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A real-world disproportionality analysis of colchicine: data mining of the public version of FDA Adverse Event Reporting System.
タグ:
FAERS
2024/12/12
Anticoagulant-associated calciphylaxis: analysis of USFDA adverse event report system and clinical feature analysis of reported cases.
タグ:
FAERS
2024/12/11
Interstitial lung disease with antibody-drug conjugates: a real-world pharmacovigilance study based on the FAERS database during the period 2014-2023.
タグ:
FAERS
2024/12/11
Adverse reactions of immune checkpoint inhibitors combined with angiogenesis inhibitors: A pharmacovigilance analysis of drug-drug interactions.
タグ:
FAERS
2024/12/11
Mogamulizumab-Associated Autoimmune Diseases: Insights From FAERS Database Analysis.
タグ:
FAERS
2024/12/11
Mining and analysis of adverse events profile of Guanfacine using FDA Adverse Event Reporting System (FAERS) database.
タグ:
FAERS
2024/12/13
Reproductive Toxicity Induced by Serotonin-Norepinephrine Reuptake Inhibitors: A Pharmacovigilance Analysis From 2004 to 2023 Based on the FAERS Database.
タグ:
FAERS
2024/12/13
A 13-years pharmacovigilance analysis of novel hormonal agents in prostate cancer using the FDA adverse event reporting system database.
タグ:
FAERS
2024/12/13
Vancomycin and linezolid: severe cutaneous adverse reactions to drugs.
タグ:
FAERS
2024/12/12
Neurotoxicity and Rare Adverse Events in BCMA-Directed CAR T Cell Therapy: A Comprehensive Analysis of Real-World FAERS Data.
タグ:
FAERS
2024/12/14
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