy to reduce clinical signs in calves of over one week of age and young, non-lactating cattle. For adjunctive therapy in the treatment of acute mastitis, in combination with antibiotic therapy. For the relief of post-operative pain following dehorning in calves. Pigs: For use in non-infectious locomotor disorders to reduce the symptoms of lameness and inflammation. For adjunctive therapy in the treatment of puerperal septicaemia and toxaemia (mastitis-metritis-agalactia syndrome) with appropriate antibiotic therapy. Horses: For use in the alleviation of inflammation and relief of pain in both acute and chronic musculo-skeletal disorders. For the relief of pain associated with equine colic. 4.3 Contraindications See also section 4.7. Do not use in horses less than 6 weeks of age. Do not use in animals suffering from impaired hepatic, cardiac or renal function and haemorrhagic disorders, or where there is evidence of ulcerogenic gastrointestinal lesions. Do not use in cases of hypersensitivity to the active substance or to any of the excipients. For the treatment of diarrhoea in cattle, do not use in animals of less than one week of age. 4.4 Special warnings for each target species Treatment of calves with Animeloxan 20 minutes before dehorning reduces post-operative pain. Animeloxan alone will not provide adequate pain relief during the dehorning procedure. To obtain adequate pain relief during surgery co-medication with an appropriate analgesic is needed. 4. 5 Special precautions for use Special precautions for use in animals If adverse reactions occur, treatment should be discontinued and the advice of a veterinarian should be sought. Avoid use in very severely dehydrated, hypovolaemic or hypotensive animals which require parenteral rehydration, as there may be a potential risk of renal toxicity. In case of inadequate relief of pain when used in the treatment of equine colic, careful re-evaluation of the diagnosis should be made as this could indicate the need for surgical intervention. Special precautions to be taken by the person administering the veterinary medicinal product to animals Accidental self-injection may give rise to pain. People with known hypersensitivity to non-steroidal anti-inflammatory drugs (NSAIDs) should avoid contact with the veterinary medicinal product. In case of accidental self-injection, seek medical advice immediately and show the package leaflet or the label to the physician. If accidental skin contact occurs, wash the affected area thoroughly. Wash hands after use. In view of the risk of accidental self-injection and the known adverse class-effects of NSAIDs and other prostaglandin inhibitors on pregnancy and/or embryofoetal development, the veterinary medicinal product should not be administered by pregnant women or women attempting to conceive. 4.6 Adverse reactions (frequency and seriousness) In cattle, a single subcutaneous injection can cause a non-painful swelling that lasts up to 23 days. Intravenous injection is generally well-tolerated. In pigs, two consecutive intramuscular injections have a local irritant effect that can last up to 9 days. In horses, a transient swelling at the injection site can occur but resolves without intervention. In rare cases anaphylactoid reactions, which may be serious (including fatal), may occur and should be treated symptomatically. The frequency of adverse reactions is defined using the following convention: - very common (more than 1 in 10 animals treated displaying adverse reaction(s)) - common (more than 1 but less than 10 animals in 100 animals treated ) - uncommon (more than 1 but less than 10 animals in 1,000 animals treated) - rare (more than 1 but less than 10 animals in 10,000 animals treated) - very rare (less than 1 animal in 10,000 animals treated, including isolated reports). 4.7 Use during pregnancy, lactation or lay Cattle and pigs: Can be used during pregnancy and lactation. Horses: Do not use in pregnant or lactating mares. See also section 4.3. 4.8 Interaction with other medicinal products and other forms of interaction Do not administer concurrently with glucocorticosteroids, other non-steroidal anti-inflammatory drugs or with anti-coagulant agents.
Vat Rate: 20%

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Category POM-V
Temperature Ambient
MA/VM/EU No: 24745/4015
  • cattle
  • horse
  • pig
VMD Link Product Information Database (
Dosage 4.9 Amounts to be administered and administration route Cattle: Single subcutaneous or intravenous use at a dosage of 0.5 mg meloxicam/kg body weight (i.e. 2.5 ml/100 kg body weight) in combination with antibiotic therapy or with oral re-hydration therapy, as appropriate. Pigs: Single intramuscular use at a dosage of 0.4 mg meloxicam/kg body weight (i.e. 2.0 ml/100 kg body weight) in combination with antibiotic therapy, as appropriate. If required, a second administration of meloxicam can be given after 24 hours. Alternating injection sites are recommended. Horses: Single intravenous use at a dosage of 0.6 mg meloxicam/kg body weight (i.e. 3.0 ml/100 kg body weight). 4.10 Overdose (symptoms, emergency procedures, antidotes), if necessary In the case of overdosage symptomatic treatment should be initiated.
Withdrawals 4.11 Withdrawal period(s) Cattle: Meat and offal: 15 days Milk: 5 days Pigs: Meat and offal: 8 days Horses: Meat and offal: 5 days Do not use in horses producing milk for human consumption.