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Free access

Research article

First published 2014-1

Triptans and serious adverse vascular events: Data mining of the FDA Adverse Event Reporting System database

Giuseppe Roberto, Carlo Piccinni, Roberto D’Alessandro [...]

Cephalalgia

Open access

Research article

First published 2019

Adverse event profiles of solvent-based and nanoparticle albumin-bound paclitaxel formulations using the Food and Drug Administration Adverse Event Reporting System

Misa Naganuma, Kohei Tahara, Shiori Hasegawa [...]

Sage Open Medicine

Open access

Research article

First published 2020

Assessment of Reye’s syndrome profile with data from the US Food and Drug Administration Adverse Event Reporting System and the Japanese Adverse Drug Event Report databases using the disproportionality analysis

Kiyoka Matsumoto, Shiori Hasegawa, Satoshi Nakao [...]

Sage Open Medicine

Open access

Research article

First published 2025

Pharmacovigilance study of immunomodulatory drug-related adverse events using spontaneous reporting system databases

Satoshi Nakao, Mika Maezawa, Moe Yamashita [...]

International Journal of Immunopathology and Pharmacology

Open access

Research article

First published 2024

Vonoprazan-associated Clostridioides difficile infection: an analysis of the Japanese Adverse Drug Event Report and the FDA Adverse Event Reporting System

Mengling Ouyang, Shupeng Zou, Qian Cheng [...]

Therapeutic Advances in Drug Safety

Retricted access

Research article

First published 2026

Mining of Respiratory System Toxicity Risk Signals for Fulvestrant Based on the Tianjin Adverse Reaction Monitoring Center and the FDA Adverse Event Reporting System Database

Meisa Wang, Qiushuang Han, Yuan Jiang [...]

Hospital Pharmacy

Open access

Research article

First published 2026-2

Safety profile of progesterone: Insights from an FDA Adverse Event Reporting System (FAERS)–based pharmacovigilance study

Ren Xu, Xiaona Wang, Junqin Zhang [...]

Journal of International Medical Research

Open access

Research article

First published 2020

Identifying Herbal Adverse Events From Spontaneous Reporting Systems Using Taxonomic Name Resolution Approach

Vivekanand Sharma, Luiz Fernando Fracassi Gelin, Indra Neil Sarkar

Bioinformatics and Biology Insights

Open access

Brief report

First published 2025

Reporting patterns of multiple sclerosis with immune checkpoint inhibitors: analysis of the FDA Adverse Event Reporting System

Afsaneh Shirani, Samuel A. Goldlust, Olaf Stuve

Therapeutic Advances in Neurological Disorders

Retricted access

Research article

First published 2017-3

Cardiotoxicity in targeted therapy for breast cancer: A study of the FDA adverse event reporting system (FAERS)

Saranrat Wittayanukorn, Jingjing Qian, Brandon S Johnson [...]

Journal of Oncology Pharmacy Practice

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