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Newly identified adverse events for gemcitabine using the Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2023/11/17
Withdrawn 2.0-update on withdrawn drugs with pharmacovigilance data.
タグ:
FAERS
2023/11/17
Characterizing Adverse Events of Biologic Treatment of T2 Disease: A Disproportionality Analysis of the FDA Adverse Event Reporting System.
タグ:
FAERS
2023/11/15
A pharmacovigilance study of association between proton-pump inhibitors and rhabdomyolysis event based on FAERS database.
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FAERS
2023/11/14
Impact of Covid-19 Vaccination on Spontaneous Pharmacovigilance Reporting in France.
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FPVD
2023/11/6
Antithyroid drug-induced leukopenia and G-CSF administration: a long-term cohort study.
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DeSC
2023/11/8
Predicting hepatic encephalopathy in patients with cirrhosis: A UK population-based study and validation of risk scores.
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CPRD
2023/11/6
Alternative cascade-testing protocols for identifying and managing patients with familial hypercholesterolaemia: systematic reviews, qualitative study and cost-effectiveness analysis.
タグ:
CPRD
2023/11/4
Trends in prevalence, treatment use, and disease burden in patients with eosinophilic granulomatosis with polyangiitis in Japan: Real-world database analysis.
タグ:
MDV
2023/11/6
Patterns of use of symptomatic treatments for Alzheimer’s disease dementia (AD).
タグ:
CPRD
2023/11/10
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