国际药学与生命科学研究与发展杂志

抽象的

Pharmacovigilance and Clinical Safety: Comparison between India, US and Europe-A Review

Dr. Amirtha Tom, Rhea Joseph, Priyanka Pingat, Dr.Harinarayanan

Pharmacovigilance (PV) is a crucial component of the system for regulating pharmaceuticals. PV is essential for the detection, evaluation, and dissemination of adverse drug reactions (ADRs) using a variety of channels. ADRs cause significant harm to patients and can possibly increase morbidity and mortality. The public health safety and promotion of responsible drug use are both aided by the PV databases. In order to broaden the scope of the current PV structure in India, this essay analyzes the PV systems in the USA, Europe, and India while underlining the difficulties and potential solutions. In comparison to other nations, PV schemes in India are still in their infancy.