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Re-assessing the risk-benefit profile of Thiazolidinediones: Cardiovascular Risks and Stroke Prevention Through Real-World Data.
タグ:
FAERS
2025/4/18
Emerging and Established Adverse Events of Pasireotide: A Twelve-Year Pharmacovigilance Study.
タグ:
FAERS
2025/4/18
Long-term surveillance of the anti-amyloid monoclonal antibody lecanemab: rights and duties of pharmacovigilance.
タグ:
FAERS
2025/4/12
Drug-induced kidney stones: a real-world pharmacovigilance study using the FDA adverse event reporting system database.
タグ:
FAERS
2025/4/11
A real-world pharmacovigilance case/non-case study of FDA adverse event reporting system events for mannitol.
タグ:
FAERS
2025/4/11
Dementia-related adverse events associated with direct oral anticoagulants use: a real-world, pharmacovigilance study based on the FAERS database.
タグ:
FAERS
2025/4/10
Pharmacovigilance study of immunomodulatory drug-related adverse events using spontaneous reporting system databases.
タグ:
JADER
FAERS
2025/4/10
Drug-induced herpes zoster: a pharmacovigilance analysis of FDA adverse event reports from 2004 to 2024.
タグ:
FAERS
2025/4/10
Pharmacovigilance study of adverse reactions of anti-HER-2 drugs for the treatment of HER-2-positive breast cancer based on the FAERS database.
タグ:
FAERS
2025/4/10
Real-world safety of deucravacitinib: insights from the Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2025/4/9
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