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Participants 283 patients 65 years with VB12 deficiency were randomly assigned to oral (n=140) or IM (n=143) treatment arm
This study utilizes data from the FDA Adverse Event Reporting System (FAERS) to identify and compare adverse events (AEs) signals related to hepatobiliary disorders associated with triazole antifungal agents (TAAs), aiming to inform clinical selection and risk assessment of these drugs
Many labeled products specify storage at controlled room temperature (2025C)
