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Reporting Frequency of Antipsychotics-Induced Tardive Dyskinesia and Other Extrapyramidal Symptoms: Analysis Based on a Spontaneous Reporting System Database in Japan.
タグ:
JADER
2025/9/12
A real-world pharmacovigilance study of FDA Adverse Event Reporting System events for gefitinib and docetaxel.
タグ:
FAERS
2025/9/6
Olmesartan-Induced Enteropathy: Case Reports and Insights From FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2025/9/6
Overall safety evaluation of the risk signals of sacubitril/valsartan: A postmarketing pharmacoepidemiology study from 2015 to 2024.
タグ:
FAERS
2025/9/10
Drug-associated postpartum hemorrhage: a comprehensive disproportionality analysis based on the FAERS database.
タグ:
FAERS
2025/9/9
Real-world pharmacovigilance assessment of drug-induced male hypogonadism risks: An analysis of FDA adverse drug event data.
タグ:
FAERS
2025/9/9
Drug-induced vitiligo: a real-world pharmacovigilance analysis of the FAERS database.
タグ:
FAERS
2025/9/8
Post-marketing safety surveillance of pneumococcal vaccines: a real-world pharmacovigilance study using the U.S. vaccine adverse event reporting system (VAERS) database.
タグ:
VAERS
FAERS
2025/9/11
An application of studying FAERS data to Enhance Drug Safety and Treatment Outcomes in Rare Diseases.
タグ:
FAERS
2025/9/11
Antiplatelet therapy and central nervous system hematomas: a cohort study using real-world data from the FAERS and vigiaccess databases.
タグ:
FAERS
2025/9/10
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