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A 13-years pharmacovigilance analysis of novel hormonal agents in prostate cancer using the FDA adverse event reporting system database.
タグ:
FAERS
2024/12/13
Vancomycin and linezolid: severe cutaneous adverse reactions to drugs.
タグ:
FAERS
2024/12/12
Neurotoxicity and Rare Adverse Events in BCMA-Directed CAR T Cell Therapy: A Comprehensive Analysis of Real-World FAERS Data.
タグ:
FAERS
2024/12/14
Comment on “Evaluation of anticancer therapy-related dermatologic adverse events: Insights from Food and Drug Administration’s adverse event reporting system dataset”.
タグ:
FAERS
2024/12/12
Thromboembolic events associated with combined oral contraceptives: a real-world study based on the FDA adverse event reporting system (FAERS) database.
タグ:
FAERS
2024/12/6
Association between cyclin-dependent kinase 4/6 inhibitors and nephrotoxicity in patients with breast cancer: A Systematic Review and meta-analysis.
タグ:
FAERS
2024/12/6
Signal detection and analysis of sulfasalazine adverse reaction events based on the US FDA adverse event reporting database.
タグ:
FAERS
2024/12/6
Pulmonary adverse events associated with amiodarone: a real-world pharmacovigilance study based on the FDA adverse event reporting system.
タグ:
FAERS
2024/12/6
Sex-differences in reporting of statin-associated diabetes mellitus to the US Food and Drug Administration.
タグ:
FAERS
2024/12/6
Real-world safety evaluation of atorvastatin: insights from the US FDA adverse event reporting system (FAERS).
タグ:
FAERS
2024/12/5
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