Search results: Sage Journals

Free accessResearch articleFirst published January, 2014

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 accessResearch articleFirst 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 accessResearch articleFirst 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 accessResearch articleFirst 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 accessResearch articleFirst 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

Restricted accessResearch articleFirst 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 accessResearch articleFirst published February, 2026

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 accessResearch articleFirst 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 accessResearch articleFirst published July, 2026

Bone-related adverse events of hormonal therapy: A pharmacovigilance study based on the Food & Drug Administration Adverse Event Reporting System

Yantian Wang, Anqi Li, Jiafu Wang [...]

Journal of International Medical Research

Open accessBrief reportFirst 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

Free accessResearch articleFirst published January, 2014

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 accessResearch articleFirst 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 accessResearch articleFirst 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 accessResearch articleFirst 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 accessResearch articleFirst 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

Restricted accessResearch articleFirst 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 accessResearch articleFirst published February, 2026

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 accessResearch articleFirst 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 accessResearch articleFirst published July, 2026

Bone-related adverse events of hormonal therapy: A pharmacovigilance study based on the Food & Drug Administration Adverse Event Reporting System

Yantian Wang, Anqi Li, Jiafu Wang [...]

Journal of International Medical Research

Open accessBrief reportFirst 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