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10 de ene. de 2024 · An adverse drug reaction (ADR) refers to an untoward reaction to a medication. ADRs are common and constitute a significant healthcare burden. The most robust database of ADRs available is the U.S. Food and Drug Administration's Adverse Event Reporting System (FAERS).
Learn about the causes, symptoms, diagnosis, treatment, and prevention of adverse drug reactions (ADRs), also known as side effects or adverse drug effects. Find out the risk factors, classification, and treatment options for different types of ADRs, such as dose-related, allergic, and idiosyncratic.
7 de oct. de 2000 · We define an adverse drug reaction as "an appreciably harmful or unpleasant reaction, resulting from an intervention related to the use of a medicinal product, which predicts hazard from future administration and warrants prevention or specific treatment, or alteration of the dosage regimen, or withdrawal of the product."
An adverse drug reaction (ADR) is a harmful, unintended result caused by taking medication.: 1.1 Adverse Drug Reaction (ADR) ADRs may occur following a single dose or prolonged administration of a drug or may result from the combination of two or more drugs.
This article reviews the key facts and aspects of adverse drug reactions (ADRs) in clinical practice, such as their definition, classification, causes, prevention and reporting. It also discusses the role of pharmacogenetics and pharmacovigilance in reducing the risk of ADR-related harm and improving patient safety.
