Analysis of nationwide adverse event reports on Isoniazid and Rifampin in tuberculosis prevention and treatment in South Korea. [PDF]
Ryu J, Lee Y, Kwon JW.
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A post-marketing disproportionality analysis of the safety of ribociclib based on the FDA Adverse Event Reporting System. [PDF]
Xu J, Wang R, Shen K.
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Drug-induced herpes zoster: a pharmacovigilance analysis of FDA adverse event reports from 2004 to 2024. [PDF]
Xia J, Zhang J, Zhu H, Ding L.
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Behavioral Economic Strategies Increase Adverse Event Reporting in Pediatric Anesthesia. [PDF]
Guan TK+4 more
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Reply: [Post-marketing safety concerns with Lecanemab: a disproportionality analysis using the FDA adverse event reporting system]. [PDF]
Xing X, Wang K, Dong X.
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Disproportionality analysis of post-marketing safety concerns associated with selumetinib in the FDA adverse event reporting system. [PDF]
Liu F, Su H, Wei W.
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Neurosurgical management of brain metastases in the elderly: a prospective study on adverse event prevalence and predictors. [PDF]
Lenga P+5 more
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Analysis of ADR reports of cetuximab based on the FDA adverse event reporting system database. [PDF]
Zhao S, Wang Y, Deng X, Chen X, Lu Z.
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Safety of creatine supplementation: analysis of the prevalence of reported side effects in clinical trials and adverse event reports. [PDF]
Kreider RB+4 more
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A real-world Pharmacovigilance study of brodalumab based on the FDA adverse event reporting system. [PDF]
He K+9 more
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