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Assessment of the real-world safety profile of vedolizumab using the United States Food and Drug Administration adverse event reporting system.
タグ:
FAERS
2019/12/5
Tumor lysis syndrome associated with bortezomib: A post-hoc analysis after signal detection using the US Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2019/12/4
Drug Interaction Between Febuxostat and Thiopurine Antimetabolites: A Review of the FDA Adverse Event Reporting System and Medical Literature.
タグ:
FAERS
2019/12/31
Propensity score-adjusted three-component mixture model for drug-drug interaction data mining in FDA Adverse Event Reporting System.
タグ:
FAERS
2019/12/28
Hypoglycemia Associated with Antibiotics Alone and in Combination with Sulfonylureas and Meglitinides: An Epidemiologic Surveillance Study of the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2019/12/22
Association between malignancy and methotrexate and biological disease-modifying antirheumatic drugs in patients with rheumatoid arthritis.
タグ:
FAERS
2019/12/20
Towards early detection of adverse drug reactions: combining pre-clinical drug structures and post-market safety reports.
タグ:
FAERS
2019/12/19
Disproportionality Analysis of Safety with Nafcillin and Oxacillin with the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2019/12/18
Adverse Events Due to Insomnia Drugs Reported in a Regulatory Database and Online Patient Reviews: Comparative Study.
タグ:
FAERS
2019/11/9
Opioids and frequency counts in the US Food and Drug Administration Adverse Event Reporting System (FAERS) database: a quantitative view of the epidemic.
タグ:
FAERS
2019/11/7
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