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Early Electroconvulsive Therapy in Patients With Major Depressive Disorder: A Propensity Score-Matched Analysis Using a Nationwide Inpatient Database in Japan.
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DPC
2021/4/13
Use of omeprazole, the proton pump inhibitor, as a potential therapy for the capecitabine-induced hand-foot syndrome.
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FAERS
2021/4/28
Analysis of chemotherapy-induced peripheral neuropathy using the Japanese Adverse Drug Event Report database.
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JADER
2021/6/2
Immunotherapies and COVID-19 mortality: a multidisciplinary open data analysis based on FDA’s Adverse Event Reporting System.
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FAERS
2021/7/22
The Association Between Use of Rivastigmine and Pneumonia: Systematic Analysis of FDA Adverse Event Reporting System.
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FAERS
2021/8/17
Leveraging Case Narratives to Enhance Patient Age Ascertainment from Adverse Event Reports.
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FAERS
2021/9/4
Pentosan associated retinal pigmentary changes: FDA’s perspective on an emerging postmarketing safety finding.
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FAERS
2021/9/11
Cardiovascular complications associated with novel agents in the chronic lymphocytic leukemia armamentarium: A pharmacovigilance analysis.
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FAERS
2021/10/16
Cardiovascular, neurological, and pulmonary events following vaccination with the BNT162b2, ChAdOx1 nCoV-19, and Ad26.COV2.S vaccines: An analysis of European data.
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EudraVigilance
2021/10/29
Association between PD-L1 inhibitor, tumor site and adverse events of potential immune etiology within the US FDA adverse event reporting system.
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FAERS
2021/10/29
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