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The website to which you will be redirected may be designed exclusively for residents of a particular country or countries, as advertised on that website. As a consequence, the website to which you will be directed may contain information on pharmaceutical products or indications that are not approved in Europe. If You reside in a country other than the one to which such website is directed, please contact your local Amgen affiliate for the correct information on products in your country of residence.

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At Amgen, our mission is to serve patients. As a science-based, patient-focused organisation, we discover and develop innovative therapies to treat serious illnesses. Our medicines have made a difference in the lives of millions.

Amgen is committed to patient safety and continually monitors the safety and quality of our products. If you want to contact Amgen for any of the following reasons, please call us on +44 (0)1223 436441 or Freephone: 1800 535160, and provide us with the details:

  • You think you may have experienced a side effect (‘adverse event’) after taking or using an Amgen product.
  • You think there may be a defect or quality issue with the Amgen product you have received.
  • You have a general medical information enquiry about your Amgen product.

If you do have any side effects, talk to your healthcare professional. This includes any possible side effects not listed in the package leaflet.

You may also report adverse events or product defects to the Health Products Regulatory Authority (HPRA) where you will find reporting forms and information.

To read more about the Falsified Medicines Directive and the impact this may have on Amgen packaging, click here.

Below you will find information on Amgen’s product portfolio. Summary of Product Characteristics and patient information leaflets for each product can be accessed via the links. These links direct you to the Medicines.ie website; and provide information about all medicines available in Ireland.

By reporting side effects, you can help provide more information on the safety of our medicines.

▼This product is subject to additional monitoring, which will allow quick identification of new safety information.

Reporting forms and information can be found at http://www.hpra.ie/



Job Code: IRL-NP-1124-80010
Date of preparation: December 2024