Meloxidolor

meloxicam

  • Email
  • Help

About

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).

What is Meloxidolor?

Meloxidolor is a medicine that contains the active substance meloxicam. It is available as a solution for injection (5 mg/ml, 20 mg/ml and 40 mg/ml).

Meloxidolor is a ’generic’. This means that Meloxidolor is similar to a ‘reference veterinary medicine’ containing the same active substance, but it is also available at a higher strength. While the reference medicine, Metacam, is available as 5-mg/ml and 20-mg/ml solutions for injection, Meloxidolor is also available as a 40-mg/ml solution for injection.

What is Meloxidolor used for?

Meloxidolor solution for injection (5 mg/ml) can be used to relieve inflammation and pain in dogs following surgery involving the bones or soft tissue (tissue just below the skin), and in cats following ovariohysterectomy (spaying) and minor soft-tissue surgery.

Meloxidolor solution for injection (5 mg/ml and 20 mg/ml) is used in pigs to reduce the symptoms of lameness (inability to walk normally) and inflammation in noninfectious locomotor disorders (diseases that affect the ability to move). The 5-mg/ml solution for injection can also be used for the relief of postoperative pain associated with minor soft-tissue surgery such as castration (surgical removal of the testicles) and the 20-mg/ml solution for injection can be used together with appropriate antibiotic therapy for the treatment of diseases that occur after farrowing (giving birth) such as puerperal septicaemia (bacteria present in blood) and toxaemia (a toxic state) (mastitis-metritis-agalactia syndrome).

Meloxidolor solution for injection (5 mg/ml, 20 mg/ml and 40 mg/ml) is used in cattle, together with appropriate antibiotic therapy, to reduce signs of disease in acute respiratory infections (infection of the lungs and airways). It can be used in combination with oral rehydration therapy for diarrhoea (medicines given by mouth to restore water levels in the body) in calves of over one week of age and in young, non-lactating cattle. The 20-mg/ml and 40-mg/ml solutions for injection are also used in combination with antibiotic therapy to treat acute mastitis (inflammation of the udder).

Meloxidolor solution for injection (20 mg/ml and 40 mg/ml) is used in horses to relieve colic (abdominal pain) and the inflammation and pain in musculoskeletal disorders.

How does Meloxidolor work?

Meloxidolor contains meloxicam, which belongs to a class of medicines called non-steroidal anti-inflammatory drugs (NSAIDs). Meloxicam acts by blocking an enzyme called cyclo-oxygenase which is involved in the production of prostaglandins. As prostaglandins are substances that trigger inflammation, pain, exudation (fluid that leaks out of blood vessels during an inflammation) and fever, meloxicam reduces these signs of disease.

How has Meloxidolor been studied?

For intravenous use no studies in animals were needed as Meloxidolor contains the same active substance as the reference medicine Metacam. For subcutaneous and intramuscular use no studies were need for the 5-mg/ml and 20-mg/ml strengths as they contain the same concentration of active substance and have a similar composition to the reference product Metacam.

What benefit has Meloxidolor shown during the studies?

As Meloxidolor is considered to be bioequivalent to the reference medicine, its benefit is taken as being the same as that of the reference medicine. Two medicines are bioequivalent when they produce the same levels of the active substance in the body.

What is the risk associated with Meloxidolor?

Side effects sometimes seen with other NSAIDs, such as loss of appetite, vomiting, diarrhoea, blood appearing in the stools, renal (kidney) failure and apathy (lack of vitality) are occasionally seen with Meloxidolor in dogs and cats. In dogs, these generally occur within the first week of treatment and usually disappear once treatment has stopped. In very rare cases they may be serious or fatal.

A slight temporary swelling at the injection site following injection under the skin was observed in cattle and pigs. In horses, a temporary swelling at the injection site can occur but resolves without intervention.

In very rare cases, potentially serious or fatal anaphylactoid reactions (similar to severe allergic reactions) may occur following administration of the solution for injection and should be treated symptomatically.

Meloxidolor must not be used in animals with liver, heart or kidney problems, bleeding disorders, or suffering from irritation or ulcers of the digestive tract. It must not be used in animals which are hypersensitive (allergic) to the active substance or to any of the other ingredients.

Meloxidolor should not be used in pregnant or lactating dogs, cats and horses, but it can be used during pregnancy and lactation for cattle and pigs.

Meloxidolor must not be used in dogs, in cats or horses less than six weeks of age, in cattle less than one week of age when used in the treatment of diarrhoea or in pigs less than two days old. It must not be used in cats weighing less than 2 kilograms.

What are the precautions for the person who gives the medicine or comes into contact with the animal?

People who are hypersensitive (allergic) to NSAIDs should avoid contact with Meloxidolor. If someone accidentally injects themselves with the medicine, the advice of a doctor should be sought immediately.

Pregnant women and women of child-bearing potential should not administer Meloxidolor as meloxicam may be harmful for the foetus and unborn child.

What is the withdrawal period?

The withdrawal period is the time allowed after administration of the medicine before the animal can be slaughtered and the meat used for human consumption. It is also the time allowed after administration of the medicine before the milk can be used for human consumption.

Cattle

For meat the withdrawal period is 15 days and for milk it is five days.

Pigs

For meat the withdrawal period is five days.

Horses

For meat the withdrawal period is five days. The product is not authorised for use in horses producing milk for human consumption.

Why has Meloxidolor been approved?

