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Assessing real-world safety of plecanatide: a pharmacovigilance study based on the FDA adverse event reporting system.
タグ:
FAERS
2024/12/10
Post-marketing safety of panitumumab: a real-world pharmacovigilance study.
タグ:
FAERS
2024/12/9
Post-licensure Safety Surveillance of 20-Valent Pneumococcal Conjugate Vaccine (PCV20) Among US Adults in the Vaccine Adverse Event Reporting System (VAERS).
タグ:
VAERS
FAERS
2024/12/12
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
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