Rycarfa 50mg/ml Injection 20ml
Krka Uk
Rycarfa 50mg/ml Injection 20ml from KRKA UK LTD is supplied as a solution for injection.
LEGAL CLASSIFICATION:POM-V
THIS MEDICINE REQUIRES A PRESCRIPTION.
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Cold-chain product: dispatched at 2–8°C in insulated packaging. Please refrigerate on arrival; do not freeze.
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A link to the Medicine SPC on the VMD Product database can be found here: VMD Product Database
UK Public Assessment Report: UKPAR (PDF)
Post-Authorisation Assessment Report: PAAR (PDF)
Read the full Rycarfa product information ›
Active Ingredient(s)
Carprofen
Pack & Presentation
Form: Solution for injection · Pack size: 20ML
Suitable Species
Cats, Dogs
Owner Handling & Safety
Care should be taken to avoid accidental self-injection. Carprofen, in common with other NSAIDs, has been shown to exhibit photosensitising potential in laboratory animals. Avoid skin contact with the veterinary medicinal product.
Regulatory Information
- Legal category: POM-V
- Marketing authorisation holder: KRKA, d.d., Novo mesto Šmarješka cesta 6 8501 Novo mesto Slovenia Further information Pharmacotherapeutic group: Antiinflammatory and antirheumatic products, nonsteroids. ATCvet code: QM01AE91 Carprofen possesses anti-inflammatory, analgesic and antipyretic activity. Like most other NSAID’s, carprofen is an inhibitor of the enzyme cyclo-oxygenase of the arachidonic acid cascade. However, the inhibition of prostaglandin synthesis by carprofen is slight in relation to its anti-inflammatory and analgesic potency. The precise mode of action of carprofen is not clear. Carprofen is a chiral drug with the S(+) enantiomer being more active than the R(-) enantiomer. There is no chiral inversion between the enantiomers in-vivo. Carprofen is well absorbed after subcutaneous administration with peak plasma concentrations achieved within 3 h after administration. The volume of distribution is small. Carprofen is highly protein bound. Carprofen is characterized by a half-life of approximately 10 hours in dogs. In cats, the elimination half-life is longer ranging from 9-49 hours after intravenous administration (mean of 20 hrs). Special precautions for the disposal of unused veterinary medicinal products or waste materials derived from the use of such products: Medicines should not be disposed of via wastewater. Use take-back schemes for the disposal of any unused veterinary medicinal product or waste materials derived thereof in accordance with local requirements and with any national collection systems applicable to the veterinary medicinal product concerned. List of Excipients: Benzyl alcohol (E1519) (10 mg), Arginine Glycocholic acid, Hydrochloric acid dilute (for pH adjustment), Lecithin, Sodium hydroxide, Water for injections
- MA number: Vm 01656/4174
Important Notice
The information on this page is provided for general guidance only and does not replace the advice of a qualified veterinary surgeon. Always follow the directions provided on the product packaging and by your veterinary practice. If your animal's condition does not improve, worsens, or any side effects occur, contact your veterinary surgeon immediately.




