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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
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
Subacute thyroiditis and COVID-19 vaccines: a case/non-case study.
タグ:
EudraVigilance
2022/6/10
Screening the European pharmacovigilance database for reports of clozapine-related DRESS syndrome: 47 novel cases.
タグ:
EudraVigilance
2022/6/1
Safety profile of hydroxychloroquine used off-label for the treatment of patients with COVID-19: A descriptive study based on EudraVigilance data.
タグ:
EudraVigilance
2022/5/9
Eosinophilia Induced by Blocking the IL-4/IL-13 Pathway: Potential Mechanisms and Clinical Outcomes.
タグ:
EudraVigilance
2022/5/7
Are finasteride-related penile curvature/Peyronie’s disease Adverse Event Reports worthy of further clinical investigation? Disproportionality analysis based on both the Food and Drug Administration (FDA) and the European Medicines Agency (EMA) pharmacovigilance databases.
タグ:
FAERS
EudraVigilance
2022/5/6
A Focus on Abuse/Misuse and Withdrawal Issues with Selective Serotonin Reuptake Inhibitors (SSRIs): Analysis of Both the European EMA and the US FAERS Pharmacovigilance Databases.
タグ:
EudraVigilance
2022/5/29
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