Abstract

Adverse drug reactions are completely unwanted drug reactions derived from self-medications and among those unpleasant reactions, severe cutaneous adverse drug reactions like, Stevens-Johnson Syndrome, Toxic Epidermal Necrolysis, Acute Generalized Exanthematous Pustolosis and Drug Reaction with Eosinophilia and Systemic Symptoms, are mostly life threatening harms, globally. The main objective of this study was to find out the impact of early detection of the adverse drug events and consequently prompt withdrawn of the suspected culprit drugs in the ultimate survival rate among the patients experienced with these types of unwelcome life threatening events in Bangladesh. Here, we found that antibiotics were accounted for most adverse drug reactions (81.13%, n=53) including serious reactions. This study also showed that if the adverse drug event is possibly detected with in the first 48 hours then, 72.73% (n=11) patients were survived from severe cutaneous adverse drug reactions, where as if delayed than 48 hours, only 20% (n=5) patients were survived. Similarly, 77.77% (n=9) patients were survived after the proper treatment when suspected culprit drugs were discontinued within first 48 hours and late discontinuation resulted in only 28.57% (n=7) survival rate among these patients. So, prompt response through early event-detection and discontinuation of the culprit drug, to a serious cutaneous adverse drug reaction can tremendously save life by providing early necessary management and required treatment.

Highlights

  • An adverse drug event (ADE) can be defined as an injury resulting from medical intervention related to a drug (Kohn et al 2000)

  • The main aim of this study was to find out the impact of early detection of adverse drug reaction (ADR) with a fast initiative to take the victim under necessary treatment at hospital settings, and the affect of undelayed discontinuation of the culprit drug in severe ADRs in Bangladesh

  • Total 53 (n) ADRs were found during that selected time and analyzed (Table 1). 43 (81.13%, n=53) reports were found against antibiotics; 3 (5.66%, n=53) reports against ketorolac under NSAID and 3 (5.66%, n=53) reports against paracetamol under antipyretic/analgesic were found (Table 1)

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Summary

Introduction

An adverse drug event (ADE) can be defined as an injury resulting from medical intervention related to a drug (Kohn et al 2000). An adverse drug reaction (ADR) is a medication-induced injury. ADR can be defined as a noxious, unpleasant or unwanted reaction resulting from a medicinal intervention at a regular dose used in human in order to prophylaxis, diagnosis or therapy (Aronson et al 2005; World health organization, 2003). ADRs can be broadly classified into two groups- type A (predictable reactions, usually dose-dependent) and type B (unpredictable or idiosyncratic, and not dosedependent). Other short classifications are type C (chronic, depends on dose and time); type D (delayed reaction); type E (end of use reactions that cover withdrawals) and type F (failure of therapy) (Coleman et al 2016)

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