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Adverse Event Profiles of Adalimumab in Children: A Disproportionality Analysis.
タグ:
FAERS
2024/8/31
Mortality and Serious Adverse Events Associated With Glucagon-Like Peptide-1 Receptor Agonists: A Pharmacovigilance Study Using the FDA Adverse Event Reporting System.
タグ:
FAERS
2024/9/2
An analysis of the safety of Sevoflurane drugs: A disproportionality analysis based on Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2024/9/1
Prostaglandin analogues signal detection by data mining in the FDA Adverse Event Reporting System database.
タグ:
FAERS
2024/8/31
Exploring the correlation between cardiovascular adverse events and antidepressant use: A retrospective pharmacovigilance analysis based on the FDA Adverse Event Reporting System database.
タグ:
FAERS
2024/8/31
Association between age and onset of daptomycin-induced adverse events using the U.S. food and drug administration adverse event reporting system.
タグ:
FAERS
2024/8/31
Nuclear Receptors and Stress Response Pathways Associated with the Development of Oral Mucositis Induced by Antineoplastic Agents.
タグ:
FAERS
2024/8/31
Drug-induced liver injury associated with atypical generation antipsychotics from the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2024/8/31
What is the validity of the Federal Adverse Event Reporting System in contemporary clinical research?
タグ:
FAERS
2024/9/4
Antibody-drug conjugates-related interstitial lung diseases: data mining of the FAERS database.
タグ:
FAERS
2024/9/4
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