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Safety Profile of Molnupiravir in the Treatment of COVID-19: A Descriptive Study Based on FAERS Data.
タグ:
FAERS
2023/1/9
Risk of Lichen Sclerosus and Lichen Planus in Patients Receiving Immune Checkpoint Inhibitors.
タグ:
FAERS
2023/1/9
Post-Marketing Safety of Vemurafenib: A Real-World Pharmacovigilance Study of the FDA Adverse Event Reporting System.
タグ:
FAERS
2023/1/8
Interstitial pneumonitis associated with combined regimen of immunotherapy and conventional therapies-pharmacovigilance database analysis with real-world data validation.
タグ:
FAERS
2023/1/5
Pharmacovigilance of triazole antifungal agents: Analysis of the FDA adverse event reporting system (FAERS) database.
タグ:
FAERS
2023/1/3
A post-marketing pharmacovigilance study of avapritinib: adverse event data mining and analysis based on the United States Food and Drug Administration Adverse Event Reporting System database.
タグ:
FAERS
2023/1/27
Hyperuricaemia, gout and related adverse events associated with antihypertensive drugs: A real-world analysis using the FDA adverse event reporting system.
タグ:
FAERS
2023/1/27
Analysis of Clinical Factors in Olaparib-related Anemia Using Adverse Drug Event Reporting Databases.
タグ:
FAERS
JADER
2023/1/26
Analysis of drug-induced liver-related adverse event trend reporting between 1997 and 2019.
タグ:
FAERS
JADER
2023/1/22
Evidence of Accidental Dosing Errors with Immediate-Release Sodium Oxybate: Data from the US Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2023/1/21
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