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Myopathy with DPP-4 inhibitors and statins in the real world: investigating the likelihood of drug-drug interactions through the FDA adverse event reporting system.
タグ:
FAERS
2019/6/17
Interaction between paracetamol and lamotrigine: new insights from the FDA Adverse Event Reporting System (FAERS) database.
タグ:
FAERS
2019/6/16
Taking Stock of Dietary Supplements’ Harmful Effects on Children, Adolescents, and Young Adults.
タグ:
FAERS
2019/6/10
Does Industry-Conducted All-Case Surveillance of Newly Approved Oncology Drugs Contribute to the Revision of Package Inserts in Japan?
タグ:
FAERS
2019/5/8
Fournier Gangrene Associated With Sodium-Glucose Cotransporter-2 Inhibitors: A Review of Spontaneous Postmarketing Cases.
タグ:
FAERS
2019/5/7
Discontinuation of Direct Oral Anticoagulants in Response to Attorney Advertisements: Data From the FDA Adverse Event Reporting System.
タグ:
FAERS
2019/5/6
Disruption of podocyte cytoskeletal biomechanics by dasatinib leads to nephrotoxicity.
タグ:
FAERS
2019/5/6
All-Cause Mortality and Cardiovascular Outcomes With Non-Vitamin K Oral Anticoagulants Versus Warfarin in Patients With Heart Failure in the Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2019/5/31
Retrospective Toxicological Profiling of Radium-223 Dichloride for the Treatment of Bone Metastases in Prostate Cancer Using Adverse Event Data.
タグ:
FAERS
2019/5/19
The Impact of Litigation-Associated Reports on Signal Identification in the US FDA’s Adverse Event Reporting System.
タグ:
FAERS
2019/5/18
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