METHOD OF MONITORING ADVERSE DRUG REACTION IN PHARMACOVIGILANCE AND WHO INTERNATIONAL DRUG MONITORING PROGRAM
Deepak Shahu*, Sunil Kumar, K. Prabhu and Seema Saini
Abstract
Pharmacovigilance is the science and activities associated with
gathering, detection, identification and assessment of adverse event
data. The main aim of pharmacovigilance is to detect the risk factor of
drug and collect to convert in data providing form. In this we discuss
the various methods of detection of ADRs to save and secure the
patient from the noxious effect of the drug which may be life
threatening for him. Pharmaceutical industry in India leads the world at
3rd position for production of medicine by volume and at 13th position
in terms of value. Pharmaceutical industry in india grow due to their
Clinical research and Product development in which
pharmacovigilance play an important role for the safety purpose and
patient must be treated consistent with the requirements and illness of patient therefore the
utmost value is given to monitoring of patient safety levels of drug development which may
be dynamic process to achieve their approaches safety monitoring.
Keywords: Adverse drug reaction, Anecdotal, Record linkage & WHO monitoring.
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