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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 online through the pharmacovigilance intake (PVI) tool at www.novartis.com/report, or alternatively email [email protected] or call 01276 698370.
 
 
 
 
 
 
 
 
 
![Lutathera® (lutetium [177Lu] oxodotreotide) logo Lutathera® (lutetium [177Lu] oxodotreotide) logo](https://www.pro.novartis.com/uk-en/sites/pro_novartis_com_uk/files/styles/twoup_layout_desktop_1080/public/2025-08/Lutathera_logo_RGB-810x270-v2.png.webp?itok=WXlSjWSy) 
 
 
 
 
 
 
