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Why Cosentyx in axSpA?

Dive into the data below to see how Cosentyx could help your patients with axSpA

Cosentyx_AxSpA_HCP

 

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  1. Cosentyx (secukinumab) Summary of Product Characteristics. Available at www.medicines.ie. Accessed March 2023
  2. Marzo-Ortega H et al. Arthritis Rheumatol. 2019;71(suppl 10). Abstract 1504.
  3. Baraliakos X et al. RMD Open. 2019;5(2):e001005.
  4. Baeten D et al. N Engl J Med. 2015;373(26):2534-2548.
  5. Novartis data on file. CAIN457F2310 Data Analysis Report. June 2019.
  6. Novartis data on file. CAIN457F2310 (MEASURE 2): Nocturnal Back Pain. January 2020.
  7. Marzo-Ortega H et al. Arthritis Care Res. 2017;69(7):1020-1029 and Supplementary Tables.
  8. Deodhar A et al. Clin Exp Rheumatol. 2019;37(2):260-269.
  9. Taurog JD et al. N Engl J Med. 2016; 375(13):1303.
  10. Zochling J. Arthritis Care Res (Hoboken). 2011;63(suppl 11):S47-S58.
  11. Novartis data on file. CAIN457F2310 (MEASURE 2): Nocturnal Back Pain. February 2021.
  12. Zochling J. Arthritis Care Res (Hoboken). 2011;63(suppl 11):S47-S58.
  13. Braun J et al. Rheumatology (Oxford). 2019;58(5):859-868.
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IE271483 | March 2023

Reporting of side effects
Reporting suspected adverse reactions of the medicinal product is important to Novartis and the HPRA. It allows continued monitoring of the benefit/risk profile of the medicinal product. All suspected adverse reactions should be reported via HPRA Pharmacovigilance, website: www.hpra.ie. Adverse events could also be reported to Novartis preferably via www.report.novartis.com or by email: [email protected] or by calling 01 2080 612.

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