PERMISSION TO CALL PATIENT
Submit this form and a dedicated Altogether You nurse will be in touch with your patient.
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Tailored support for your patients
Regular contact with a dedicated nurse
- Regular contact with a nurse.
- Offer individualised education and coaching around their condition, treatment and personal health goals, such as diet and quitting smoking.
Reminders
- Patients are offered optional dose reminders, via email/SMS or both.
- New patients will also receive a reminder notification at 12 weeks after commencing treatment to make an appointment with their healthcare professional and complete pathology (if required) to continue with Cosentyx.
Device training
- Access to ongoing device training and education.
Contact
Contact Altogether You Program Support on: 1800 023 826
Privacy and Patient Safety Statement
By providing your personal information to Novartis Pharmaceuticals Australia Pty Ltd or its related bodies corporate (Novartis), you consent to Novartis collecting, storing and using your personal information in accordance with the Novartis Privacy Policy at https://www.novartis.com.au/privacy-policy. In particular, you consent to Novartis using your personal information to communicate with you about Novartis products and/or to support your use of those products, and you consent to Novartis using your personal information for audit or inspection purposes. Novartis reserves the right to use aggregated and de-identified data collected through this Activity. You also consent to Novartis using your personal information to (where applicable) invite you to, or arrange your participation in, activities managed by (or on behalf of) Novartis.
Novartis has engaged third party service providers (Approved Contractors) for the purposes of administering the Altogether You Support Program (Activity). Approved Contractors, for the purposes of the Activity, may include Medical Safety Systems Corporate Pty Ltd trading as RxMx Australia (RxMx). You consent to the Approved Contractor(s) collecting, storing and using your personal information in connection with the Activity, including to organise your participation in the Activity or to communicate with you in relation to the Activity, in accordance with the Novartis Privacy Policy.
Novartis is committed to patient safety. In accordance with regulatory obligations for reporting safety information Novartis processes reports of adverse events experienced by patients on Novartis products when identified by a Novartis representative (or by a third party acting on behalf of Novartis). Novartis Patient Safety may contact you or your healthcare professional in order to collect further information on the adverse event. This information may be shared with health authorities or other pharmaceutical companies with whom Novartis has a license agreement, and third parties we work with for the purpose of safety reporting.
Your information may be stored on servers located in jurisdiction outside of Australia. Some of those countries may not offer the same level of privacy protection as in Australia. However, Novartis will enter into agreements with its third party service providers to keep your information secure and provide adequate protection for your data.
You are not obliged to provide personal information. However, if you do not provide information you may not, for example, be able to participate fully in activities managed by us.
You have the right to access, update or correct your personal information and/or decline to receive communications from Novartis. To find out how, please refer to https://www.novartis.com.au/privacy-policy or contact our Privacy Officer at Novartis Australia, Phone: 02 9805 3555, Email: privacy.au@novartis.com.
Adverse events: Very common (≥10%) nasopharyngitis. Common (≥1 to <10%): upper respiratory tract infection, rhinitis, pharyngitis, oral herpes, diarrhoea, urticaria, dermatitis (including eczema), rhinorrhoea, headache, nausea, hypercholesterolemia.
PBS Information: Section 85 Authority Required for the treatment of severe chronic plaque psoriasis, active ankylosing spondylitis, severe psoriatic arthritis, non-radiographic axial spondyloarthritis and hidradenitis suppurativa. Refer to PBS Schedule for full Authority information.
This medicinal product is subject to additional monitoring in Australia due to approval of an extension of indications. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse events at www.tga.gov.au/reporting-problems.
Novartis encourages healthcare professionals and consumers to report any adverse events associated with our products. You can also report side effects to the Novartis Drug Safety on 1800 671 203.
For healthcare professionals only. Please review full Product Information before prescribing.
Scan QR Code for full Cosentyx product information. Alternatively, please contact med info at 1800 671 203 or visit www.novartis.com.au/products/healthcare-professionals/products to access the full product information.
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Novartis Pharmaceuticals Australia Pty Limited. ABN 18 004 244 160. Sydney NSW. Ph +61 2 9805 3555. Date of prepartion: March 2026. AU-30162. RxPx.