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Pharmacovigilance analysis and real-world adverse event profile (safety signals and product-related issues) of potassium citrate: a US FDA adverse event reporting system (FAERS) based analysis.
タグ:
FAERS
2026/4/28
Interstitial lung disease associated with novel anticancer agents in non-small cell lung cancer: a pharmacovigilance analysis using the FAERS database.
タグ:
FAERS
2026/4/28
Pharmacovigilance study of spinal epidural hematoma reports associated with direct oral anticoagulants and warfarin.
タグ:
FAERS
2026/5/1
Association between immune-mediated cystitis and PD-1, PD-L1, CTLA-4, and LAG-3 immune checkpoint inhibitors: A pharmacovigilance study from the FAERS database.
タグ:
FAERS
2026/4/30
Spectrum and prognosis of CAR-T-related endocrine toxicity: glucose/calcium dysregulation, pituitary axis disorders, and overlap with CRS.
タグ:
FAERS
2026/4/30
Post-marketing safety evaluation of paroxetine: a real-world pharmacovigilance analysis based on the FDA adverse event reporting system.
タグ:
KAERS
FAERS
2026/4/30
Exploring Risk Drugs and Mechanisms in Dystonia: Insights from Pharmacovigilance and Proteogenomics.
タグ:
FAERS
2026/4/29
Pemphigoid associated with quinolone antibiotics: a real-world pharmacovigilance study of the FDA adverse event reporting system and literature-based evidence.
タグ:
FAERS
2026/5/1
Adverse events profiles of pemetrexed: a Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2026/5/1
The Real-World Endocrine Toxicity Profile of ICIs, VEGFR-TKIs, and Their Combination: Analysis of the FDA Adverse Event Reporting System (FAERS) Database.
タグ:
FAERS
2026/5/1
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