Prescribing information

 

Cosentyx is indicated for the treatment of: moderate to severe plaque psoriasis in adults who are candidates for systemic therapy; active psoriatic arthritis in adult patients, alone or in combination with MTX, when the response to previous DMARD therapy has been inadequate; active ankylosing spondylitis in adults who have responded inadequately to conventional therapy; active non-radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated CRP and/or MRI evidence in adults who have responded inadequately to NSAIDs.

Explore our resources designed to support Cosentyx initiation and ongoing maintenance for patients with plaque psoriasis.

You can download certain files below for you to share with your Cosentyx patients separately. Do not share links to this website or screenshots with patients as this website is intended for healthcare professionals only.

Please note that these resources are designed for optimal use on desktop or tablet. Functionality may be restricted on some devices, including mobile.

 

Image of Cosentyx digital patient pack

Digital patient pack

This interactive PDF contains everything your patients need to get going with treatment and to help them get the most out of it.

Download

Cosentyx® (secukinumab) patient resources

Digital patient leaflet

This condensed PDF summary of the patient pack will introduce your patients to Cosentyx.

Download

Image of Cosentyx digital patient leaflet

Digital dosing schedule

​An interactive PDF to help your newly initiated Cosentyx patients keep track of their treatment.

View

 

Image of Cosentyx digital dosing schedule

SensoReady® injection video

A short instructional video that demonstrates how to prepare and deliver Cosentyx injections.

See more

 

CRP, C-reactive protein; DMARD, disease-modifying anti-rheumatic drug; MRI, magnetic resonance imaging; MTX, methotrexate; NSAIDs, non-steroidal anti-inflammatory drugs.

UK | March 2021 | 104092
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Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard. Adverse events should also be reported to Novartis via [email protected] or online through the pharmacovigilance intake (PVI) tool at www.report.novartis.com
If you have a question about the product, please contact Medical Information on 01276 698370 or by email at [email protected]