Abstract

Drug-toxicology is a critical field in understanding and mitigating the risks associated with drug exposure. By evaluating the adverse effects of pharmaceuticals on biological systems, drug-toxicology plays a pivotal role in preventing drug-induced harm. Clinical toxicology, a subset of this field, focuses on diagnosing and managing toxic drug exposures in medical settings. Regulatory affairs ensure the implementation of safety protocols, standardizing drug approval processes and post-market surveillance. This article delves into the methodologies, findings, and implications of drug-toxicology, emphasizing its collaborative role in clinical applications and regulatory frameworks to ensure drug safety and public health protection.