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Analysis of pharmacovigilance databases for spontaneous reports of adverse drug reactions related to substandard and falsified medical products: A descriptive study.
タグ:
FAERS
EudraVigilance
2022/9/24
Myelodysplastic Syndrome/Acute Myeloid Leukemia Following the Use of Poly-ADP Ribose Polymerase (PARP) Inhibitors: A Real-World Analysis of Postmarketing Surveillance Data.
タグ:
FAERS
EudraVigilance
2022/7/6
Reported congenital malformations after exposure to non-tumour necrosis factor inhibitor biologics: A retrospective comparative study in EudraVigilance.
タグ:
EudraVigilance
2022/7/28
Systematic review of spontaneous reports of myocarditis and pericarditis in transplant recipients and immunocompromised patients following COVID-19 mRNA vaccination.
タグ:
EudraVigilance
VAERS
2022/7/2
Comparative assessment of myocarditis and pericarditis reporting rates related to mRNA COVID-19 vaccines in Europe and the United States.
タグ:
EudraVigilance
2022/7/12
Pharmacovigilance Signals of the Opioid Epidemic over 10 Years: Data Mining Methods in the Analysis of Pharmacovigilance Datasets Collecting Adverse Drug Reactions (ADRs) Reported to EudraVigilance (EV) and the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
EudraVigilance
2022/6/25
European Safety Analysis of mRNA and Viral Vector COVID-19 Vaccines on Glucose Metabolism Events.
タグ:
EudraVigilance
2022/6/25
Adverse events related to antimuscarinics and beta-3-agonist: “real-life” data from the Eudra-Vigilance Database.
タグ:
EudraVigilance
2022/6/17
Risk of hepatitis B virus reactivation following treatment with abatacept: A retrospective study of international pharmacovigilance databases.
タグ:
FAERS
EudraVigilance
2022/6/17
Allergic Reactions to COVID-19 Vaccines: Risk Factors, Frequency, Mechanisms and Management.
タグ:
EudraVigilance
VigiBase
2022/6/14
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