Adverse Drug Reactions (ADRs) are a major concern in clinical practice and significantly contribute to morbidity and mortality worldwide [1]. Pharmacovigilance plays a crucial role in detecting, assessing, and preventing ADRs [2]. In India, the Pharmacovigilance Programme of India (PvPI) has been established to monitor drug safety [3]. However, underreporting remains a major challenge due to lack of awareness and inadequate training [4].