Pharmacovigilance - A Global System of Monitoring ADRs

  • Dr Rakesh Chaurasiya
Keywords: Haemovigilance, Materiovigilance, Biovigilance, Teratogenicity, Vigiflow

Abstract

No drug is safe. Every drug has the potential to develop minor to life threatening adverse effects. Adverse Drug Reactions (ADRs) are one of the major causes of morbidity & mortality worldwide. It adds economic burden to healthcare. Pharmacovigilance is the science dealing with activities related to detection, assessment, understanding and prevention of adverse reactions or any other possible medicine related problem.

Pharmacovigilance has an important role in rational use of medicine, as it provides the basis for assessing safety of medicine in the community. Its International Center is situated in Uppsala, Sweden. Pharmacovigilance Program of India (PvPI) started since 2011. India is major contributor participating in WHO international drug monitoring. PvPI is now expanded and incorporated with RNTCP & NACO. Haemovigilance, Materiovigilance, AEFI & Biovigilance are additional programmes.

References

1. Guidance document for spontaneous adverse drug reaction reporting: Published by Indian Pharmacopoeia Commission; Ministry of Health & Family Welfare, Government of India; 2014.
2. Classification of ADRs: P.V Rataboli; Clinical Pharmacology & Rational Therapeutics;459 -460;2007.
3. News Letters: Published by NCC-PvPI, Indian Pharmacopoeia Commission; Ministry of Health & Family Welfare , Government of India ; Vol 5, Issue 12, 2015.
Published
2019-07-08
How to Cite
Dr Rakesh Chaurasiya. (2019). Pharmacovigilance - A Global System of Monitoring ADRs. The Indian Practitioner, 69(12), 32-36. Retrieved from https://articles.theindianpractitioner.com/index.php/tip/article/view/343