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The impact of immunotherapies on COVID-19 case fatality rates during the US vaccination campaign: a multidisciplinary open data analysis using FDA Adverse Event Reporting System and Our World in Data.
タグ:
FAERS
2023/7/3
Six Years of the US Food and Drug Administration’s Postmarket Active Risk Identification and Analysis System in the Sentinel Initiative: Implications for Real World Evidence Generation.
タグ:
FAERS
2023/7/1
The comparison of the clinical outcomes and costs between surgical aortic valve replacement and transcatheter aortic valve implantation based on the Japanese Diagnosis Procedure Combination database.
タグ:
DPC
2023/7/3
Impacts of routine varicella vaccination program and COVID-19 pandemic on varicella and herpes zoster incidence and health resource use among children in Japan.
タグ:
JMDC
2023/7/4
Disproportionality Analysis of Abemaciclib in the FDA Adverse Event Reporting System: A Real-World Post-Marketing Pharmacovigilance Assessment.
タグ:
FAERS
2023/7/7
Seizures associated with antibiotics: a real-world disproportionality analysis of FAERS database.
タグ:
FAERS
2023/7/7
Adverse events related to darolutamide treatment: analysis of “real life” data from EudraVigilance and the Food and Drug Administration database entries.
タグ:
EudraVigilance
FAERS
2023/7/6
Atypical femur fracture associated with common anti-osteoporosis drugs in FDA adverse event reporting system.
タグ:
FAERS
2023/7/6
Neuropsychiatric adverse reactions in patients treated with denosumab: two case reports and a review of data from the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2023/7/5
Urological complications after COVID 19 vaccine according to age, sex and manufacturer.
タグ:
VAERS
2023/7/4
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