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no adverse event accumulation

Cox, Daniel Eichner Published: Drug Testing and Analysis, Volume 7, Issue 1, January 2015, pages 3138 DOI: 10.1002/dta.1715 URL: AOD9604 was incubated in human serum and rat plasma at room temperature to study in vitro metabolic degradation

Consequently, many research programs emphasize documentation, consistency, and quality-focused evaluation procedures throughout the research process

Limited human evidence: Human studies have mainly evaluated safety and metabolic markers

Follow-up labs help show whether the injection schedule is working

Chloramphenicol should be discontinued if anemia attributable to chloramphenicol is noted during periodic blood studies, which should be done approximately every 2 days during chloramphenicol receipt