Indian Journal of Anaesthesia  
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SPECIAL ARTICLE
Year : 2017  |  Volume : 61  |  Issue : 7  |  Page : 534-537

Safety monitoring of local anaesthetic drugs from the perspective of Pharmacovigilance Programme of India


Indian Pharmacopoeia Commission, Ministry of Health and Family Welfare, Government of India Ghaziabad, Uttar Pradesh, India

Correspondence Address:
Ismeet Kaur
Indian Pharmacopoeia Commission, Sector 23, Rajnagar, Ghaziabad - 201 002, Uttar Pradesh
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ija.IJA_418_17

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Pharmacovigilance Programme of India (PvPI) was established to promote patient safety by the Ministry of Health and Family Welfare, Government of India in July 2010. It covers various medical hospitals/institutes and National Health Programmes across the country. India is coordinating with various national and international programmes to be a part of international drug monitoring and to monitor the risk-benefit profile of medicines. At present, India has contributed more than 200,000 adverse drug reactions (ADRs) to the database and can draw signals for regulatory decisions. To foster the culture of spontaneous reporting, India has launched paperless and simple modes of reporting ADRs such as Helpline and an Android application. This will help to create a national centre of excellence at par with global drug safety monitoring standards. With the increasing popularity of regional anaesthesia, adverse events may occur due to local anaesthetic drugs, techniques and adjuvants. Uncommon but clinically significant ADRs can be identified in a nationwide pharmacovigilance programme. Anaesthesiologists in India are encouraged to report local anaesthesia-related ADRs to the national pharmacovigilance database.


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