Inflacam 5 mg/ml Solution for Injection for Dogs and Cats
Active ingredient: Meloxicam
Form
Injection
Species
Manufacturer
Chanelle Pharmaceuticals Manufacturing Ltd
VMD MA No.
08749/5015
What it's used for
and soft tissue surgery. Cats Reduction of post-operative pain after ovariohysterectomy and minor soft tissue surgery.
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Paying less for Meloxicam
-
1
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2
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Prescription required
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Inflacam 5 mg/ml Solution for Injection for Dogs and Cats — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.
Cats
Reduction of post-operative pain after ovariohysterectomy and minor soft tissue
surgery.
Dogs
Musculo-skeletal disorders:
Single subcutaneous injection at a dosage of 0.2 mg meloxicam/kg body weight (i.e.
0.4 ml/10 kg body weight).
Inflacam 1.5 mg/ml oral suspension for dogs or Inflacam 1 mg and 2.5 mg chewable
tablets for dogs may be used for continuation of treatment at a dosage of 0.1 mg
meloxicam/kg body weight, 24 hours after administration of the injection.
Reduction of post-operative pain (over a period of 24 hours):
Single intravenous or subcutaneous injection at a dosage of 0.2 mg meloxicam/kg
body weight (i.e. 0.4 ml/10 kg body weight) before surgery, for example at the time of
induction of anaesthesia.
Cats
Reduction of post-operative pain:
Single subcutaneous injection at a dosage of 0.3 mg meloxicam/kg body weight (i.e.
0.06 ml/kg body weight) before surgery, for example at the time of induction of
anaesthesia.
To ensure a correct dosage, body weight should be determined as accurately as
possible.
The use of suitably calibrated measuring equipment is recommended.
Avoid introduction of contamination during use.
Maximum number of piercings is 42 for all presentations.
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 animals less than 6 weeks of age nor in cats of less than 2 kg.
Refer to section 3.7.
Very rare
(<1 animal / 10,000 animals
treated, including isolated
reports):
Appetite loss, Lethargy
Vomiting, Diarrhoea, Blood in faeces
,
Haemorrhagic diarrhoea
, Haematemesis
,
Gastric ulcer
, Small intestine ulcer
, Large
intestine ulcer
Elevated liver enzymes
Renal failure
Anaphylactoid reaction
1
Occult
These side effects 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 such reaction occurs, it should be treated symptomatically.
If adverse reactions occur, treatment should be discontinued and the advice of a
veterinarian should be sought.
Reporting adverse events is important. It allows continuous safety monitoring of a
veterinary medicinal product. Reports should be sent, preferably via a veterinarian, to
either the marketing authorisation holder or its local representative or the national
competent authority via the national reporting system. See also the package leaflet for
respective contact details.
Special precautions for safe use in the target species:
Avoid use in any dehydrated, hypovolaemic or hypotensive animal, as there is a
potential risk of renal toxicity.
During anaesthesia, monitoring and fluid therapy should be considered as standard
practice.
Any oral follow-up therapy using meloxicam or other NSAIDs should not be
administered in cats, as appropriate dosage regimens for such follow-up treatments
have not been established.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals:
Accidental self-injection may give rise to pain.
People with known hypersensitivity to non-steroidal anti-inflammatory drugs (NSAIDs)
should avoid contact with the veterinary medicinal product.
In case of accidental self-injection, seek medical advice immediately and show the
package leaflet or the label to the physician.
Special precautions for the protection of the environment:
Not applicable.
with high protein binding may compete for binding and thus lead to toxic effects. The
veterinary medicinal product must not be administered in conjunction with other
NSAIDs or glucocorticosteroids. Concurrent administration of potential nephrotoxic
drugs should be avoided. In animals at anaesthetic risk (e.g. aged animals)
intravenous or subcutaneous fluid therapy during anaesthesia should be taken into
consideration. When anaesthesia and NSAID are concomitantly administered, a risk
for renal function cannot be excluded.
Pre-treatment with 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 should however take into account the pharmacological
properties of the veterinary medicinal products previously used.
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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