Purpose To determine the incidence, demographic profile, background of reporters,
causative agents, severity and clinical outcomes of hepatic adverse drug reaction (ADR) …

Hepatic adverse drug reactions (ADRs) to certain drugs may differ within each country,
reflecting different patterns of prescription, socioeconomic status, and culture. The purpose …

Aim This study aimed to analyze the current trends of drug‐induced liver‐related adverse
events in the Food and Drug Administration Adverse Event Reporting System (FAERS) and …

Abstract Objective Adverse drug reactions (ADRs) can involve all tissues and organs. Liver
injuries are considered among the most serious and are a cause for concern among …

Purpose: To evaluate patient adverse drug reaction (ADR) reports in terms of categories by
System Organ Class (SOC), suspected products and seriousness. Methods: The national …

Purpose The main aim of this study was to determine the most frequently reported drugs to
the Serbian Pharmacovigilance Database (SPD) with suspected induced hepatotoxicity …

Abstract Background In Canada, adverse drug reaction (ADR) reporting was initiated in
1965. Since 2003, consumers have been able to report ADRs directly to Health Canada …

Background An adverse drug reaction (ADR) is a noxious and unintended response to a
drug which occurs at a normal therapeutic dose. Most non‐dose related ADR s remain …

Abstract Background Adverse drug reactions (ADRs) are a source of concern in healthcare
as they negatively affect patients. Serious adverse drug reactions (SADRs) have an even …

Objective To compare the risk of liver-related adverse drug reactions (ADRs) in children and
adults. Study design A case/non-case analysis on spontaneous reports based on the China …