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PD-1/PD-L1 inhibitors-associated cardiac adverse events: a retrospective and real-world study based on the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2023/4/19
COVID-19 Vaccine Safety First Year Findings in Adolescents.
タグ:
VAERS
FAERS
2023/4/21
Severe cutaneous adverse reactions to drugs: A real-world pharmacovigilance study using the FDA Adverse Event Reporting System database.
タグ:
FAERS
2023/4/21
Pharmacovigilance analysis of cardiac risks associated with Bruton tyrosine kinase inhibitors.
タグ:
FAERS
2023/4/19
Safety profile of clobazam in the real world: an analysis of FAERS database and systematic review of case reports.
タグ:
FAERS
2023/4/19
Adverse events related to alpha-blockers: analysis of real-life data from Eudra-Vigilance.
タグ:
EudraVigilance
2023/4/18
Evaluation of Cardiac Adverse Events with Ponatinib Using a Spontaneous Reporting Database.
タグ:
JADER
2023/4/20
Evaluating Ethnic Variations in the Risk of Infections in People With Prediabetes and Type 2 Diabetes: A Matched Cohort Study.
タグ:
CPRD
2023/4/13
Contextualising adverse events of special interest to characterise the baseline incidence rates in 24 million patients with COVID-19 across 26 databases: a multinational retrospective cohort study.
タグ:
CPRD
2023/4/11
Predicting the future risk of lung cancer: development, and internal and external validation of the CanPredict (lung) model in 19.67 million people and evaluation of model performance against seven other risk prediction models.
タグ:
CPRD
2023/4/9
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