You are now leaving Amgen's website www.amgencare.ie and entering another website. Amgen is not responsible for the content of this third-party website you are entering now and is not adopting such content into this website. If you want to leave www.amgencare.ie please click continue:

Return to Previous Page Continue

Vectibix^® (panitumumab) - information for patients

This site is designed to provide adult patients who have been prescribed Vectibix^® (panitumumab) with information about their treatment and other useful materials. Should you have any concerns or questions regarding your treatment with Vectibix^®, 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.

A guide for patients prescribed Vectibix (Panitumumab)

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)

Downloadable patient resources

Reporting of side effects: