Rheumocam
Active substance
ATC code
Species
Horses.
Indications
Alleviation of inflammation and pain in both acute and chronic musculo-skeletal disorders in horses.
Dose to be administered and administration route
To be administered either mixed with food or directly into the mouth at a dosage of 0.6 mg/kg body weight, once daily, up to 14 days. In case the veterinary medicinal product is mixed with food, it should be added to a small quantity of food, prior to feeding.
The suspension should be given using the Rheumocam measuring syringe provided in the package. The syringe fits onto the bottle and has a 2 ml scale.
Shake well before use.
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.
Adverse reactions
Horses:
Very rare (<1 animal / 10,000 animals treated, including isolated reports): |
Appetite loss, Lethargy Diarrhoea1, Abdominal pain, colitis Urticaria1,2, Anaphylactoid reaction3 |
1Reversible
2Slight
3May be serious (including fatal). If such a 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.
Dispensing
POM-V - Prescription Only Medicine – Veterinarian
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Art. Nr. | 08749/5020 |