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Comparison of brand versus generic antiepileptic drug adverse event reporting rates in the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS).
タグ:
FAERS
2017/6/24
Leveraging Food and Drug Administration Adverse Event Reports for the Automated Monitoring of Electronic Health Records in a Pediatric Hospital.
タグ:
FAERS
2017/6/22
An Algorithm to Identify Generic Drugs in the FDA Adverse Event Reporting System.
タグ:
FAERS
2017/6/9
The impact of database restriction on pharmacovigilance signal detection of selected cancer therapies.
タグ:
FAERS
2017/6/8
From Harmful Treatment to Secondary Gain: Adverse Event Reporting in Dyspepsia and Gastroparesis.
タグ:
FAERS
2017/06/04
Importance of Reverse Translational Research (rTR).
タグ:
FAERS
2017/6/2
Local anesthetics systemic toxicity association with exparel (bupivacaine liposome)- a pharmacovigilance evaluation.
タグ:
FAERS
2017/05/26
Effect of statins on blood pressure: Analysis on adverse events released by FDA.
タグ:
FAERS
2017/5/18
Statin Induced Rhabdomyolysis with Non Oliguric Renal Failure: A Rare Presentation.
タグ:
FAERS
2017/5/18
Analysis of National Pharmacovigilance Data Associated with Statin Use in Korea.
タグ:
KAERS
2017/5/14
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