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Hypocalcemia Event Associated with Denosumab: A Real-World Study from FDA Adverse Event Reporting System (FAERS) Database.
タグ:
FAERS
2024/10/25
Adverse events associated with carbamazepine: a pharmacovigilance study using the FDA Adverse Event Reporting System.
タグ:
FAERS
2024/10/25
Adverse events associated with parenteral nutrition support therapy: A pharmacovigilance study.
タグ:
FAERS
2024/10/25
Real-world analysis of levetiracetam-associated rhabdomyolysis: insights from the FDA adverse event reporting system.
タグ:
FAERS
2024/10/23
A real-world pharmacovigilance study of FDA Adverse Event Reporting System (FAERS) for gemcitabine.
タグ:
FAERS
2024/10/23
Association between statin use and immune-related adverse events in patients treated with immune checkpoint inhibitors: analysis of the FAERS database.
タグ:
FAERS
2024/10/23
The Association Between Dextromethorphan/Bupropion with Alcohol and Substance Misuse: Reports to the Food and Drug Administration Adverse Event Reporting System (FAERS).
タグ:
CVAR
FAERS
2024/10/23
Adverse events analysis of Relugolix (Orgovyx(R)) for prostate cancer based on the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2024/10/22
Cardiovascular adverse events associated with triptans for treatment of migraine: a pharmacovigilance study of the FDA adverse event reporting system (FAERS).
タグ:
FAERS
2024/10/22
Mining and analysis of adverse event signals for alendronate based on the real-world data of FDA adverse event reporting system database.
タグ:
FAERS
2024/10/22
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