The Committee for Medicinal Products for Veterinary Use (CVMP) considered that, in accordance with European Union requirements, Meloxidolor has been considered to be bioequivalent to Metacam. Therefore the CVMP’s view was that, as for Metacam, Meloxidolor’s benefits are greater than its risks when used for the approved indications and the Committee recommended that Meloxidolor be given a marketing authorisation. The benefit-risk balance may be found in the scientific discussion module of this EPAR.

Other information about Meloxidolor

The European Commission granted a marketing authorisation valid throughout the European Union for Meloxidolor on 22 April 2013. Information on the prescription status of this product may be found on the label / outer package.

Name Language First published Last updated
Meloxidolor : EPAR - Summary for the public BG = bălgarski 2013-05-13  
Meloxidolor : EPAR - Summary for the public ES = español 2013-05-13  
Meloxidolor : EPAR - Summary for the public CS = čeština 2013-05-13  
Meloxidolor : EPAR - Summary for the public DA = dansk 2013-05-13  
Meloxidolor : EPAR - Summary for the public DE = Deutsch 2013-05-13  
Meloxidolor : EPAR - Summary for the public ET = eesti keel 2013-05-13  
Meloxidolor : EPAR - Summary for the public EL = elliniká 2013-05-13  
Meloxidolor : EPAR - Summary for the public EN = English 2013-05-13  
Meloxidolor : EPAR - Summary for the public FR = français 2013-05-13  
Meloxidolor : EPAR - Summary for the public IT = italiano 2013-05-13  
Meloxidolor : EPAR - Summary for the public LV = latviešu valoda 2013-05-13  
Meloxidolor : EPAR - Summary for the public LT = lietuvių kalba 2013-05-13  
Meloxidolor : EPAR - Summary for the public HU = magyar 2013-05-13  
Meloxidolor : EPAR - Summary for the public MT = Malti 2013-05-13  
Meloxidolor : EPAR - Summary for the public NL = Nederlands 2013-05-13  
Meloxidolor : EPAR - Summary for the public PL = polski 2013-05-13  
Meloxidolor : EPAR - Summary for the public PT = português 2013-05-13  
Meloxidolor : EPAR - Summary for the public RO = română 2013-05-13  
Meloxidolor : EPAR - Summary for the public SK = slovenčina 2013-05-13  
Meloxidolor : EPAR - Summary for the public SL = slovenščina 2013-05-13  
Meloxidolor : EPAR - Summary for the public FI = suomi 2013-05-13  
Meloxidolor : EPAR - Summary for the public SV = svenska 2013-05-13  

This EPAR was last updated on 15/03/2016 .

Authorisation details

Product details

Product details for Meloxidolor
NameMeloxidolor
Agency product numberEMEA/V/C/002590
Active substance

meloxicam

International non-proprietary name (INN) or common name

meloxicam

Species HorsesDogsPigsCatsCattle
Anatomical therapeutic chemical veterinary (ATCvet) codeQM01AC06
Generic

A generic medicine is a medicine which is similar to a medicine that has already been authorised (the 'reference medicine'). A generic medicine contains the same quantity of active substance(s) as the reference medicine. Generic and reference medicines are used at the same dose to treat the same disease, and they are equally safe and effective.

Publication details

Publication details for Meloxidolor
Marketing-authorisation holder

Le Vet Beheer B.V

Revision5
Date of issue of marketing authorisation valid throughout the European Union22/04/2013

Contact address:

Le Vet Beheer B.V
Wilgenweg 7
3421 TV Oudewater
The Netherlands

Product information

Product information

05/02/2016  Meloxidolor -EMEA/V/C/002590 -IAIN/0006

Name Language First published Last updated
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - Product Information SV = svenska 2013-05-13 2016-03-15

Contents

  • Annex I - Summary of product characteristics
  • Annex IIA - Manufacturing-authorisation holder responsible for batch release
  • Annex IIB - Conditions of the marketing authorisation
  • Annex IIIA - Labelling
  • Annex IIIB - Package leaflet

Please note that the size of the above document can exceed 50 pages.

You are therefore advised to be selective about which sections or pages you wish to print.


Name Language First published Last updated
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15
Meloxidolor : EPAR - All Authorised presentations SV = svenska 2013-05-13 2016-03-15

Pharmacotherapeutic group

Anti-inflammatory and antirheumatic products, non-steroids (oxicams)

Therapeutic indication

Dogs

  • Alleviation of inflammation and pain in both acute and chronic musculoskeletal disorders.
  • Reduction of postoperative pain and inflammation following orthopaedic and soft-tissue surgery.

Cats

  • Reduction of postoperative pain after ovariohysterectomy and minor soft-tissue surgery.

Cattle

  • For use in acute respiratory infection with appropriate antibiotic therapy to reduce clinical signs.
  • 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 noninfectious locomotor disorders to reduce the symptoms of lameness and inflammation.
  • For the relief of postoperative pain associated with minor soft-tissue surgery such as castration.
  • 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.

Assessment History

Changes since initial authorisation of medicine

Name Language First published Last updated
Meloxidolor : EPAR - Procedural steps taken and scientific information after authorisation SV = svenska 2013-12-04 2016-03-15

Initial marketing-authorisation documents

Name Language First published Last updated
Meloxidolor : EPAR - Public assessment report SV = svenska 2013-05-13  
CVMP summary of positive opinion for Meloxidolor SV = svenska 2013-02-08  

Authorised

This medicine is approved for use in the European Union

More information on Meloxidolor