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T-cell malignancies following CAR T-Cell therapy: insights from the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2024/12/19
Safety of talimogene laherparepvec: a real-world retrospective pharmacovigilance study based on FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2024/12/19
Data mining in FAERS: association of newer-generation H1-antihistamines with nervous system disorders.
タグ:
FAERS
2024/12/19
A real-world disproportionality analysis of the US Food and Drug Administration (FDA) adverse event reporting system (FAERS) events for Durvalumab.
タグ:
FAERS
2024/12/19
Hematopoietic adverse events associated with PARP Inhibitors:A FAERS database study.
タグ:
FAERS
2024/12/20
Analysis of the relationship between antineoplastic drugs and suicide-related adverse events based on the food and drug administration adverse event reporting system database.
タグ:
FAERS
2024/12/19
Prevalence and patterns of testing for anaemia in primary care in England: a cohort study using an electronic health records database.
タグ:
CPRD
2024/12/11
Underlying disease risk among patients with fatigue: a population-based cohort study in primary care.
タグ:
CPRD
2024/12/11
Contribution of infection to mortality in people with type 2 diabetes: a population-based cohort study using electronic records.
タグ:
CPRD
2024/12/13
Treatment patterns and burden of uncomplicated urinary tract infection in England: a retrospective cohort study.
タグ:
CPRD
2024/12/13
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