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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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Effects of Chemicals: Overview01:27

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Drugs, encompassing various chemical compounds from natural sources, lab synthesis, or genetic engineering, elicit different biological responses in living organisms. Some of these responses are desirable or therapeutic, while others are undesirable. The primary goal of administering a drug is to achieve a therapeutic effect, that is, to address a specific disease or health condition. Any concurrent effects outside of this therapeutic outcome are considered undesirable. These undesirable...
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When drugs are administered, they can elicit either an agonist or antagonist effect on the body. Agonism occurs when a drug activates a specific receptor, triggering a biological response. On the other hand, antagonism happens when a drug binds to the same receptors but blocks their activation, thereby preventing a biological response.
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Drug interactions occur when the pharmacological effect of one drug is altered by another substance, either enhancing or diminishing its activity. The drug whose activity is altered is known as the object drug, and the substance causing the alteration is called the agent drug or the precipitant. The net effects of these interactions are mostly undesirable, leading to decreased effectiveness or increased adverse effects. In rare cases, interactions can be beneficial, such as the enhanced...
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Therapeutic Drug Monitoring: Affecting Factors01:29

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Therapeutic Drug Monitoring (TDM) is the clinical practice of measuring specific drug levels in a patient's blood or body tissues to manage and optimize therapy. TDM is crucial for drugs with narrow therapeutic windows, like warfarin and phenytoin, where incorrect doses can lead to treatment failure or severe side effects. This monitoring ensures the dosage administered is within a safe and effective range. The factors affecting therapeutic drug monitoring include:Patient-Specific Factors:a.
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Combined Effects of Drugs: Antagonism01:30

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The combined effects of drugs can result in various interactions, of which an important type is antagonism. Antagonism is a mechanism where one drug inhibits or counteracts the effects of another drug. Antagonism can occur through various means, including receptor binding, allosteric modulation, functional interaction, chemical reactions, and pharmacokinetic processes.
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Updated: Jan 8, 2026

Evidence-based Knowledge Synthesis and Hypothesis Validation: Navigating Biomedical Knowledge Bases via Explainable AI and Agentic Systems
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Causal knowledge graph analysis identifies adverse drug effects.

Sumyyah Toonsi1, Paul N Schofield2, Robert Hoehndorf1,3,4

  • 1Computer, Electrical and Mathematical Sciences & Engineering Division, King Abdullah University of Science and Technology, Thuwal 23955, Saudi Arabia.

Bioinformatics (Oxford, England)
|December 12, 2025
PubMed
Summary
This summary is machine-generated.

We introduce Causal Knowledge Graphs (CKGs) to combine biomedical knowledge graphs with causal inference. This approach successfully identified known and novel adverse drug effects, improving drug indication prediction.

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Area of Science:

  • Biomedical Informatics
  • Causal Inference
  • Knowledge Representation

Background:

  • Biomedical knowledge graphs and causal models are valuable but disconnected.
  • Knowledge graphs lack probabilistic semantics; causal models lack background knowledge integration.

Purpose of the Study:

  • To bridge the gap between knowledge graphs and causal models.
  • To develop Causal Knowledge Graphs (CKGs) for principled causal inference and hypothesis formulation.

Main Methods:

  • Extended knowledge graphs with formal causal semantics, creating Causal Knowledge Graphs (CKGs).
  • Constructed a Drug-Disease CKG (DD-CKG) integrating disease pathways, drug indications, and side effects.
  • Applied DD-CKG to UK Biobank and MIMIC-IV for large-scale mediation analysis of drug effects.

Main Results:

  • CKGs enabled deconfounding and hypothesis formulation using background knowledge.
  • Successfully reproduced known adverse drug reactions and identified novel candidate effects.
  • Improved prediction of shared drug indications by combining predicted effects with existing databases.

Conclusions:

  • CKGs provide a generalizable, knowledge-driven framework for scalable causal inference.
  • The methodology demonstrates clinical relevance and supports automated large-scale mediation analysis.
  • This approach enhances understanding of drug effects and disease progression.