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FDA Adverse Event Reports and SBA – OXBRYTA (Voxelotor)
FDA Adverse Event Reports and SBA – OXBRYTA (Voxelotor)
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Original Request: 1) All Adverse Event Reporting data for OXBRYTA (voxelotor) 2) Summary basis of approval for application for OXBRYTA (voxelotor)
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- 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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