A real-world disproportionality analysis of FDA adverse event reporting system events for ibuprofen.
Yi-Kuan DuZhuoming GuoBijun XuYujia YangMianda HuYanghui HuYurong YangMengting ZhangZhenjie WangXiaochun GuoYixing HuangJinfeng ZhuWeichui ZhangChun YangPublished in: Expert opinion on drug safety (2024)
The study explores the important and valuable potential AEs and ADRs of ibuprofen at the SOC and PT levels, respectively. To provide a reference for decision-making for ibuprofen to promote rational clinical dosing.