Overview

This is a summary of the European public assessment report (EPAR). Its purpose is to explain how the assessment done by the Committee for Medicinal Products for Veterinary Use (CVMP) on the basis of the documentation provided, led to the recommendations on the conditions of use.

This summary cannot replace a face-to-face discussion with your veterinarian. If you need more information about your animal’s medical condition or treatment, contact your veterinarian. If you want more information on the basis of the CVMP recommendations, read the scientific discussion (also part of the EPAR).

Meloxidyl is a medicinal product that contains the active substance meloxicam. Meloxidyl is a pale green oral suspension (1.5 mg/ml) for dogs and (0.5 mg/ml) for cats, which is mixed into the food, and a yellow solution for injection (5 mg/ml) for dogs and cats as well as solution for injection (20 mg/ml) for cattle, pigs and horses.

Meloxidyl is a ‘generic’: this means that Meloxidyl is similar to a ‘reference veterinary medicinal product’ already authorised in the European Union (EU; Metacam). Studies have been carried out to prove that Meloxidyl is ‘bioequivalent’ to the reference veterinary medicinal product: this means that Meloxidyl is equivalent to Metacam in the way it is absorbed and used by the body.

In dogs, Meloxidyl is used as an oral suspension to relieve inflammation and pain in musculoskeletal disorders. It can be used for both acute (sudden) disorders, such as those seen after an injury, and chronic (long-term) disorders. As an injection, Meloxidyl is also used to reduce the pain and inflammation after an operation, such as orthopaedic or soft-tissue surgery.

In cats, Meloxidyl is used as an oral suspension to relieve inflammation and pain in chronic musculoskeletal disorders as well as to relieve mild to moderate pain after an operation, such as spaying or soft-tissue surgery. Meloxidyl injection is used in cats to reduce the pain after an operation, such as spaying or minor soft-tissue surgery.

In cattle, Meloxidyl injection is used to reduce clinical signs in case of acute respiratory infection with appropriate antibiotic therapy, to reduce clinical signs in case of diarrhoea in combination with oral rehydration therapy in calves over one week of age and young, non-lactating cattle and as supportive therapy in the treatment of acute mastitis, in combination with antibiotics.

In pigs, Meloxidyl injection is used to reduce the symptoms of lameness and inflammation in non-infectious locomotor disorders and for supportive therapy in the treatment of puerperal septicaemia and toxaemia around farrowing (mastitis-metritis-agalactia syndrome) with appropriate antibiotics.

In horses, Meloxidyl injection is used to relieve inflammation and pain in both acute and chronic musculoskeletal disorders and for the relief of pain associated with colic.

Meloxidyl contains meloxicam, which belongs to a class of medicines called non-steroidal anti-inflammatory drugs (NSAIDs). Meloxicam acts by inhibition of prostaglandin synthesis. As the prostaglandins are substances that trigger inflammation, pain, exudation and fever, meloxicam reduces those responses.

A study looked at how Meloxidyl was absorbed and its effects in the body, in comparison with Metacam.

Based on the findings of the study, Meloxidyl was considered to be bioequivalent to the reference medicinal product. Because of this, Meloxidyl’s benefit is taken as being the same as that of the reference medicinal product.

In dogs and cats, the side effects seen with Meloxidyl are similar to those seen with other NSAIDs and occur only occasionally. They include loss of appetite, vomiting, diarrhoea, blood in the stools and apathy (lack of vitality). They usually occur during the first week of treatment and tend to be temporary. They disappear once treatment has stopped. In very rare cases, they may be serious or fatal.

In cattle and pigs, subcutaneous, intramuscular and intravenous administration are well tolerated. Only a slight temporary swelling at the injection site following subcutaneous administration was observed in less than 10% of the cattle treated in clinical studies.

In horses, anaphlylactoid (hypersensitivity) reactions can occur and should be treated symptomatically. A temporary swelling at the injection site can occur but resolves without intervention.

People who are hypersensitive to NSAIDs should avoid contact with Meloxidyl. If someone swallows the medicinal product, the advice of a doctor should be sought immediately. Accidental self-injection may cause pain. If this happens, seek medical advice immediately and show the package leaflet or the label to the doctor.

After the last administration of Meloxidyl cattle should not be slaughtered for 15 days and the milk not used for 5 days. Pigs and horses should not be slaughtered for 5 days.

The Committee for Medicinal Products for Veterinary Use (CVMP) concluded that, in accordance with EU requirements, Meloxidyl has been shown to be bioequivalent to Metacam. Therefore the CVMP’s view was that, as for Metacam, Meloxidyl’s benefits are greater than its risks. The Committee recommended that Meloxidyl should be given a marketing authorisation. The benefit-risk balance may be found in module 6 of this EPAR.

The European Commission granted a marketing authorisation valid throughout the European Union for Meloxidyl to Ceva Santé Animale on 15 January 2007. Information on the prescription status of this product may be found on the label of the carton.

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Product information

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Latest procedure affecting product information: IA/0028/G

31/01/2019

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Product details

Name of medicine
Meloxidyl
Active substance
meloxicam
International non-proprietary name (INN) or common name
meloxicam
Species
  • Dogs
  • Cats
  • Cattle
  • Pigs
  • Horses
Anatomical therapeutic chemical veterinary (ATCvet) code
QM01AC06

Pharmacotherapeutic group

Oxicams

Therapeutic indication

Dogs

Alleviation of inflammation and pain in both acute and chronic musculoskeletal disorders.

Reduction of post-operative pain and inflammation following orthopaedic and soft-tissue surgery.

Cats

Reduction of post-operative pain after ovariohysterectomy and minor soft-tissue surgery.

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 rehydration 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.

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 musculoskeletal disorders.

For the relief of pain associated with equine colic.

Authorisation details

EMA product number
EMEA/V/C/000115

Generic

This is a generic medicine, which is developed to be the same as a medicine that has already been authorised, called the reference medicine. A generic medicine contains the same active substance(s) as the reference medicine, and is used at the same dose(s) to treat the same disease(s). For more information, see Generic and hybrid medicines.

Marketing authorisation holder
Ceva Santé Animale

10 avenue de la Ballastière
33500 Libourne
France

Marketing authorisation issued
15/01/2007
Revision
14

Assessment history

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