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Novel anti-psoriasis agent-associated cardiotoxicity, analysis of the FDA adverse event reporting system (FAERS).
タグ:
FAERS
2024/2/2
Biologics for asthma and risk of pneumonia.
タグ:
FAERS
2024/1/31
Drug-induced interstitial lung disease: a real-world pharmacovigilance study of the FDA Adverse Event Reporting System from 2004 to 2021.
タグ:
CVAR
FAERS
2024/1/31
Determinants of COVID-19 vaccine-induced myocarditis.
タグ:
FAERS
VAERS
2024/1/31
Association of thrombopoietin-related drugs with thromboembolic events: Mendelian randomization and a real-world study.
タグ:
FAERS
2024/1/31
Identifying new safety risk of human serum albumin: a retrospective study of real-world data.
タグ:
FAERS
2024/1/31
Multivariate generalized mixed-effects models for screening multiple adverse drug reactions in spontaneous reporting systems.
タグ:
FAERS
2024/1/31
Reporting of tumor lysis syndrome with targeted therapy for hepatic cancer in the FDA adverse events reporting system.
タグ:
FAERS
2024/1/30
Detection of novel drug-adverse drug reaction signals in rheumatoid arthritis and ankylosing spondylitis: analysis of Korean real-world biologics registry data.
タグ:
KAERS
FAERS
2024/2/2
Statin-related neurocognitive disorder: a real-world pharmacovigilance study based on the FDA adverse event reporting system.
タグ:
FAERS
2024/1/26
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