PRODUCTS

At Amgen, our mission is to serve patients. We are proud to have made an impact on the lives of millions with our medicines.

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Products

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.

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 (UK and Ireland), Freephone: 1800 535160 (Ireland) and provide us with the details:

  • You think you may have experienced an adverse event ('side effect') 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.

If you are in the UK (England, Scotland, Wales and Northern Ireland), you can also report side effects or product defects directly to the  Medicines and Healthcare products Regulatory Agency (MHRA).  

If you are in Ireland, you may also report side effects or product defects to the  Health Products Regulatory Authority (HPRA) where you can also find reporting forms and information.

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

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

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 Electronic Medicines Compendium (eMC) and Medicines.ie websites; and provide information about all medicines available in United Kingdom and Ireland respectively.

Please note that this information is specific to United Kingdom and Ireland. Click here to read our Terms and Conditions of Sale.

A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z

Neulasta® (pegfilgrastim)

Neulasta® - United Kingdom Summary of Product Characteristics and Patient Information Leaflet

Neulasta® - Ireland Summary of Product Characteristics and Patient Information Leaflet

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Nplate® (romiplostim) 

Nplate® - United Kingdom Summary of Product Characteristics and Patient Information Leaflet

Nplate® - Ireland Summary of Product Characteristics and Patient Information Leaflet

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Prolia® (denosumab)

Prolia® - United Kingdom Summary of Product Characteristics and Patient Information Leaflet

Prolia® - Ireland Summary of Product Characteristics and Patient Information Leaflet

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Total of 18 Products

Amgen is committed to patient safety and continually monitors the safety and quality of our products. Side effects and product quality issues should be reported.

▼This product is subject to additional monitoring, which will allow quick identification of new safety information. You can help by reporting any side effects you may get by using the links below.

For the UK - reporting forms and information can be found at http://yellowcard.mhra.gov.uk/

For Ireland - reporting forms and information can be found at http://www.hpra.ie/

Side effects and product quality issues should also be reported to Amgen. To report a potential adverse event or quality issue with an Amgen product, or for medical information enquiries, please call +44 (0) 1223 436441 (UK and Ireland) or Freephone: 1800 535160 (Ireland).

Job Code: GBR-NP-1224-80003

Date of preparation: January 2025