Assessment of PET Drug Adverse Events in the U.S. since the Implementation of 21 CFR part 212
Dakanali M; VanBrocklin HF; Zigler SS; Scott PJH · 2026 · Preprint
WASTE classifies this as Negative / Null Result Report · AI classification, approximate
The study found no significant effect — useful as a negative control or null benchmark for your own design.
Abstract (excerpt)
Abstract Background : Multiple new PET radiopharmaceuticals (RPhs) have recently been approved by the U.S. Food and Drug Administration (FDA). Despite the generally accepted safety profile of PET RPhs supported by millions of doses…
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Metadata source: Europe PMC · DOI 10.21203/rs.3.rs-9826575/v1