Nadda said that drug safety related issues pose a major challenge for healthcare professionals, regulators and pharmaceuticals industry and this is where Pharmacovigilance, the monitoring of adverse effects of drugs, plays a significant role in ensuring quality and efficacy of medical products.
He was addressing the 38th Annual Meeting of Representatives of the National Pharmacovigilance Centres participating in the WHO Programme for International Drug Monitoring, jointly organised by IPC and WHO.
"Considerable progress has been made by the India Pharmacovigilance Programme over the last few years, including setting up of pharmacovigilance system in tuberculosis and HIV-AIDS related public health programmes," he said, after inaugurating the 38th annual meeting of National Pharmacovigilance Centres.
Launched in 2010, the pharmacovigilance programme has set up 179 centres across the county.
Adverse drug reactions are reported to Indian Pharmacopoeia Commission, which works in collaboration with global Adverse Drug Reaction Monitoring Centre, Sweden to contribute to the global Adverse Drug Reactions data base, Nadda said.
"People prescribe medicines from across the border through internet and all kinds of medicines are coming for which we are not sure whether they are fully tested. They might be coming from places which may not be having a strong regulatory system. People are also taking self-medication, then there also counterfeit and substandard medication also. In such situation the need for a pharmacovigilance system is very important," Sharma said.
Aim of the meeting was to provide a platform to representatives of Pharmacovigilance Centres from around the world to meet and discuss on co-vigilance and drug safety issues.
