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Adverse events should be reported to the Medicines and Healthcare products Regulatory Agency.
Reporting forms and information can be found at: www.mhra.gov.uk/yellowcard
Adverse events should also be reported to Takeda at AE.GBR-IRL@takeda.com

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Site last update: May 2023. Main website content job code: C-ANPROM/EUC/NBU/0201

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