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AMGEN SUPPORT MATERIALS AND PROGRAMMES FOR YOU AND YOUR PATIENTS

Amgen's mission is to serve patients. We are committed to providing you and your patients with the support you need

Patient journeys can be diverse. Amgen understands this and provides a host of services to support you, your care team, and your patients.

Amgen has developed a robust patient education and support programme to help patients throughout their course of treatment, ensuring informed dialogues with you as their physician and that the best possible outcomes are achieved.

Amgen's patient education materials are available as a supportive tool to help provide patients with the information they need throughout their treatment.

Resources for HCPs

AMGEVITA^® Summary of Product Characteristics

Amgevita^® SmPC

Publications

Rheumatoid arthritis clinical bioequivalence publication

Plaque psoriasis clinical bioequivalence publication

Open-label extension study in rheumatoid arthritis publication

AMGEVITA^® Package Leaflet

AMGEVITA^® package leaflet

Device Training Resources

SmPC

AMGEVITA^® is authorised for the following indications by the European Commission:
AMGEVITA^® is an adalimumab biosimilar indicated for the treatment of rheumatoid arthritis, juvenile idiopathic arthritis, axial spondyloarthritis, psoriatic arthritis, psoriasis, paediatric plaque psoriasis, hidradenitis suppurativa, Crohn’s disease, paediatric Crohn’s disease, ulcerative colitis, uveitis and paediatric uveitis.

AMGEVITA^® (adalimumab) Summary of Product Characteristics. Available at: www.ema.europa.eu. Last revised March 2020.

▼ This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions.

The information contained in this website is for European healthcare professionals only

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▼This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions.