Mengling Ouyang
Wuhan, China
Last Updated: 09/26/2026
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Found 12 publications
Infection toxicity assessment of tumor necrosis factor α inhibitors in the treatment of IBD: a real-world study based on the US food and drug administration adverse events reporting system (FAERS).
Journal: Expert opinion on drug safety
Published: March 29, 2025
Cyclin-dependent kinase 4/6 inhibitor-associated pulmonary toxicity: a disproportionality analysis from 2015 to 2023 based on the FAERS database.
Journal: Expert opinion on drug safety
Published: February 02, 2025
Pulmonary toxicity assessment of tumor necrosis factor α inhibitors in the treatment of IBD: a real world study based on US food and drug administration adverse events reporting system (FAERS).
Journal: Expert opinion on drug safety
Published: December 18, 2024
Post-Marketing Pharmacovigilance of Canakinumab from the FDA Adverse Event Reporting System (FAERS).
Post-Marketing Pharmacovigilance of Canakinumab from the FDA Adverse Event Reporting System (FAERS).
Journal: Pharmaceuticals (Basel, Switzerland)
Published: December 13, 2024
Comparative Efficacy and Safety of Potassium-Competitive Acid Blockers vs. Proton Pump Inhibitors for Peptic Ulcer with or without Helicobacter pylori Infection: A Systematic Review and Network Meta-Analysis.
Journal: Pharmaceuticals (Basel, Switzerland)
Published: May 02, 2024
Coagulation dysfunction events associated with echinocandins: a real-world study from FDA adverse event reporting system (FAERS) database.
Journal: Thrombosis journal
Published: April 13, 2024
A disproportionality analysis of adverse events caused by GnRHas from the FAERS and JADER databases.
A disproportionality analysis of adverse events caused by GnRHas from the FAERS and JADER databases.
Journal: Frontiers in pharmacology
Published: February 28, 2024
Vonoprazan-associated Clostridioides difficile infection: an analysis of the Japanese Adverse Drug Event Report and the FDA Adverse Event Reporting System.
Journal: Therapeutic advances in drug safety
Published: January 16, 2024
Post-marketing safety of anti-IL-5 monoclonal antibodies (mAbs): an analysis of the FDA Adverse Event Reporting System (FAERS).
Journal: Expert opinion on drug safety
Published: August 23, 2023
Showing 1-12 of 12
Last Updated: 09/26/2026