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Drug-induced hypokalemia: an analytical study based on real-world drug monitoring data.
タグ:
FAERS
2025/2/20
Adverse event profiles of CDK4/6 inhibitors: a disproportionality analysis of the FDA Adverse Event Reporting System (FAERS) database.
タグ:
FAERS
2025/2/20
A real-world pharmacovigilance analysis of hepatitis B vaccine using the U.S. Vaccine Adverse Event Reporting System (VAERS) database.
タグ:
VAERS
FAERS
2025/2/20
What does real-world data reveal about cangrelor’s safety? An analysis of FDA adverse event reporting system (FAERS) database.
タグ:
FAERS
2025/2/20
Assessment of adverse events of the novel antiepileptic drug lamotrigine: a real-world pharmacovigilance study based on FAERS.
タグ:
FAERS
2025/2/18
Drug-induced skin ulcer: real-world pharmacovigilance analysis based on the FDA adverse event reporting system.
タグ:
FAERS
2025/2/18
Potential risk analysis of antipsychotics-related constipation from the FDA Adverse Event Reporting System.
タグ:
FAERS
2025/2/18
Novel insights into post-marketing AEs associated with bempedoic acid: a comprehensive analysis utilizing the FAERS database.
タグ:
FAERS
2025/2/17
Hepatic adverse events with CDK4/6 inhibitors: a systematic review combining meta-analysis and FAERS database.
タグ:
FAERS
2025/2/17
Toxicity spectrum of taxanes: A safety analysis from pre-marketing to post-marketing.
タグ:
FAERS
2025/2/17
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