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Characteristics of adverse drug reactions induced by flutamide and bicalutamide: a real-world pharmacovigilance study using FAERS.
タグ:
FAERS
2023/10/5
Post-marketing safety surveillance of dalfampridine for multiple sclerosis using FDA adverse event reporting system.
タグ:
FAERS
2023/10/2
Epirubicin and gait apraxia: a real-world data analysis of the FDA Adverse Event Reporting System database.
タグ:
FAERS
2023/10/2
Involvement of multiple cytochrome P450 isoenzymes in drug interactions between ritonavir and direct oral anticoagulants.
タグ:
FAERS
2023/10/2
Pharmacovigilance of unlicensed cannabidiol in European countries.
タグ:
EudraVigilance
2023/10/6
An expert review of clozapine in Eastern European countries: Use, regulations and pharmacovigilance.
タグ:
VigiBase
2023/10/3
Drug-induced immune hemolytic anemia: detection of new signals and risk assessment in a nationwide cohort study.
タグ:
VigiBase
2023/10/2
Benefit of prompt initiation of single-inhaler fluticasone furoate, umeclidinium, and vilanterol (FF/UMEC/VI) in patients with COPD in England following an exacerbation: a retrospective cohort study.
タグ:
CPRD
2023/9/26
Online Survey to Investigate Asthma Medication Prescription and Adherence from the Perspective of Patients and Healthcare Practitioners in England.
タグ:
CPRD
2023/9/25
Risk-stratified monitoring for thiopurine toxicity in immune-mediated inflammatory diseases: prognostic model development, validation, and, health economic evaluation.
タグ:
CPRD
2023/9/25
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