FDA Documents – Turmeric/Liver Injury Adverse Events (Aug–Oct 2024)

FDA Documents – Turmeric/Liver Injury Adverse Events (Aug–Oct 2024)

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Original Request: I request copies of all documents in the possession of FDA, from August 1, 2024, to October 31, 2024, regarding products containing “Turmeric”; “Curcumin”; “Curcuminoids” and “liver toxicity”; “liver damage”; “liver injury”; “hospitalization”. Including any: a) Form FDA 3500 Voluntary Reporting b) Form FDA 3500B Voluntary Reporting for Consumer and c) Form 3500A Mandatory Reporting.
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.

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