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Facial paralysis and vaccinations: a vaccine adverse event reporting system review.
タグ:
FAERS
VAERS
2021/6/30
Assessing taxane-associated adverse events using the FDA adverse event reporting system database.
タグ:
FAERS
2021/6/3
Real-world experience of ocrelizumab initiation in a diverse multiple sclerosis population.
タグ:
FAERS
2021/6/3
Evaluation of Potential Complications of Interstitial Lung Disease Associated With Antiandrogens Using Data From Databases Reporting Spontaneous Adverse Effects.
タグ:
FAERS
JADER
2021/6/29
Research on Beers Criteria and STOPP/START Criteria based on the FDA FAERS database.
タグ:
FAERS
2021/6/26
Thyroid dysfunction related to vascular endothelial growth factor receptor tyrosine kinase inhibitors: A real-world study based on FAERS.
タグ:
FAERS
2021/6/26
Thromboembolic events associated with immune checkpoint inhibitors: A real-world study of data from the food and drug administration adverse event reporting system (FAERS) database.
タグ:
FAERS
2021/6/16
Feature engineering and machine learning for causality assessment in pharmacovigilance: Lessons learned from application to the FDA Adverse Event Reporting System.
タグ:
FAERS
2021/6/16
Systematic analysis of safety profile for darunavir and its boosted agents using data mining in the FDA Adverse Event Reporting System database.
タグ:
FAERS
2021/6/16
Five Years of Sacubitril/Valsartan-a Safety Analysis of Randomized Clinical Trials and Real-World Pharmacovigilance.
タグ:
FAERS
EudraVigilance
VigiBase
2021/6/15
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