Legal Class: Class III Medical Device

Active Substances: Sodium Hyaluronate 1.6% – 800mg/50ml, and Sodium Chondroitin Sulfate 2% – 1g/50ml and calcium chloride (0.87% – 440mg/50ml)

Each box of iAluRil contains the following items.

  • Prefilled syringe with 50ml of iAluRil (1)
  • Plunger to be screwed into the end of the syringe (2)
  • Luer-lock adapter for securing to an intermittent catheter (3)
  • iAluAdapter to enable catheter free instillation of iAluRil (4)

Essential Information
iAluRil Prefill for intravesical instillation Indication: To re-establish the glycosaminoglycan layers (GAGs) of the urothelial vesical tissue in cases in which their loss can cause frequent and recurring problems (such as, cystitis of varying etiology). Active Ingredients: Sodium hyaluronate (1.6%), Sodium chondroitin sulphate (2%) and Calcium chloride (0.87%). Please read the full patient information leaflet for further information and before administration. iAluRil should only be used after careful consultation with a trained healthcare professional.
Reporting of Side Effects
If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in the product’s package leaflet. You can also report side effects directly via the Yellow Card Scheme at www.mhra.gov.uk/yellowcard. By reporting side effects you can help provide more information on the safety of this medical device.
Revision reference –iAluRil_13_21.10.2020