FDA MedWatch Report for Nausea Adverse Reaction – Case ID 24287661, unspecified suspect product.

FDA MedWatch Report for Nausea Adverse Reaction – Case ID 24287661, unspecified suspect product.

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Original Request: • Request for MedWatch Report for Product Case ID 24287661 • Suspect Product: NA • Reaction: Nausea • Female of unspecified age • Country of occurrence: US • Manufacturer Control Number: US-SANDOZ INC.-SDZ2024US077299
  • 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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