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A retrospective study of Food and Drug Administration's (FDA) Adverse Events Reporting System (FAERS) to assess hepatitis B reactivation occurring with PD-1/PD-L1 inhibitors

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A retrospective study of Food and Drug Administration's (FDA) Adverse Events Reporting System (FAERS) to assess hepatitis B reactivation occurring with PD-1/PD-L1 inhibitors

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 08 Feb 2022

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