Report side effects of Neulasta

NEULASTA®(PEGFILGRASTIM) PATIENT SIDE EFFECT REPORTING

If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in the patient 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.
If you think there may be a defect or quality issue with the Amgen product you have received, please call us on +44 (0) 1223 436441 or Freephone 1800 535 160 and provide 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 side effects please see the Patient Information Leaflet (PIL).

This site is intended for patients in Ireland who are being treated with an Amgen® product and for Irish Healthcare Professionals (HCPs).

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IE-CBU-0820-00002 August 2020