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The FDA Adverse Event Reporting System (FAERS) is a comprehensive database of ADRs specifically designed by the FDA to facilitate postmarketing surveillance of drugs and therapeutic biologics [19]
ICA69 aggravates ferroptosis causing septic cardiac dysfunction via STING trafficking
Qsymia (phentermine/topiramate) Approved - A combination medication that suppresses appetite and enhances feelings of fullness
Klyachko, A.V
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