Comparison of adverse events of poly adenosine diphosphate ribose polymerase inhibitors in patients with ovarian cancer using the United States Food and Drug Administration Adverse Event Reporting System

This study indicates that the types of adverse events may vary by PARP inhibitor and by country. These results will be beneficial in clinical practice.

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Publication Details

Journal
Expert Opinion on Drug Safety
Published
2024-10-18
DOI
https://doi.org/10.1080/14740338.2024.2418333
Primary Topic
PARP inhibition in cancer therapy
Type
article
Field-Weighted Citation Impact
0.00
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article

Comparison of adverse events of poly adenosine diphosphate ribose polymerase inhibitors in patients with ovarian cancer using the United States Food and Drug Administration Adverse Event Reporting System

Chihiro Shiraishi, Toru Ogura
2 links
Expert Opinion on Drug Safety
PARP inhibition in cancer therapy
article

Comparison of adverse events of poly adenosine diphosphate ribose polymerase inhibitors in patients with ovarian cancer using the United States Food and Drug Administration Adverse Event Reporting System

Chihiro Shiraishi, Toru Ogura
article en

Abstract

This study indicates that the types of adverse events may vary by PARP inhibitor and by country. These results will be beneficial in clinical practice.

Expert Opinion on Drug SafetyVol. 24(12)
Mie University Hospital (JP)
Zero hunger
Openalex Percentile: Top 68%
PARP inhibition in cancer therapy
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Comparison of adverse events of poly adenosine diphosphate ribose polymerase inhibitors in patients with ovarian cancer using the United States Food and Drug Administration Adverse Event Reporting System — Chihiro Shiraishi, Toru Ogura · Expert Opinion on Drug Safety (2024) | TGRS Research Map | TGRS