1. Medicines
  2. Rheumatology
  3. COSENTYX® (secukinumab)
  4. UnoReady® 300mg pen

Click here for Prescribing Information

UnoReady® 300mg pen

UnoReady® 300mg pen

All the benefits of Cosentyx 300mg now available in ONE 300mg UnoReady® pen1

Image. UNOREADY® 300mg PEN key feature

300 mg autoinjector pen with call-out benefits

 

 

UnoReady® 300mg pen:
Similar administration steps as the SensoReady® 150mg pen, with a few differences.5

 

300 mg autoinjector pen with a list of key features
150 mg autoinjector pen with a list of key features
 
 

The Cosentyx® SensoReady® 150 mg pen will remain available, giving you the option to choose a dose based on your patients’ needs.
If you would like to order a demo-kit or for further information on the UnoReady® 300mg pen, please contact your Novartis Representative.

*Individual patient dosing may vary - please consult the Prescribing Information for full details. Psoriatic Arthritis: Recommended dose is 300mg in patients with concomitant moderate to severe plaque psoriasis or who are anti-TNFα inadequate responders. For other patients, the recommended dose is 150mg. Based on clinical response, the dose can be increased to 300mg. Ankylosing Spondylitis: Recommended dose is 150mg. Based on clinical response, the dose can be increased to 300mg. response. Non-radiographic axial spondyloarthritis: Recommended dose is 150mg.
†N=37, moderate-to-severe plaque psoriasis patients at Week 28.2
‡In a clinical study, adverse events with the preferred term injection-site bruising or injection-site pain due to administration of Cosentyx using the UnoReady® pen over 52 weeks.

DMARD, disease-modifying anti-rheumatic drugs; MTX, methotrexate; NSAIDs, non-steroidal anti-inflammatory drugs; PsA, psoriatic arthritis.

References

  1. Cosentyx Summary of Product Characteristics. Available at www.medicines.ie. Accessed November 2024.
  2. Novartis data on file. CAIN457A2325 Data Analysis Report. Satisfaction with self-injection. December 2020.
  3. Novartis data on file. CAIN457A2325 Data Analysis Report. Injection site reaction rate. December 2020.
  4. Cosentyx 300mg Patient Leaflet. Available at www.medicines.ie. Accessed March 2023.
  5. Paul C et al. J Eur Acad Dermatol Venereol. 2015;29(6):1082-1090.
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IE271483-1 | November 2024
Rheumatology
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Reporting of side effects
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.