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Drug-induced kidney stones: a real-world pharmacovigilance study using the FDA adverse event reporting system database
Published 2025-03-01Subjects: Get full text
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A disproportionality analysis of FDA adverse event reporting system events for misoprostol
Published 2025-01-01Subjects: Get full text
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Comprehensive analysis of adverse events associated with vortioxetine using the FDA adverse event reporting system
Published 2025-05-01Subjects: Get full text
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Hypoglycemia associated with fluoroquinolone: a pharmacovigilance analysis from 2014 to 2023 based on the FDA adverse event reporting system
Published 2025-05-01Subjects: Get full text
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A pharmacovigilance study of vortioxetine based on data from the FDA adverse event reporting system
Published 2025-08-01Subjects: Get full text
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Disproportionality analysis of oesophageal toxicity associated with oral bisphosphonates using the FAERS database (2004–2023)
Published 2024-11-01Subjects: Get full text
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Signal mining and analysis of ripretinib adverse events: a real-world pharmacovigilance analysis based on the FAERS database
Published 2025-02-01Subjects: Get full text
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A real-world Pharmacovigilance study of brodalumab based on the FDA adverse event reporting system
Published 2025-01-01Subjects: Get full text
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Assessing real-world safety of plecanatide: a pharmacovigilance study based on the FDA adverse event reporting system
Published 2024-11-01Subjects: Get full text
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Conducting a real-world study of Tumor Necrosis factor-alpha inhibitors-induced Systemic Lupus Erythematosus based on the FAERS database
Published 2025-02-01Subjects: Get full text
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Neurological adverse events associated with antidepressants: a comprehensive 22-year analysis of the FDA adverse event reporting system
Published 2025-08-01Subjects: Get full text
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Safety assessment of ripretinib: a real-world adverse event analysis from the food and drug administration adverse event reporting system
Published 2025-03-01Subjects: Get full text
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Drug-induced pulmonary edema: a real-world pharmacovigilance study using the FDA Adverse Event Reporting System (FAERS)
Published 2025-08-01Subjects: Get full text
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Neurological adverse events associated with baclofen: a pharmacovigilance study based on FDA adverse event reporting system
Published 2025-05-01Subjects: Get full text
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Assessment of drug-related migraine in a real-world large-scale database
Published 2025-07-01Subjects: Get full text
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