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FDA FAERS Case Reports – Lutathera (Lutetium Lu 177 Dotatate) Adverse Effects/Toxicities (Groups of 12 Cases, 2024)
FDA FAERS Case Reports – Lutathera (Lutetium Lu 177 Dotatate) Adverse Effects/Toxicities (Groups of 12 Cases, 2024)
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Original Request Contents: Request case reports on adverse effects/toxicities associated with Lutathera (lutetium Lu 177 dotatate) in groups of 12 cases (academic purpose). (2024)
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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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