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A Pharmacovigilance Analysis of Post-Marketing Safety of Tezepelumab.
タグ:
FAERS
2024/11/13
Drug risks associated with sarcopenia: a real-world and GWAS study.
タグ:
FAERS
2024/11/13
Adverse event profile of albumin-bound paclitaxel: a real-world pharmacovigilance analysis.
タグ:
FAERS
2024/11/13
Adverse events associated with oseltamivir and baloxavir marboxil in against influenza virus therapy: A pharmacovigilance study using the FAERS database.
タグ:
FAERS
2024/11/14
Safety assessment of sapropterin dihydrochloride: real-world adverse event analysis based on the FDA adverse event reporting system (FAERS).
タグ:
FAERS
2024/11/14
Quantitative Structure-Activity Relationship Models to Predict Cardiac Adverse Effects.
タグ:
FAERS
2024/11/13
Disseminated intravascular coagulation is an underestimated but fatal adverse event associated with blinatumomab therapy: A pharmacovigilance analysis of FAERS.
タグ:
FAERS
2024/11/13
Investigating the Safety Profile of Fast-Track COVID-19 Drugs Using the FDA Adverse Event Reporting System Database: A Comparative Observational Study.
タグ:
KAERS
FAERS
2024/11/13
Mapping global public perspectives on mRNA vaccines and therapeutics.
タグ:
VAERS
FAERS
2024/11/15
Progressive multifocal leukoencephalopathy associated with sphingosine-1-phosphate receptor modulators: A large case series.
タグ:
FAERS
2024/11/15
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