Publication: Drugs Associated with Hepatotoxicity and their Reporting Frequency of Liver Adverse Events in VigiBase (TM) Unified List Based on International Collaborative Work
dc.contributor.author | Suzuki, Ayako | |
dc.contributor.author | Andrade Bellido, Raul Jesús | |
dc.contributor.author | Bjornsson, Einar | |
dc.contributor.author | Lucena González, María Isabel | |
dc.contributor.author | Lee, William M | |
dc.contributor.author | Yuen, Nancy A | |
dc.contributor.author | Hunt, Christine M | |
dc.contributor.author | Freston, James W | |
dc.contributor.authoraffiliation | [Suzuki,A] Division of Gastroenterology, Duke University, Durham, North Carolina, USA. [Andrade Bellido,RJ] Unidad de Hepatología (Hepatology Unit), Grupo de Estudio para las Hepatopatías Asociadas a Medicamentos, Coordinating Center, Hospital Universitario Virgen de la Victoria, Facultad de Medicina, Campus Universitario de Teatinos, Malaga, Spain. [Bjornsson,E] Department of Internal Medicine, Section of Gastroenterology and Hepatology, Landspitali University Hospital, Reykjavik, Iceland. [Andrade Bellido,RJ; Lucena González,MI] Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Málaga, Spain. [Lucena González,MI] Servicio de Farmacología Clínica (Clinical Pharmacology Service), Grupo de Estudio para las Hepatopatías Asociadas a Medicamentos, Coordinating Center, Hospital Universitario Virgen de la Victoria, Facultad de Medicina, Campus Universitario de Teatinos, Málaga, Spain. [Lee,WM] Division of Digestive and Liver Diseases, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas, USA. [Yuen,NA; Hunt,CM] Global Clinical Safety and Pharmacovigilance, GlaxoSmithKline, Durham, North Carolina, USA. [Freston,JW] Department of Internal Medicine, University of Connecticut, Farmington, Connecticut, USA. | es |
dc.contributor.funder | This study has been partially funded by a research grant from the Spanish Medicine Agency, Fondo de Investigacion Sanitaria FIS PI 07/0980 and EC07/90910, and received support from Boehringer-Ingelheim. CIBERehd is funded by Instituto de Salud Carlos III. The ALF Study Group is funded by NIH Grant U-01 DK058369. | |
dc.date.accessioned | 2012-10-26T11:50:13Z | |
dc.date.available | 2012-10-26T11:50:13Z | |
dc.date.issued | 2010-06-01 | |
dc.description | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; | es |
dc.description.abstract | BACKGROUND Challenges exist in the clinical diagnosis of drug-induced liver injury (DILI) and in obtaining information on hepatotoxicity in humans. OBJECTIVE (i) To develop a unified list that combines drugs incriminated in well vetted or adjudicated DILI cases from many recognized sources and drugs that have been subjected to serious regulatory actions due to hepatotoxicity; and (ii) to supplement the drug list with data on reporting frequencies of liver events in the WHO individual case safety report database (VigiBase). DATA SOURCES AND EXTRACTION (i) Drugs identified as causes of DILI at three major DILI registries; (ii) drugs identified as causes of drug-induced acute liver failure (ALF) in six different data sources, including major ALF registries and previously published ALF studies; and (iii) drugs identified as being subjected to serious governmental regulatory actions due to their hepatotoxicity in Europe or the US were collected. The reporting frequency of adverse events was determined using VigiBase, computed as Empirical Bayes Geometric Mean (EBGM) with 90% confidence interval for two customized terms, 'overall liver injury' and 'ALF'. EBGM of >or=2 was considered a disproportional increase in reporting frequency. The identified drugs were then characterized in terms of regional divergence, published case reports, serious regulatory actions, and reporting frequency of 'overall liver injury' and 'ALF' calculated from VigiBase. DATA SYNTHESIS After excluding herbs, supplements and alternative medicines, a total of 385 individual drugs were identified; 319 drugs were identified in the three DILI registries, 107 from the six ALF registries (or studies) and 47 drugs that were subjected to suspension or withdrawal in the US or Europe due to their hepatotoxicity. The identified drugs varied significantly between Spain, the US and Sweden. Of the 319 drugs identified in the DILI registries of adjudicated cases, 93.4% were found in published case reports, 1.9% were suspended or withdrawn due to hepatotoxicity and 25.7% were also identified in the ALF registries/studies. In VigiBase, 30.4% of the 319 drugs were associated with disproportionally higher reporting frequency of 'overall liver injury' and 83.1% were associated with at least one reported case of ALF. CONCLUSIONS This newly developed list of drugs associated with hepatotoxicity and the multifaceted analysis on hepatotoxicity will aid in causality assessment and clinical diagnosis of DILI and will provide a basis for further characterization of hepatotoxicity. | es |
dc.description.version | Yes | es |
dc.identifier.citation | Suzuki A, Andrade RJ, Bjornsson E, Lucena MI, Lee WM, Yuen NA, et al. Drugs associated with hepatotoxicity and their reporting frequency of liver adverse events in VigiBase: unified list based on international collaborative work. Drug Saf. 2010 ; 33(6):503-22 | es |
dc.identifier.doi | 10.2165/11535340-000000000-00000 | |
dc.identifier.essn | 0114-5916 | |
dc.identifier.issn | 1179-1942 | |
dc.identifier.pmid | 20486732 | |
dc.identifier.uri | http://hdl.handle.net/10668/588 | |
dc.journal.title | Drug safety : an international journal of medical toxicology and drug experience | |
dc.language.iso | en | |
dc.publisher | ADIS INT LTD | es |
dc.relation.publisherversion | http://adisonline.com/drugsafety/pages/articleviewer.aspx?year=2010&issue=33060&article=00007&type=abstract | es |
dc.rights.accessRights | open access | |
dc.subject | Liver damage | es |
dc.subject | Prescription Drugs | es |
dc.subject | Toxicidad de Medicamentos | es |
dc.subject.mesh | Medical Subject Headings::Health Care::Health Services Administration::Organization and Administration::Pharmacy Administration::Drug and Narcotic Control | es |
dc.subject.mesh | Medical Subject Headings::Diseases::Substance-Related Disorders::Poisoning::Drug-Induced Liver Injury | es |
dc.subject.mesh | Medical Subject Headings::Geographicals::Geographic Locations::Europe | es |
dc.subject.mesh | Medical Subject Headings::Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans | es |
dc.subject.mesh | Medical Subject Headings::Disciplines and Occupations::Social Sciences::Internationality::International Cooperation | es |
dc.subject.mesh | Medical Subject Headings::Chemicals and Drugs::Pharmaceutical Preparations::Prescription Drugs | es |
dc.subject.mesh | Medical Subject Headings::Health Care::Health Services Administration::Organization and Administration::Pharmacy Administration::Drug and Narcotic Control::Safety-Based Drug Withdrawals | es |
dc.subject.mesh | Medical Subject Headings::Geographicals::Geographic Locations::Americas::North America::United States | es |
dc.subject.mesh | Medical Subject Headings::Health Care::Health Care Economics and Organizations::Organizations::International Agencies::United Nations::World Health Organization | es |
dc.subject.mesh | Medical Subject Headings::Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Evaluation Studies as Topic::Product Surveillance, Postmarketing::Adverse Drug Reaction Reporting Systems | es |
dc.title | Drugs Associated with Hepatotoxicity and their Reporting Frequency of Liver Adverse Events in VigiBase (TM) Unified List Based on International Collaborative Work | es |
dc.type | research article | |
dc.type.hasVersion | VoR | |
dspace.entity.type | Publication |
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