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Risk of pneumonitis in cancer patients treated with PARP inhibitors: A meta-analysis of randomized controlled trials and a pharmacovigilance study of the FAERS database.
タグ:
FAERS
2021/5/24
A pharmacovigilance study of association between proton pump inhibitor and dementia event based on FDA adverse event reporting system data.
タグ:
FAERS
2021/5/23
Clinical profile of acute pancreatitis following treatment with protease inhibitors: a real-world analysis of post-marketing surveillance data.
タグ:
FAERS
2021/5/22
Certain Public-Reported Immune-mediated Adverse Events for PD-1 Inhibitors in Melanoma Occur at Higher Rates than in Clinical Trials.
タグ:
FAERS
2021/5/21
An OMOP-CDM based pharmacovigilance data-processing pipeline (PDP) providing active surveillance for ADR signal detection from real-world data sources.
タグ:
FAERS
2021/5/19
Disease-modifying agents for multiple sclerosis and the risk for reporting cancer: A disproportionality analysis using the US Food and Drug Administration Adverse Event Reporting System database.
タグ:
FAERS
2021/5/18
Effects of 5-HT(3) receptor antagonists on cisplatin-induced kidney injury.
タグ:
FAERS
2021/5/14
Cardiovascular Toxicities of Antiangiogenic Tyrosine Kinase Inhibitors: A Retrospective, Pharmacovigilance Study.
タグ:
FAERS
2021/5/11
Cardiovascular Safety Profile of Romosozumab: A Pharmacovigilance Analysis of the US Food and Drug Administration Adverse Event Reporting System (FAERS).
タグ:
FAERS
2021/5/1
Thromboembolic Events with Cyclin-Dependent Kinase 4/6 Inhibitors in the FDA Adverse Event Reporting System.
タグ:
FAERS
2021/5/1
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