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Second primary malignancies after commercial CAR T-cell therapy: analysis of the FDA Adverse Events Reporting System.
タグ:
FAERS
2024/3/14
Delta-8, a Cannabis-Derived Tetrahydrocannabinol Isomer: Evaluating Case Report Data in the Food and Drug Administration Adverse Event Reporting System (FAERS) Database.
タグ:
FAERS
2023/2/7
Otolaryngologic Side Effects After COVID-19 Vaccination.
タグ:
VAERS
FAERS
2023/8/4
Co-occurring infections in cancer patients treated with checkpoint inhibitors significantly increase the risk of immune related adverse events.
タグ:
FAERS
2024/2/26
Validation of the newly proposed Brighton Collaboration case definition for vaccine-induced immune thrombocytopenia and thrombosis.
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VAERS
FAERS
2024/7/14
Hemophagocytic lymphohistiocytosis induced by dabrafenib-trametinib in a patient with metastatic melanoma: a case report and pharmacovigilance analysis.
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FAERS
2024/7/22
Disproportionality analysis of data from VigiBase and other global product safety databases on toxicity of iron chelating agents.
タグ:
VigiBase
FAERS
2024/7/29
Pediatric drug-induced anaphylaxis reports in the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2024/6/4
Immune Checkpoint Inhibitors-Associated Diabetes and Ketoacidosis Were Found in FDA Adverse Event Reporting System: A Real-World Evidence Database Study.
タグ:
FAERS
2024/6/15
Mining of neurological adverse events associated with valbenazine: A post-marketing analysis based on FDA adverse event reporting system.
タグ:
FAERS
2024/6/21
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