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A cautionary note regarding the use of the FDA adverse event reporting system.
タグ:
FAERS
2025/7/1
Drug-Associated Alcohol Intolerance: A Real-World Disproportionality Analysis Study.
タグ:
FAERS
2025/7/1
Association between finasteride with subjective memory deficits: a study from the NHANES and FAERS databases.
タグ:
FAERS
2025/7/1
Postmarketing safety surveillance of 177 Lu-DOTA-TATE (LUTATHERA): an observational, pharmacovigilance study leveraging FAERS database.
タグ:
FAERS
2025/7/1
Abortion adverse events associated with adalimumab, etanercept, ustekinumab, and dupilumab during pregnancy: A pharmacovigilance study based on FDA adverse event reporting system.
タグ:
JADER
FAERS
2025/7/1
Disproportionality Analysis of Ivabradine in the US FDA Adverse Event Reporting System: A Real-World Study Across Overall and Indication-Specific Populations.
タグ:
FAERS
2025/7/1
Disruption of small intestinal mucosal homeostasis in mice with amiodarone induced steatohepatitis.
タグ:
JADER
2025/7/3
Comparative assessment of endoscopic and microsurgery resection for intracranial ventricular tumors: a meta-analysis of 3059 patients.
タグ:
JADER
2025/7/1
Factors associated with the completeness of information provided in adverse drug reaction reports of physicians, pharmacists and consumers from Germany.
タグ:
EudraVigilance
2025/7/4
Pharmacovigilance on Dexamethasone 1 mg/mL + Levofloxacin 5 mg/mL Eye Drops, Solution: A Five-Year Registry.
タグ:
EudraVigilance
2025/7/2
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