Equioxx paste

Equioxx paste

Product Code: Equioxx
Availability:
In Stock
Price: £10.91 Ex Tax: £10.91

This product requires a prescription

Before we can despatch this product we need sight of a prescription - please therefore read the options below and then select the correct option from the drop-down:

1) New Prescription - I have a prescription for this product. Please post your prescription to the address below and ensure that your order number is noted on the prescription: East Kent Equine, 21 Mill Road, Deal, Kent CT14 9AH

2) Repeat Prescription – East Kent Equine have the prescription for this product already. Your product request will be checked against the prescription held at East Kent Equine and despatched accordingly.

3) East Kent Equine Client - I do not have a prescription for this product but I am a client of East Kent Equine. Our vets will consider your request and be in contact shortly to carry out any examinations before despatching the product if needed.

Orders containing both prescription and non-prescription products will only be despatched once the prescription has been received.
Medications and drugs are non-returnable.

Description

Equioxx is off-white oral paste containing firocoxib, a non-steroidal drug used to alleviate pain and inflammation in horses. 

Clinical particulars

Target species

Horses.

Indications for use

Alleviation of pain and inflammation associated with osteoarthritis and reduction of associated lameness in horses.

Contra-indications

Do not use in animals suffering from gastrointestinal disorders and haemorrhage, impaired hepatic, cardiac or renal function and bleeding disorders. Do not use in breeding, pregnant or lactating mares.

Do not use concomitantly with corticosteroids or other non-steroidal anti-inflammatory drugs (NSAIDs). Do not use in case of hypersensitivity to the active substance or to any of the excipients.

Special warnings for each target species

None.

Special precautions for use in animals

Do not use in animals less than 10 weeks. If side effects occur, treatment should be discontinued and the advice of a veterinarian should be sought. Avoid use in any dehydrated, hypovolaemic or hypotensive animal, as there may be potential risk of increased renal toxicity. Concurrent administration of potentially nephrotoxic veterinary medicinal products should be avoided. The recommended treatment dose and duration should not be exceeded.

Special precautions to be taken by the person administering the product to animals

In case of accidental ingestion, seek medical advice immediately and show the package leaflet or the label to the physician. Avoid contact with eyes and skin. If it occurs, rinse affected area immediately with water. Wash hands after use of the product. Like other medicinal products that inhibit COX-2, pregnant women or women attempting to conceive should avoid contact with, or wear disposable gloves, when administering the product.

Adverse reactions

Lesions (erosion/ulceration) of the oral mucosa and of the skin around the mouth may occasionally be observed in treated animals. Typically, these lesions are mild and resolve without treatment, but oral lesions may be associated with salivation and labial and tongue oedema.

Use during pregnancy, lactation or lay

No data is available in horses, however, studies in other animals have shown embryo-foetotoxicity, malformations, delayed parturition and decreased pup survival. Therefore, do not use in breeding, pregnant or lactating animals.

Interactions

Other NSAIDs, diuretics and substances with high protein binding may compete for binding and lead to toxic effects. Do not use concomitantly with corticosteroids or other NSAIDs.

Pre-treatment with other anti-inflammatory substances may result in additional or increased adverse effects and a treatment-free period with such products should be observed. The treatment-free period should take into account the pharmacological properties of the medicinal products used previously.

Concomitant treatment with molecules displaying action on renal flow (e.g. diuretics) should be subject to clinical monitoring. Concurrent administration of potentially nephrotoxic drugs should be avoided as there might be an increased risk of renal toxicity.

Amounts to be administered and administration route

Oral use.

Administer 0.1 mg firocoxib per kg bodyweight, once daily. Duration of treatment will be dependent on the response observed, but should not exceed 14 days.

To administer Equioxx at the dose of 0.1 mg firocoxib/kg, set the syringe plunger to the appropriate dose division for the horse’s weight. Each full dose division on the syringe plunger delivers sufficient firocoxib to treat 100 kg body weight. The contents of one syringe will treat horses weighing up to 600 kg. To ensure correct dosage, bodyweight should be determined as accurately as possible to avoid overdosing.

To deliver firocoxib at the appropriate dosage, unlock the knurled ring on the syringe plunger by rotating it ¼ turn and slide it along the plunger shaft to the appropriate dose division for the horse’s weight. Rotate the plunger ring ¼ turn to lock it in place and ensure it is locked.

Make sure the horse’s mouth contains no feed. Remove the cover from the tip of the syringe. Insert the syringe tip into the horse’s mouth at the interdental space and deposit the paste on the base of the tongue.

Overdose

Lesions (erosion/ulceration) of the oral mucosa and of the skin around the mouth may occasionally be observed in treated animals when administered the recommended treatment dose. Typically, these lesions are mild and resolve without treatment, but oral lesions may be associated with salivation and labial and tongue oedema. The incidence of oral/skin lesions increases with increasing dose.

At high dosages and prolonged treatment (3 times the recommended dose for 42 consecutive days and 2.5 times the recommended dose for 92 consecutive days administered once daily) mild to moderate renal lesions were observed. If clinical signs occur, treatment should be discontinued and symptomatic treatment initiated.

Withdrawal periods

Meat and offal: 26 days.

Do not use in mares producing milk for human consumption.

 

Pharmaceutical particulars

Excipients

Titanium dioxide (E 171), Glycerol triacetate, Silica colloidal anhydrous, Magnesium carbonate heavy, Macrogol 300.

Major incompatibilities

Not applicable.

Shelf life

Shelf life of the product as packaged for sale: 3 years.

Shelf life after first opening the syringe: 3 months.

Special precautions for storage

Replace cap after use. This product does not require any special storage conditions.

Immediate packaging

Carton box containing 1 syringe with 7.32 g of oral paste labelled in 100 kg dosing increments.

Disposal

Any unused product or waste materials derived from such products should be disposed of in accordance with local requirements.

 

Legal category

POM-V

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