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Male sexual dysfunction associated with GLP-1 receptor agonists: a cross-sectional analysis of FAERS data.
タグ:
FAERS
2025/4/17
A real-world pharmacovigilance analysis of omadacycline in FDA adverse event reporting system (FAERS) database.
タグ:
FAERS
2025/4/16
Epidemiologic investigation on neurological complications following neuraxial anesthesia in 2.7 million cases in Southwest China.
タグ:
FAERS
2025/4/19
Real-World pharmacovigilance analysis of drug-related conjunctivitis using the FDA adverse event reporting system database.
タグ:
FAERS
2025/4/19
Reassessing 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
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