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Real-world drug safety study of somatostatin analogs based on the food and drug administration adverse event reporting system database.
タグ:
FAERS
2025/8/22
A real-world pharmacovigilance analysis of the FDA adverse event reporting system database for emicizumab.
タグ:
FAERS
2025/8/22
Mining and evaluation of security alert signals of neuroprotective agents based on the Jinan adverse event reporting system database: a retrospective study.
タグ:
FAERS
2025/8/21
Post-marketing safety profile of Ertugliflozin: Insights from a real-world pharmacovigilance analysis based on the FAERS database.
タグ:
FAERS
2025/8/21
Real-world safety of herpes zoster vaccines: A pharmacovigilance study based on the vaccine adverse event reporting system (may 2006-december 2024).
タグ:
VAERS
FAERS
2025/8/21
Updating understanding of real-world adverse events associated with omeprazole.
タグ:
FAERS
2025/8/20
Evaluating the association between migraine treatments and tinnitus: Insights from the US Food and Drug Administration adverse event reporting system.
タグ:
KAERS
FAERS
2025/8/20
A Real-World Disproportionality Analysis of FDA Adverse Event Reporting System Events for Tazemetostat.
タグ:
FAERS
2025/8/20
Pharmacovigilance analysis of metabolic and nutritional adverse reactions associated with entecavir and tenofovir using the FDA adverse event reporting system database.
タグ:
FAERS
2025/8/19
Signal mining and risk analysis of tisotumab vedotin adverse events based on the FAERS database.
タグ:
FAERS
2025/8/19
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