Abstract
Background: Pharmacy professionals, other healthcare professionals, and patients can all gain from a continuous adverse drug reaction tracking and reporting strategy. The purpose of pharmacovigilance procedures is to collect information on various aspects of the safety of pharmaceutical goods in general. Patient, healthcare professional, and manufacturer reports are the main sources of information on adverse events that arise spontaneously. Pharmacovigilance is a requirement for all healthcare practitioners, making pharmacists and doctors essential healthcare providers in responsibility of adverse drug reaction reporting throughout their practices and teaching the general public about pharmacovigilance. The current study sought to investigate and evaluate the main causes of ADR underreporting.
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