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Reporting Adverse Events

Repatha^® (evolocumab) is subject to additional monitoring. Adverse events should be reported. Reporting forms and information can be found:

www.mhra.gov.uk/yellowcard

Adverse events should also be reported to Amgen Limited on:

+44 (0) 1223 436 441

If you think there may be a defect or quality issue with the Amgen product you have received, please provide us with the details via phone call:

+44 (0) 1223 436 441

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