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Psychiatric Adverse Reactions to Anaplastic Lymphoma Kinase Inhibitors in Non-Small-Cell Lung Cancer: Analysis of Spontaneous Reports Submitted to the FDA Adverse Event Reporting System.
タグ:
FAERS
2022/1/14
Hepatotoxicity reports in the FDA adverse event reporting system database: A comparison of drugs that cause injury via mitochondrial or other mechanisms.
タグ:
FAERS
2022/1/14
A case study of a patient-centered reverse translational systems-based approach to understand adverse event profiles in drug development.
タグ:
FAERS
2022/1/12
Kidney Injury Following Ibuprofen and Acetaminophen: A Real-World Analysis of Post-Marketing Surveillance Data.
タグ:
FAERS
2022/1/11
Analyzing the U.S. Post-marketing safety surveillance of COVID-19 vaccines.
タグ:
VAERS
FAERS
2022/1/11
The Occurrence of Encephalitis Due to Immune Checkpoint Inhibitors: A Pharmacovigilance Study.
タグ:
JADER
2022/1/11
The Importance of Direct Patient Reporting of Adverse Drug Reactions in the Safety Monitoring Process.
タグ:
EudraVigilance
2022/1/12
Post-Marketing Safety Profile of Vortioxetine Using a Cluster Analysis and a Disproportionality Analysis of Global Adverse Event Reports.
タグ:
VigiBase
2022/1/13
Fatal Adverse Events of Dabigatran Combined With Aspirin in Elderly Patients: An Analysis Using Data From VigiBase.
タグ:
VigiBase
2022/1/11
Development and validation of a procedure-based organ failure assessment model for patients in the intensive care unit: an administrative database study.
タグ:
DPC
2022/1/7
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