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Influence of anticancer agents on sexual function: An in vivo study based on the US FDA Adverse Event Reporting System.
タグ:
FAERS
2021/8/15
Stevens-Johnson syndrome/toxic epidermal necrolysis in patients treated with immune checkpoint inhibitors: A safety analysis of clinical trials and FDA pharmacovigilance database.
タグ:
FAERS
2021/8/14
Neoplasm Reports in Food and Drug Administration Adverse Event Reporting System Following Angiotensin Receptor Blocker Recalls.
タグ:
FAERS
2021/8/13
Assessment of adverse events associated with remdesivir use for coronavirus disease 2019 using real-world data.
タグ:
FAERS
2021/7/31
Drug-induced liver injury associated with lopinavir-ritonavir in patients with COVID-19: a disproportionality analysis of U.S. food and drug administration adverse event reporting system (FAERS) data.
タグ:
FAERS
2021/7/31
Analysis of the Frequency and Onset Time of Hyponatremia/Syndrome of Inappropriate Antidiuretic Hormone Induced by Antidepressants or Antipsychotics.
タグ:
FAERS
2021/7/3
Molecular Initiating Events Associated with Drug-Induced Liver Malignant Tumors: An Integrated Study of the FDA Adverse Event Reporting System and Toxicity Predictions.
タグ:
FAERS
2021/7/3
Does HIF-PHI increased risk of gastrointestinal hemorrhage in patients with renal anemia: a review of cases reported to the U.S. Food and drug administration adverse event reporting system.
タグ:
FAERS
2021/7/29
Immune-related adverse event profile of combination treatment of PD-(L)1 checkpoint inhibitors and bevacizumab in non-small cell lung cancer patients: data from the FDA adverse event reporting system.
タグ:
FAERS
2021/7/24
DPP-4 Inhibitors and Increased Reporting Odds of Bullous Pemphigoid: A Pharmacovigilance Study of the FDA Adverse Event Reporting System (FAERS) from 2006 to 2020.
タグ:
FAERS
2021/7/22
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