Can AI really outperform traditional methods in AE monitoring from literature?

We recently put this to the test.

In a pilot study, our team compared Insilicomโ€™s IPV platform with traditional Boolean keyword searches for detecting adverse events (AEs).

We focused on three well-known post-market drugs:

๐Ÿ’Š Nivolumab, Dupilumab, and Semaglutide.

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๐Ÿ” What we tested

โ€ข Both methods used the same drug names/synonyms and time window

โ€ข Traditional Boolean approach required โ€œdrug block + AE blockโ€ queries, due to the labor cost to manually read all the articles if AE block is not used.

โ€ข IPV searched only drug names and found nearly 2ร— more relevant publications. This allows more AEs to be detected.

Our AI method was used to extract AEs from all the articles found by both methods. No manual reviews were involved. From a benchmark dataset, we should that our AI method has a 98% recall when detecting articles with AEs.

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๐Ÿ“ˆ The results

30% more AEs detected โ€” IPV uncovered critical literature missed by traditional Boolean searches

Greater efficiency โ€” reduced manual review, faster turnaround, reproducible outcomes

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๐Ÿ› Why it matters

We presented these findings at an FDA meeting, highlighting how AI can strengthen pharmacovigilance workflows and improve drug safety monitoring.

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๐Ÿš€ Want to see it in action?

We invite pharmacovigilance and drug safety teams to try IPV or run a pilot study โ€” and experience how AI can transform your literature surveillance.

#Pharmacovigilance #DrugSafety #ArtificialIntelligence #LiteratureSurveillance #Nivolumab #Dupilumab #Semaglutide

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