Kyprolis

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Kyprolis^® (carfilzomib) -
information for patients

This site is designed to provide patients who have been prescribed Kyprolis^® (carfilzomib) with information about their treatment and other useful materials. Should you have any concerns or questions regarding your treatment with Kyprolis^®, please speak to your doctor, pharmacist or nurse.

Downloadable resources

Downloadable patient resources

Click the links below to read or download useful materials to help support you.

patient-resources1

Kyprolis^®(carfilzomib) treatment cycle tracker

To help you record details
of your treatment

Download (PDF)

patient-resources2

Treatment with Kyprolis^® (carfilzomib)
for myeloma - a Patient's Guide

Patient booklet

Read More
Download (PDF)

If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in the package leaflet. Side effects can be reported directly to the Health Products Regulatory Authority (HPRA) using the available methods via www.hpra.ie. By reporting side effects you can help provide more information on the safety of this medicine. Side effects should also be reported to Amgen Limited on +44 (0) 1223 436441 or Freephone 1800 535 160.

Please report any potential quality issue with the Amgen product you have received, by calling us on +44 (0) 1223 436441 or Freephone 1800 535 160 and providing us with the details. Please ensure that you keep your packaging, so we are able to identify your product more easily.

For a list of possible side effects, please see

Patient Information Leaflet (PIL)