Abstract

A REVIEW ON ADVERSE DRUG REACTION REPORTING MANAGEMENT FROM AN ALLERGIC PATIENT TO FINAL AUTHORITY

Manorama Ratre*

ABSTRACT

Now day’s pharmacy still growing in field of research, manufacturing, modification and dispensing of drugs. But another phase is that ADRs (Adverse drug reactions) also become cause of mortality today. So a proper channel should be required for all professionals to know how to manage the ADR report. When any ADRs occurs to any patient then the first responsibility is that the concerned people like patient attendee, nurse, consultant, pharmacist or any people to report the all over event (i. e. Patient detail, adverse event, caused medicine detail, other concomitant medicines, levels of ADRs etc) to proper authorized person. Then they report it within 24hrs to AMC (may be peripheral< regional< zonal) then report forwarded to NCC. Any person may also report directly to the NCC. In India PvPI, CDSCO (IDA- recommended renaming by DTAB) may help in reporting. In which some higher authentic medical colleges like AIIMS Delhi are playing for review the all data. Then finally report sends to WHO-UMC roles as International drug monitoring, situated at Sweden. UMC helps to provide the all data base to the WHO, this data also called vigibase and that data used by WHO for making data base network which helpful in Pharmacovigilance Monitoring. The overall conclusion is that for the purpose of safety of drug products, lowering the risk to the patients due to ADRs and awareness in people for prevent and cure such types of problem caused by a drug.

Keywords: AMC (ADRs Monitoring Centre), NCC (National Coordination Centre), PvPI (Pharmacovigilance Program in India), CDSCO (Central Drugs Standard Control Organization), DTAB (Drug Technical Advisory Board), WHO-UMC (World Health Organization-Upssala Monitoring C