Pharmacovigilance Programme of India: Recent developments and future perspectives

被引:33
|
作者
Kalaiselvan, Vivekanandan [1 ]
Thota, Prasad [1 ]
Singh, Gyanendra Nath [2 ]
机构
[1] Minist Hlth & Family Welf, Indian Pharmacopoeia Commiss, Pharmacovigilance Programme India, Coordinat Ctr, Ghaziabad, Uttar Pradesh, India
[2] Minist Hlth & Family Welf, Pharmacovigilance Programme India, Indian Pharmacopoeia Commiss, Ghaziabad, Uttar Pradesh, India
关键词
Adverse drug reaction reporting; patient safety; Pharmacovigilance Programme of India; ADVERSE DRUG-REACTIONS; EVENTS; COST;
D O I
10.4103/0253-7613.194855
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Promoting safe use of medicines is a priority of Indian Pharmacopoeia Commission that functions as the National Coordination Center (NCC) for Pharmacovigilance Programme of India (PvPI). One hundred and seventy-nine adverse drug reactions (ADRs) monitoring centers currently report ADRs to NCC. Current India contribution to global safety database reaches 3% and the completeness score is 0.93 out of 1. NCC is taking several measures to enhance patient safety including capacity building for monitoring, surveillance, collaboration with national health programs and other organizations to increase ADR reporting and to ensure that PvPI is a vital knowledge database for Indian regulators. The Central Drugs Standard Control Organization has notified important safety label changes on drugs such as carbamazepine and piperacillin + tazobactam in the year 2015, other drugs are under monitoring for regulatory interventions.
引用
收藏
页码:624 / 628
页数:5
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