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Please note that RYDAPT®▼ (midostaurin) is not subject to additional monitoring in Northern Ireland.

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UK | September 2023 | 307240

Please note that RYDAPT®▼ (midostaurin) is not subject to additional monitoring in Northern Ireland.

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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.novartis.com/report
If you have a question about the product, please contact Medical Information on 01276 698370 or by email at [email protected]