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Home › Research › Topics › adverse-events

adverse-events

4 studies tagged adverse-events, dated 2024-01-01 to 2026-09-24. Bibliography: BibTeX (.bib) · RIS (.ris)

Newest in this topic

  1. Disproportionality analysis of adverse event signals associated with seven Alzheimer's drugs: insights from the FAERS database 2026-09-24
  2. Comparison of safety of lecanemab and donanemab: a real-world disproportionality analysis using the FDA adverse event reporting system 2026-06-22
  3. A real-world safety surveillance study of aducanumab through the FDA adverse event reporting system 2025-03-13

Studies

4 studies carry this tag.

Date range

2024 to 2026

Top journals

  • Frontiers in pharmacology 3
  • Journal of Alzheimer's disease : JAD 1

Newest first, then by address. Each study has a usefulness score out of 100 (rubric version 4.0); tap a score to see what makes it up. Tags were assigned automatically from each study's title and summary. The same studies as a filter in the library.

  1. Disproportionality analysis of adverse event signals associated with seven Alzheimer's drugs: insights from the FAERS database

    ✓ Peer-reviewed alzhub usefulness score 59 out of 100. Frontiers in pharmacology 2026-09-24 Treatments

    This study utilized FAERS data to compare adverse event reporting signals for seven anti-AD drugs.

  2. Comparison of safety of lecanemab and donanemab: a real-world disproportionality analysis using the FDA adverse event reporting system

    ✓ Peer-reviewed alzhub usefulness score 57 out of 100. Frontiers in pharmacology 2026-06-22 Treatments

    Although both agents have demonstrated therapeutic potential, their post-marketing adverse event reporting profiles remain insufficiently characterized and compared in spontaneous reporting systems.

  3. A real-world safety surveillance study of aducanumab through the FDA adverse event reporting system

    ✓ Peer-reviewed alzhub usefulness score 57 out of 100. Frontiers in pharmacology 2025-03-13 Treatments

    Our real-world analysis identified ARIA-related events as the primary safety concern for aducanumab, typically occurring within 146 days of treatment initiation, with comparable safety profiles across sex but heightened risks in patients ≥75 years.

  4. Adverse Events as a Cause of Unblinding of Allocated Arms in Anti-Amyloid Therapy Trials: A Meta-Analysis of the Predictive Value

    ✓ Peer-reviewed alzhub usefulness score 69 out of 100. Journal of Alzheimer's disease : JAD 2024-01-01 Treatments

    Anti-amyloid drugs for early Alzheimer's disease, including lecanemab, are associated with adverse events (AEs), such as amyloid-related imaging abnormalities (ARIA)-edema/effusion (E), ARIA-hemorrhage, and infusion-related reactions, which can indicate allocated arms in clinical trials.

All topic tags with their study counts