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European Regional Headquarters

Amgen (Europe) GmbH
Suurstoffi 22,
CH-6343 Rotkreuz,
Switzerland
Phone: +41 41 3690 300
Fax: +41 41 3690 400

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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.

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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.