Equioxx 8.2 mg/g Oral Paste for Horses
Active ingredient: Firocoxib
Form
Paste
Species
Manufacturer
AUDEVARD
VMD MA No.
44684/5002
What it's used for
Alleviation of pain and inflammation associated with osteoarthritis and reduction of associated lameness in horses.
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Prescription required
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Equioxx 8.2 mg/g Oral Paste for Horses — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.
associated lameness in horses.
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.
impaired hepatic, cardiac or renal function and bleeding disorders.
Do not use in breeding, pregnant or lactating animals (see section 4.7).
Do not use concomitantly with corticosteroids or other non-steroidal anti-inflammatory
drugs (NSAIDs) (see section 4.8).
Do not use in case of hypersensitivity to the active substance or to any of the excipients.
very commonly observed in treated animals during tolerance studies. These lesions
were mild and resolved without treatment. Salivation and labial and tongue oedema
have been uncommonly associated with the oral lesions in a field study.
The frequency of adverse reactions is defined using the following convention:
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treated)
Issued: March 2022
AN: 02783/2021
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 veterinary medicinal
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 veterinary medicinal 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 veterinary medicinal product.
Issued: March 2022
AN: 02783/2021
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 medicinal products
should therefore 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 medicinal products should be avoided as there might be an increased risk
of renal toxicity.
This veterinary medicinal product does not require any special storage conditions.
Not authorized for use in animals producing milk for human consumption.
5.
This information is sourced from the official Summary of Product Characteristics (SPC) published by the Veterinary Medicines Directorate (VMD). It is provided for informational purposes only and does not replace professional veterinary advice. Always consult your vet before administering any medication.
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Other Products Containing Firocoxib
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
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