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Cosentyx® (secukinumab): Resources

Cosentyx is indicated for the treatment of moderate to severe plaque psoriasis (PsO) in adults, children and adolescents from the age of 6 years who are candidates for systemic therapy; active psoriatic arthritis (PsA) in adult patients (alone or in combination with methotrexate [MTX]) when the response to previous disease-modifying anti-rheumatic drug therapy has been inadequate; active ankylosing spondylitis (AS) in adults who have responded inadequately to conventional therapy; active non-radiographic axial spondyloarthritis (nr-axSpA) with objective signs of inflammation as indicated by elevated C-reactive protein and/or magnetic resonance imaging evidence in adults who have responded inadequately to non-steroidal anti-inflammatory drugs; active moderate to severe hidradenitis suppurativa (HS; acne inversa) in adults with an inadequate response to conventional systemic HS therapy; active enthesitis-related arthritis (ERA) in patients 6 years and older (alone or in combination with MTX) whose disease has responded inadequately to, or who cannot tolerate, conventional therapy; active juvenile psoriatic arthritis (JPsA) in patients 6 years and older (alone or in combination with MTX) whose disease has responded inadequately to, or who cannot tolerate, conventional therapy.1

Cosentyx is intended for use under the guidance and supervision of a physician experienced in the diagnosis and treatment of conditions for which Cosentyx is indicated.1 

In Ireland Cosentyx is reimbursed for the following indications: adult plaque psoriasis (PsO); psoriatic arthritis (PsA) and axial spondyloarthritis (axSpA).

Information on the Cosentyx safety profile may be found on the safety profile page of this website and the Cosentyx Summary of Product Characteristics (SmPC).1


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

Below you can download helpful resources that you can share with your Cosentyx patients. Do not share links to this website or screenshots with patients as this website is intended for healthcare professionals (HCPs) only.

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

Please do not share links to this page with patients.
This section of the website is intended for HCPs only. If you wish to direct patients to the patient resources, use the link below:
https://cosentyx-patientinformation.ie/

SensoReady® 150 mg injection video

A short instructional video that demonstrates how to prepare and inject Cosentyx with the SensoReady® 150 mg pen.

UnoReady® 300 mg injection video

A short video showing you how to prepare and inject Cosentyx with the UnoReady® 300 mg pen.

Dosing guide

Self-injection guide

My medication pass

About psoriasis

Welcome booklet

Travel letter

Travel pass



AS, ankylosing spondylitis; axSpA, axial spondyloarthritis; ERA; enthesitis-related arthritis; HCP, healthcare professional; HS, hidradenitis suppurativa; JPsA, juvenile psoriatic arthritis; MTX, methotrexate; nr-axSpA, non-radiographic axial spondyloarthritis; PsA, psoriatic arthritis; PsO, plaque psoriasis; SmPC, summary of product characteristics.

Reference

  1. Cosentyx® (secukinumab) Summary of Product Characteristics. Available at www.medicines.ie.

IE11485243 | April 2026

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk profile of the medicinal product. All suspected adverse reactions should be reported to HPRA Pharmacovigilance at www.hpra.ie. Adverse events can also be reported to Novartis preferably at www.novartis.com/report, by emailing [email protected] or by calling (01) 2080 612.