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​​​​The content of this website has been produced in line with the SUTENT® (sunitinib malate) Summary of Product Characteristics for Great Britain. 

Click here for the SUTENT® (sunitinib malate) Prescribing Information for Great Britain and Northern Ireland. Adverse event reporting information can be found at the bottom of the page.

SUTENT

SUTENT (sunitinib malate) is indicated for the treatment of advanced and/or metastatic renal cell carcinoma (mRCC) in adults.1​​​​​​​​​​​​​​

 Dosing

Dosing and monitoring requirements for SUTENT

 More Information Loading Efficacy

Patient subgroups and clinical efficacy.

 Learn More Loading Safety Profile

Important safety information and safety outcomes

 See Results LoadingSUTENT (sunitinib malate) mode of action

An introductory video to SUTENT (sunitinib malate) Mode of Action

Support for Your Patients

SUTENT (sunitinib malate) resources to support your patients including a treatment information leaflet and caregivers information brochure

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mRCC : Metastatic Renal Cell Carcinoma​​​​​​​

References

SUTENT® Summary of Product Characteristics for Great Britain click here. SUTENT® Summary of Product Characteristics for Northern Ireland click here.
PP-SUT-GBR-0779 September 2023

Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search 

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Adverse events should also be reported to Pfizer Medical Information on 01304 616161

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