C53572Level 5

Adverse Event and Product Problem Report

**Semantic type:** Intellectual Product

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C25410Adverse Drug Experience Report

C53573Five-Day Report

C53574Seven-Day Report

C53575Ten-Day Report

C53576Fifteen-Day Report

C53577Thirty-Day Report

C53578Periodic Report

C53579Follow-Up Report

C53580FDA Requested Report

C53581Manufacturer Response to Voluntary Report

C53620Initial Adverse Event and Product Problem Report

C68595Spontaneous Report

C68597Mandatory Report

C68599Report from Study

C68622Report from Literature

C68624Expedited Report

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