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Abstract

A REVIEW ON ADVERSE DRUG REACTION

Neha Pharate*, Sushama Vidhate, Monika Ovol and Payal Kadus

Abstract

During the post-marketing phase of a drug's life cycle, pharmacovigilance is a practice aimed at monitoring drug safety in real-world situations and capturing adverse drug occurrences. Underreporting of adverse responses, on the other hand, is a major source of concern and a threat to pharmacovigilance systems. The current paper examines the key roadblocks to spontaneous reporting of adverse drug reactions (ADRs) in India, as well as potential alternatives. The biggest hurdles to ADR reporting, according to existing scientific research, include a lack of information and awareness among health professionals, physicians' attitudes regarding reporting, issues creating reporting systems in hospitals, and insufficient training to recognize ADRs. Pharmacovigilance also known as drug safety is defined as the science and activities relating to the collection, detection, assessment, monitoring, and prevention of adverse effects or any other drug related problems. The occurrence of ADR is a price the patient pays for the benefits increasinghealth care cost, modern medicine. Objective:- To study detailed information on Adverse Drug Reaction (ADR).

Keywords: Adverse drug Reaction it's type, mechanism, factor predisposing, affecting factor, ADR monitoring, management, detection, prevention etc.


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