PREVICOX 227MG 30 Chewable Tablets

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PREVICOX 227MG 30 Chewable Tablets View larger



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Used for : tracheal mite treatment in, varroa treatment in the Abeil, varoa

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For warnings, precautions for use and against-indications, please see the instructions for use

PREVICOX 227MG 30 Chewable Tablets


Relief of pain and inflammation associated with osteoarthritis in dogs.
Relief of postoperative pain and inflammation associated with soft tissue surgery, orthopedic surgery and dental surgery in dogs.



Administer 5 mg / kg body weight once daily according to the table below.
The tablets may be mixed or unmixed to food.
The duration of treatment varies depending on response. Since the duration of field studies were limited to 90 days, the establishment of a longer treatment should be carefully evaluated and undergo regular veterinary care.
Relief of postoperative pain
Administering a daily dose of 5 mg / kg body weight according to the table below, up to 3 days if required. The first dose is administered about 2 hours before the operation.
After orthopedic surgery and following the observed response, treatment can be continued after the first 3 days of the same daily dosage and left to the judgment of the attending veterinarian.


Qualitative and quantitative composition
Each tablet contains:
active ingredient Firocoxib 57 mg / 227 mg Firocoxib.
Excipients iron oxide E172. Caramel E150d.
For excipients see section 'List of excipients ".
Pharmaceutical form Chewable Tablets. Light brown tablets engraved and scored convex round.

Precaution of use

Do not use in pregnant or lactating bitches.
Do not use in animals under 10 weeks or weighing less than 3 kg.
Do not use in animals with gastrointestinal bleeding, blood dyscrasia or haemorrhagic disorders.
Do not use concomitantly with corticosteroids or other anti-inflammatory steroids Idiens NSAIDs.
Special warnings for each target species
Special precautions for use in animals
Do not exceed the recommended dose regimen.
Use in very young animals, or animals with renal failure, suspected or confirmed heart or liver, may cause additional risks. If such use can not be avoided, it must be done under strict veterinary supervision.
Avoid use in dehydrated animals, hypovolemia or hypotension, due to the increased risk of renal toxicity. Avoid association with products with nephrotoxic potential.
If risk of gastrointestinal bleeding or in case of known intolerance to NSAIDs, the product must be used under strict veterinary control. Renal and / or hepatic disorders have been reported very rarely in dogs that received the recommended dose treatment. It is possible that a proportion of such cases is due to a hepatic disease or renal subclinical prior to start of treatment. It is therefore recommended to perform laboratory tests to determine the biochemical parameters of basic renal or hepatic functions before starting treatment and periodically during treatment.
Treatment should be discontinued in the presence of the following signs: repeated diarrhea, vomiting, occult blood in faeces, sudden weight loss, anorexia, lethargy, degradation of renal or hepatic biochemistry parameters.
Special precautions to be taken by the person administering the drug to animals
Wash hands after using the product.
In case of accidental ingestion, seek medical advice immediately and show the package insert or label.
Return the unused half tablets to the blister and keep out of reach of children.
Adverse reactions (frequency and seriousness)
Vomiting and diarrhea have occasionally been reported. These reactions are usually transient and reversible upon discontinuation of treatment. Renal and / or hepatic disorders have been reported very rarely in dogs that received the recommended dose treatment. In rare cases, nervous symptoms have been reported in dogs.
If side effects like vomiting, repeated diarrhea, blood in faeces, sudden weight loss, anorexia, lethargy, degradation of renal or hepatic biochemistry parameters, treatment should be discontinued and a veterinarian should be consulted. As when using other NSAIDs, serious side effects can occur and, in very rare cases can be fatal.
* The frequency of possible adverse effects is defined using the following convention:
Rare affects 1 to 10 animals 10 000
Very rare affects less than 1 animal in 10 000
Use during pregnancy, or lactation and lay
Do not use in pregnant or lactating bitches.
Laboratory studies on rabbits have shown maternotoxic and foetotoxic effects at doses similar to those recommended for the dog.
Drug interactions and other forms of interaction
Pre-treatment with other anti-inflammatory drugs may result in additional or increased adverse effects. It is therefore recommended to observe a period of 24 hours without treatment before beginning treatment with Previcox. The duration of this transition period must be adapted according to the pharmacokinetic properties of the products used previously.
Do not administer Previcox simultaneously with other NSAIDs or glucocorticosteroids. Ulceration of the gastrointestinal tract may be exacerbated by corticosteroids in animals given non-steroidal anti-inflammatory products were administered.
Simultaneous treatment with molecules having an effect on renal blood flow, such as diuretics or inhibitors of angiotensin converting enzyme ACE inhibitors, should be subject to clinical monitoring. Any combination with other potentially nephrotoxic drugs should be avoided due to an increased risk of renal toxicity. Anesthetics may affect renal perfusion, parenteral fluid intake should be considered during the operation to reduce potential renal complications when using NSAIDs peri-operatively.
Concurrent use of other active ingredients highly protein bound may compete with firocoxib for binding sites, and therefore have toxic effects.

Warnings about medications

Attention, the drug is not a product like any other. Read the package leaflet before ordering. Do not let drugs out of reach of children. If symptoms persist, seek the advice of your doctor or pharmacist. Beware of incompatibilities on your current products.

Tell your pharmacist Online ongoing treatment to identify any incompatibilities. The order confirmation form contains a custom message field provided for this purpose.

Click here to find the manual of this drug on the website of the National Agency of Drug Safety and health products.

Pharmacovigilance : Declare one or effect (s) undesirable (s) connected (s) to the use of a drug

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