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Renal adverse effects following the use of different immune checkpoint inhibitor regimens: A real-world pharmacoepidemiology study of post-marketing surveillance data.
タグ:
FAERS
2020/7/29
Safety of fluoxetine use in children and adolescents: a disproportionality analysis of the Food and Drug Administration Adverse Event Reporting System (FAERS) database.
タグ:
FAERS
2020/7/29
Fournier Gangrene Associated with Sodium-Glucose Cotransporter-2 Inhibitors: A Pharmacovigilance Study with Data from the U.S. FDA Adverse Event Reporting System.
タグ:
FAERS
2020/7/23
A real-world disproportionality analysis of FDA Adverse Event Reporting System (FAERS) events for baricitinib.
タグ:
FAERS
2020/7/23
Ovary and uterus related adverse events associated with statin use: an analysis of the FDA Adverse Event Reporting System.
タグ:
FAERS
2020/7/21
Differences in safety profiles of newly approved medications for multiple myeloma in real-world settings versus randomized controlled trials.
タグ:
FAERS
2020/7/21
Mining reported adverse events induced by potential opioid-drug interactions.
タグ:
FAERS
2020/7/2
Patient safety culture and obstacles to adverse event reporting in nursing homes.
タグ:
FAERS
2020/7/16
Tumefactive multiple sclerosis in association with fingolimod initiation and discontinuation.
タグ:
FAERS
2020/7/15
Vemurafenib Induced Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS): A Disproportionality Analysis in FAERS Database.
タグ:
FAERS
2020/7/1
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