Ficoxil 57 mg Chewable Tablets for Dogs
Active ingredient: Firocoxib
Form
Chewable
Species
Manufacturer
Industrial Veterinaria SA
VMD MA No.
36547/3016
What it's used for
For the relief of pain and inflammation associated with osteoarthritis in dogs. For the relief of post-operative pain and inflammation associated with soft...
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Ficoxil 57 mg Chewable Tablets for Dogs — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 26 Mar 2026.
For the relief of post-operative pain and inflammation associated with soft-tissue,
orthopaedic and dental surgery in dogs.
Revised: November 2025
AN: 02244/2025
Osteoarthritis:
Administer 5 mg firocoxib per kg bodyweight once daily as presented in the table
below.
Duration of treatment will be dependent on the response observed. As field studies
were limited to 90 days, longer-term treatment should be considered carefully and
regular monitoring undertaken by the veterinarian.
Relief of post-operative pain:
Administer 5 mg firocoxib per kg bodyweight once daily as presented in the table below
for up to 3 days as needed, starting approximately 2 hours prior to surgery.
Following orthopaedic surgery and depending on the response observed, treatment
using the same daily dosing schedule may be continued after the first 3 days, upon
judgement of the attending veterinarian.
The following table is intended as a guideline for administering the veterinary medicinal
product at the recommended dose.
Number of tablets by size
Body weight (kg)
57 mg227 mg
mg/kg range
3.0 – 5.5½5.2 – 9.55.6- 7.5¾5.7 – 7.67.6-101 or ¼5.7 – 7.510.1- 131 ¼5.5 – 7.113.1 - 161 ½5.3 – 6.516.1-18.51 ¾5.4 – 6.218.6-22.5½5.0 – 6.122.6-34¾5.0 – 7.534.1-4515.0 – 6.745.1-561 ¼5.1 – 6.356.1-681 ½5.0 – 6.168.1-791 ¾5.0 – 5.879.1-9025.0 – 5.7
= ¼ Tablet = ½ Tablet = ¾ Tablet = 1 Tablet
Revised: November 2025
AN: 02244/2025
Tablets can be divided into 2 or 4 equal parts to ensure accurate dosing.
Tablets can be administered with or without food.
Do not use in animals less than 10 weeks of age or less than 3 kg body weight.
Do not use in animals suffering from gastrointestinal bleeding, blood dyscrasia or
haemorrhagic disorders.
Do not use concomitantly with corticosteroids or other non-steroidal anti-inflammatory
drugs (NSAIDs).
Do not use in known cases of hypersensitivity to the active substance or to any of the
excipients.
of a transitory nature and are reversible when the treatment is stopped. Renal and/or
hepatic disorders have been reported in very rare cases in dogs administered the
recommended treatment dose. Rarely, nervous system disorders have been reported
in treated dogs.
If adverse reactions like vomiting, repeated diarrhoea, faecal occult blood, sudden
weight loss, anorexia, lethargy, degradation of renal or hepatic biochemistry
parameters occur, use of the product should be stopped and the advice of a
veterinarian should be sought. As with other NSAIDs, serious adverse effects can
occur and, in very rare cases, may be fatal.
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).
Special precautions for use in animals
As the tablets are flavoured, they should be stored in a safe place out of the reach of
animals.
The recommended dose, as indicated in the dosing table, should not be exceeded.
Use in very young animals, or animals with suspected or confirmed impairment of
renal, cardiac or hepatic function may involve additional risk. If such use cannot be
avoided, those dogs require careful veterinary monitoring.
Avoid use in any dehydrated, hypovolaemic or hypotensive animals, as there is a
potential risk of increased renal toxicity. Concurrent administration of potentially
nephrotoxic drugs should be avoided.
Use this product under strict veterinary monitoring where there is a risk of
gastrointestinal bleeding, or if the animal previously displayed intolerance to NSAIDs.
Renal and/or hepatic disorders have been reported in very rare cases in dogs
administered the recommended treatment dose. It is possible that a proportion of such
cases had sub-clinical renal or hepatic disease prior to the commencement of therapy.
Therefore, appropriate laboratory testing to establish baseline renal or hepatic
biochemistry parameters is recommended prior to and periodically during
administration.
The treatment should be discontinued if any of these signs are observed: repeated
diarrhoea, vomiting, faecal occult blood, sudden weight loss, anorexia, lethargy,
degradation of renal or hepatic biochemistry parameters.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals
This product may be harmful following accidental ingestion.
In order to prevent children from accessing the product, tablets should be administered
and stored out of sight and reach of children. Halved or quartered tablets should be
returned to the open blister pocket and inserted into the outer carton.
Laboratory studies in rats and rabbits have shown evidence that firocoxib has the
potential to effect reproduction and to induce malformations in foetuses. Pregnant
women or women who are intending to become pregnant should administer the
product with caution.
Wash hands after use of the product.
Revised: November 2025
AN: 02244/2025
In the event of accidental ingestion of one or more tablets, seek medical advice
immediately and show the package leaflet or the label to the doctor.
increased adverse effects and accordingly a treatment-free period with such drugs
should be observed for at least 24 hours before the commencement of treatment with
the product. The treatment-free period, however, should take into account the
pharmacokinetic properties of the products used previously.
The product must not be administered in conjunction with other NSAIDs or
glucocorticosteroids. Gastrointestinal tract ulceration may be exacerbated by
corticosteroids in animals given non-steroidal anti-inflammatory drugs.
Concomitant treatment with molecules displaying action on renal flow, e.g. diuretics or
Angiotensin Converting Enzyme (ACE) inhibitors, 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. As anaesthetic drugs may
affect renal perfusion, the use of parenteral fluid therapy during surgery should be
considered to decrease potential renal complications when using NSAIDs peri-
operatively.
Concurrent use of other active substances that have a high degree of protein binding
may compete with firocoxib for binding and thus lead to toxic effects.
Revised: November 2025
AN: 02244/2025
Revised: November 2025
AN: 02244/2025
Any remaining tablet portion should be returned to the blister and given at the next
administration within 7 days.
Revised: November 2025
AN: 02244/2025
Tablets can be divided into 2 or 4 equal parts to ensure accurate dosing.
Tablets can be administered with or without food.
4.10 Overdose (symptoms, emergency procedures, antidotes), if necessary
In dogs ten weeks of age at the start of treatment at dose rates equal or greater to 25
mg/kg/day (5 times the recommended dose) for three months, the following signs of
toxicity were observed: bodyweight loss, poor appetite, changes in the liver
(accumulation of lipid), brain (vacuolisation), duodenum (ulcers) and death. At dose
rates equal or greater to 15 mg/kg/day (3 times the recommended dose) for six months,
similar clinical signs were observed, albeit that the severity and frequency were less
and duodenal ulcers were absent.
In those target animal safety studies, clinical signs of toxicity were reversible in some
dogs following cessation of therapy.
In dogs seven months of age at the start of treatment at dose rates greater than or
equal to 25 mg/kg/day (5 times the recommended dose) for six months, gastrointestinal
adverse effects, i.e. vomiting were observed.
Overdose studies were not conducted in animals over 14 months of age.
If clinical signs of overdosing are observed, discontinue treatment.
4.11 Withdrawal period(s)
Not applicable.
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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