ENTITY
FDA Adverse Event Reporting System
FDA Adverse Event Reporting System
PulseAugur coverage of FDA Adverse Event Reporting System — every cluster mentioning FDA Adverse Event Reporting System across labs, papers, and developer communities, ranked by signal.
Total · 30d
2
2 over 90d
Releases · 30d
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0 over 90d
Papers · 30d
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1 over 90d
TIER MIX · 90D
TOPICS
SENTIMENT · 30D
1 day(s) with sentiment data
RECENT · PAGE 1/1 · 2 TOTAL
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New metric boosts LLM causality assessment in drug safety reporting
Researchers have developed a novel method to optimize large language models (LLMs) for assessing causality in pharmacovigilance, aiming to improve the accuracy of identifying adverse drug events. A study utilizing OpenA…
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Open-source tool grants AI full access to pharma R&D data
An open-source project called drug-pipeline-mcp has been released, offering AI agents comprehensive access to pharmaceutical R&D data. This tool aggregates information on clinical trials, FDA/EMA approvals, safety repor…