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Pharmacovigilance01:19

Pharmacovigilance

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Post-marketing surveillance is a critical component of pharmaceutical regulation, often uncovering unanticipated adverse drug reactions (ADRs) once a drug is widely used over an extended period.
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Pharmaceutical Poisoning: Potential Scenarios01:26

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Pharmaceutical poisoning can occur through various channels, impacting an estimated 2 million hospitalized patients in the U.S. annually with serious adverse drug responses. These scenarios encompass both therapeutic uses, such as drug toxicity, where even standard dosages can lead to severe central nervous system depression, and non-therapeutic exposures, including accidental ingestion by children, and environmental and occupational exposures.Unintentional poisonings often involve exploratory...
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Drug Discovery: Overview01:26

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Drug discovery is a multifaceted process involving extensive screening, testing, and optimization of lead compounds to identify potential new drugs for therapeutic use. It combines several approaches, including screening large numbers of natural products, chemical modification of known active molecules, identification of new drug targets, and rational design based on biological mechanisms and drug-receptor structure. These approaches are carried out in both academic research laboratories and...
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Drug Toxicity: Risk factors01:24

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Adverse Drug Reactions (ADRs) are potential complications that arise during pharmacotherapy, influenced by multiple risk factors. Age plays a significant role; both neonates and the elderly are at heightened risk due to their respective immature and diminished metabolic and elimination processes. Gender also impacts ADRs, with females experiencing a 1.5 to 1.7-fold greater risk than males, which may be linked to pharmacokinetic, pharmacodynamic, and hormonal differences. Notably, neonates, the...
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Drug Toxicity: Overview01:00

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Drug toxicity quantifies the harm a compound causes to an organism, varying by dose and potentially impacting whole systems or specific organs like the liver. Toxic reactions may arise from venomous insect or spider bites, with effects ranging from mild symptoms to severe outcomes such as brain damage or death. Common forms of acute poisoning include ethanol intoxication and overdose of pain or fever medications, with substances like GHB and heroin being particularly lethal at doses close to...
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Drug toxicity: Idiosyncratic Reactions01:16

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Idiosyncratic drug reactions represent abnormal chemical responses that vary significantly among individuals, ranging from extreme sensitivity to low doses to insensitivity to high doses. These reactions often occur due to the drug's covalent binding with serum proteins, forming a foreign hapten that triggers an immunotoxicological response. The variability in drug reactions has a strong pharmacogenetic foundation, with genetic differences crucial in how individuals metabolize drugs. For...
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Using Literature-Based Discovery to Explain Adverse Drug Effects.

Dimitar Hristovski1, Andrej Kastrin2, Dejan Dinevski3

  • 1Institute for Biostatistics and Medical Informatics, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia. dimitar.hristovski@mf.uni-lj.si.

Journal of Medical Systems
|June 20, 2016
PubMed
Summary

Literature-based discovery (LBD) aids in explaining adverse drug effects by identifying linking genes or proteins. This research uses LBD to generate novel hypotheses for drug-induced adverse events.

Keywords:
Adverse drug effectsAdverse drug reactionsLiterature-based discoveryPharmacogenomicsPharmacovigilanceText mining

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Area of Science:

  • Pharmacology
  • Genomics
  • Biomedical Informatics

Background:

  • Adverse drug effects pose significant challenges in patient care and drug development.
  • Understanding the molecular mechanisms underlying adverse drug effects is crucial for drug safety.

Purpose of the Study:

  • To apply literature-based discovery (LBD) for generating pharmacological and pharmacogenomic explanations of adverse drug effects.
  • To identify genes or proteins that link drugs to their reported adverse effects, thereby elucidating causal pathways.

Main Methods:

  • Utilizing LBD to systematically analyze scientific literature and relevant databases.
  • Developing a method to identify molecular entities (genes/proteins) connecting drugs with adverse events.
  • Hypothesis generation through literature mining and data integration.

Main Results:

  • The LBD approach successfully identified potential molecular links between drugs and adverse effects.
  • Initial findings suggest the method's capability in uncovering mechanisms of drug toxicity.
  • The identified genes/proteins offer insights into the biological processes underlying adverse drug reactions.

Conclusions:

  • Literature-based discovery is a promising strategy for explaining adverse drug effects.
  • This research demonstrates the potential of LBD in advancing pharmacovigilance and drug safety research.
  • The identified molecular links can inform future research on drug-induced toxicity.