Loxicom 0.5 mg/ml Oral Suspension for Dogs
Active ingredient: Meloxicam
Form
Liquid
Species
Manufacturer
Norbrook Laboratories Limited
VMD MA No.
02000/5001
What it's used for
Alleviation of inflammation and pain in both acute and chronic musculo-skeletal disorders in dogs.
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Prescription required
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Loxicom 0.5 mg/ml Oral Suspension for Dogs — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 26 Mar 2026.
disorders in dogs.
Initial treatment is a single dose of 0.2 mg meloxicam/kg bodyweight (i.e. 4 ml/10 kg
bodyweight) on the first day. Treatment is to be continued once daily by oral
administration (at 24 hour intervals) at a maintenance dose of 0.1 mg meloxicam/kg
bodyweight (i.e. 2 ml/10 kg bodyweight).
For longer term treatment, once clinical response has been observed (after ≥ 4
days), the dose can be adjusted to the lowest effective individual dose reflecting that
the degree of pain and inflammation associated with chronic musculo-skeletal
disorders may vary over time.
Particular care should be taken with regard to the accuracy of dosing.
The suspension can be given using either of the two measuring syringes provided in
the package. The syringes fit onto the bottle and have a kg-bodyweight scale which
corresponds to the maintenance dose (i.e. 0.1 mg meloxicam/kg bodyweight). Thus
for the first day, twice the maintenance volume will be required. Alternatively therapy
may be initiated with Loxicom 5 mg/ml solution for injection.
A clinical response is normally seen within 3-4 days. Treatment should be
discontinued after 10 days at the latest if no clinical improvement is apparent.
Advice on correct administration
To be administered with food or directly into the mouth.
Shake well before use.
Avoid introduction of contamination during use.
Do not use in dogs suffering from gastrointestinal disorders such as irritation and
haemorrhage, impaired hepatic, cardiac or renal function and haemorrhagic
disorders.
Do not use in case of hypersensitivity to the active substance or to any of the
excipients.
Do not use in dogs less than 6 weeks of age.
Issued: November 2024
AN: 01004/2024
faecal occult blood, apathy and renal failure have occasionally been reported . In
very rare cases, haemorrhagic diarrhoea, haematemesis, gastrointestinal ulceration
and elevated liver enzymes have been reported.
These adverse reactions occur generally within the first treatment week and are in
most cases transient and disappear following termination of the treatment but in very
rare cases may be serious or fatal.
If adverse reactions occur, treatment should be discontinued and the advice of a
veterinarian should be sought.
The frequency of adverse reactions is defined using the following convention:
- very common (more than 1 in 10 animals treated displaying adverse reactions)
- 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
If adverse reactions 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 is a
potential risk of renal toxicity.
This product for dogs should not be used in cats due to the different dosing devices.
In cats, Loxicom 0.5 mg/ml oral suspension for cats should be used.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals
People with known hypersensitivity to non-steroidal anti-inflammatory drugs
(NSAIDs) should avoid contact with the veterinary medicinal product.
In case of accidental ingestion, seek medical advice immediately and show the
package leaflet or the label to the physician.
This product can cause eye irritation. In case of contact with the eyes, immediately
rinse thoroughly with water.
with high protein binding may compete for binding and thus lead to toxic effects.
Loxicom must not be administered in conjunction with other NSAIDs or
glucocorticosteroids.
Pre-treatment with other anti-inflammatory substances may result in additional or
increased adverse effects and accordingly a treatment-free period with such
veterinary medicinal products should be observed for at least 24 hours before
commencement of treatment. The treatment-free period, however, should take into
account the pharmacological properties of the products used previously.
Issued: November 2024
AN: 01004/2024
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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Related Conditions
Other Products Containing Meloxicam
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
Animeloxan 1.5 mg/ml Oral Suspension for Dogs
POM-VaniMedica GmbH
Animeloxan 1.5 mg/ml Oral Suspension for Dogs
POM-VaniMedica GmbH
Animeloxan 20 mg/ml Solution for Injection for Cattle, Pigs and Horses
POM-VaniMedica GmbH
Animeloxan 5 mg/ml Solution for Injection for Dogs and Cats
POM-VaniMedica GmbH
Arthrocam 0.5 mg/ml Oral Suspension for Cats
POM-VChanelle Pharmaceuticals Manufacturing Ltd
Arthrocam 0.5 mg/ml Oral Suspension for Cats
POM-VChanelle Pharmaceuticals Manufacturing Ltd
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