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Retricted access

Research article

First published 2021-6

Adverse event profile differences between rituximab and ocrelizumab: Findings from the FDA Adverse Event Reporting Database

Natalia Gonzalez Caldito, Afsaneh Shirani, Amber Salter [...]

Multiple Sclerosis Journal

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

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Research article

First published 2000-11

Safety profile and causes of withdrawal due to adverse events in systemic lupus erythematosus patients treated long-term with cyclosporine A

F Conti, R Priori, C Alessandri [...]

Lupus

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Research article

First published 2025-2

Unveiling the safety profile of lecanemab: A comprehensive analysis of adverse events using FDA adverse event reporting system data

Wukun Ge, Yingyan Yan, Yaoyao Hu [...]

Journal of Alzheimer’s Disease

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

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Research article

First published 2018-5

Comparison of Serious Adverse Event Profiles Among Antirheumatic Agents Using Japanese Adverse Drug Event Report Database

Yomei Matsuoka, Mamoru Narukawa

Therapeutic Innovation & Regulatory Science

Open access

Research article

First published 2024

Adverse event profiles of CDK4/6 inhibitors: data mining and disproportionality analysis of the FDA adverse event reporting system

Jun Shen, Pingli Luo, Jianmei Xu

Therapeutic Advances in Drug Safety

Open access

Research article

First published 2018-11

Differential profiles of adverse events associated with mycophenolate mofetil between adult and pediatric renal transplant patients

Keiko Hosohata, Etsuko Matsuoka, Ayaka Inada [...]

Journal of International Medical Research

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

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Research article

First published 2025-08

Real-World Safety Profile of Cenegermin Per FDA Adverse Event Reporting System

Hassaam S. Choudhry, Mingzhuo Pei, David Mothy [...]

Journal of Ocular Pharmacology and Therapeutics

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