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Pulmonary haemorrhage and haemoptysis associated with bevacizumab-related treatment regimens: a retrospective, pharmacovigilance study using the FAERS database.
タグ:
FAERS
2024/7/9
A pharmacovigilance study of chronic kidney disease in diabetes mellitus patients with statin treatment by using the US Food and Drug Administration adverse event reporting system.
タグ:
FAERS
2024/7/8
A real-world pharmacovigilance study of FDA adverse event reporting system events for atogepant.
タグ:
FAERS
2024/7/6
PARP inhibitor-related acute renal failure: a real-world study based on the FDA adverse event reporting system database.
タグ:
FAERS
2024/7/5
Compartment syndrome associations with drugs: a pharmacovigilance study of the FDA adverse event reporting system (FAERS).
タグ:
FAERS
2024/7/5
PARP inhibitor-related acute renal failure: a real-world study based on the FDA adverse event reporting system database.
タグ:
FAERS
2024/7/5
Compartment syndrome associations with drugs: a pharmacovigilance study of the FDA adverse event reporting system (FAERS).
タグ:
FAERS
2024/7/5
Exploring the Relationship Between Atorvastatin and Memory Loss: A Comprehensive Analysis Integrating Real-World Pharmacovigilance and Mendelian Randomization.
タグ:
FAERS
2024/7/4
Analysis of hemorrhagic drug-drug interactions between P-gp inhibitors and direct oral anticoagulants from the FDA adverse event reporting system.
タグ:
FAERS
2024/7/4
Exploring the Relationship Between Atorvastatin and Memory Loss: A Comprehensive Analysis Integrating Real-World Pharmacovigilance and Mendelian Randomization.
タグ:
FAERS
2024/7/4
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