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Drug combination choices of 5alpha-reductase inhibitors and alpha-blockers in patients with benign prostatic hyperplasia: a study based on the FAERS database.
タグ:
FAERS
2026/6/30
Adverse events and vaccine administration errors following RSV vaccination: Findings from the United States VAERS database, 2023-2025.
タグ:
VAERS
FAERS
2026/6/30
Detection of drug-induced acute respiratory distress syndrome risk signals in FAERS: a real-world pharmacovigilance study.
タグ:
FAERS
2026/6/29
Adverse Event Profiling and Comparative Analysis of HER2-targeting Antibody-drug Conjugates Using Pharmacovigilance Databases.
タグ:
JADER
FAERS
2026/7/1
Safety evaluation of CD3xCD20 bispecific antibodies: a pharmacovigilance study using FDA adverse event reporting system.
タグ:
FAERS
2026/7/1
Safety profile of upadacitinib in inflammatory Bowel disease: a dual-source pharmacovigilance study integrating FAERS signal detection and real-world clinical cohort analysis.
タグ:
FAERS
2026/6/30
Signal mining of adverse reactions for neuraminidase inhibitors in pregnant women: a disproportionality analysis based on the FDA adverse event reporting system database.
タグ:
FAERS
2026/7/1
Immune effector cell-associated hematotoxicity following CAR-T cell therapies: insights from a large national database.
タグ:
FAERS
2026/7/1
Evaluating Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis Associated With Newer Antiseizure Medications Using FAERS and JADER Combined With Bioinformatics Exploration.
タグ:
JADER
FAERS
2026/7/1
Severe renal and pancreatic toxicities associated with ipilimumab and nivolumab combination therapy in non-small cell lung cancer: a pharmacovigilance analysis of the FDA adverse event reporting system.
タグ:
FAERS
2026/7/2
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