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Clozapine and hematologic adverse reactions: Impact of the Risk Evaluation and Mitigation Strategy program.
タグ:
FAERS
2020/5/19
Colitis following the use of immune checkpoint inhibitors: A real-world analysis of spontaneous reports submitted to the FDA adverse event reporting system.
タグ:
FAERS
2020/5/19
Hematological toxicities in immune checkpoint inhibitors: A pharmacovigilance study from 2014 to 2019.
タグ:
FAERS
2020/5/10
Combining Social Media and FDA Adverse Event Reporting System to Detect Adverse Drug Reactions.
タグ:
FAERS
2020/5/10
Hematological toxicities in immune checkpoint inhibitors: A pharmacovigilance study from 2014 to 2019.
タグ:
FAERS
2020/5/10
A Modified Skip-Gram Algorithm for Extracting Drug-Drug Interactions from AERS Reports.
タグ:
FAERS
2020/5/1
A Disproportionality Analysis of the Adverse Drug Events Associated with Lurasidone in Paediatric Patients Using the US FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2020/4/6
Cardiovascular Toxicity of Tyrosine Kinase Inhibitors Used in Chronic Myeloid Leukemia: An Analysis of the FDA Adverse Event Reporting System Database (FAERS).
タグ:
FAERS
2020/4/3
Safety signals for QT prolongation or Torsades de Pointes associated with azithromycin with or without chloroquine or hydroxychloroquine.
タグ:
FAERS
2020/4/25
Public Adverse Event Data Insights into the Safety of Pembrolizumab in Melanoma Patients.
タグ:
FAERS
VigiBase
2020/4/25
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