Background A pharmacovigilance database of real-world adverse drug reaction (ADR)
reports is helpful for characterising adverse events and identifying new signals after drug …

The current study aimed to identify the crude drugs associated with drug-induced liver injury
(DILI) in 148 Kampo medicines prescribed throughout Japan using the Japanese Adverse …

Purpose: The goal of this study was to clarify the reporting patterns of self-reported adverse
drug reactions (ADRs) in China. Methods: A variety of sources were searched, including the …

Purpose This study aimed to assess the type, severity, seriousness, reasons, and outcomes
of adverse drug reactions (ADRs) in the reports submitted to the regional spontaneous ADR …

Reports on drug-related adverse reactions from manufacturing/distributing pharmaceutical
companies or medical institutions/pharmacies are regulated under the Pharmaceutical …

Drugs that damage the liver account for 9.5% of all suspected adverse drug reactions
(ADRs), are the main cause of fatal ADRs and are the most common reason for withdrawal …

Background The South African Health Products Regulatory Authority (SAHPRA) monitors
the safety of health products by collecting and evaluating adverse drug reaction (ADR) …

Drug-induced liver injury (DILI) is a type of bizarre adverse drug reaction (ADR) damaging
liver (L-ADR) which may lead to substantial hospitalizations and mortality. Due to the …

Background Spontaneous reporting on adverse drug reactions (ADR) has been established
in Malaysia since 1987, and although these reports are monitored by the Malaysia drug …

Objective: To evaluate the epidemiology of adverse drug reactions (ADRs) in the Korean
population and to identify their characteristics and factors affecting their severity. Materials …