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Related Concept Videos

Drug toxicity: Idiosyncratic Reactions01:16

Drug toxicity: Idiosyncratic Reactions

195
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...
195
Drug Toxicity: Allergic Reactions01:30

Drug Toxicity: Allergic Reactions

154
Drug-related allergies are immune-mediated responses triggered by the administration of pharmacological agents. These hypersensitivity reactions are classified based on the immune mechanisms involved. The four primary types—Type I, II, III, and IV—are mediated by different immunological pathways and exhibit distinct clinical manifestations.Type I Hypersensitivity/ IgE-Mediated Reactions: Immunoglobulin E (IgE) immediately mediates Type I hypersensitivity reactions. Upon initial...
154
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.
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
2.0K
Allergic Drug Reactions01:27

Allergic Drug Reactions

1.6K
Allergic reactions related to drugs are hypersensitivity responses driven by the immune system and bear no connection to the drug's therapeutic action. While drugs in isolation do not trigger an immune response, they can interact with endogenous proteins to form antigens. These antigens stimulate lymphocytes to produce antibodies. IgE-type antibodies attach themselves to mast cells. Upon subsequent exposure to the same stimulus, the antigen-antibody interaction is initiated, unleashing...
1.6K
Drug Toxicity: Risk factors01:24

Drug Toxicity: Risk factors

206
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...
206
Drug Toxicity: Overview01:00

Drug Toxicity: Overview

223
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...
223

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High-throughput and Comprehensive Drug Surveillance Using Multisegment Injection-Capillary Electrophoresis-Mass Spectrometry
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New and Emerging Drug Reactions.

Emily Y Chu1, Jonathan L Curry2, Cuong V Nguyen3

  • 1Department of Dermatology & Pathology and Laboratory Medicine, Hospital of the University of Pennsylvania, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Dermatologic Clinics
|April 8, 2026
PubMed
Summary
This summary is machine-generated.

Newer medications for inflammatory skin diseases and cancer can cause skin reactions. This article reviews the clinical and histopathologic findings of these cutaneous adverse events, aiding in diagnosis and management.

Keywords:
BiologicCutaneous adverse reactionDrug reactionImmune checkpoint inhibitorSmall molecule inhibitorTargeted therapy

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Area of Science:

  • Dermatology
  • Oncology
  • Pharmacology

Background:

  • Novel therapeutic agents are increasingly utilized for inflammatory skin conditions and oncologic indications.
  • Understanding the spectrum of cutaneous adverse reactions associated with these medications is crucial for patient care.
  • Recent approvals include dupilumab, IL-12/-23 and IL-23 inhibitors, immune checkpoint inhibitors, mogamulizumab, and enfortumab vedotin.

Purpose of the Study:

  • To review the clinical and histopathologic findings of cutaneous adverse reactions to newer medications.
  • To provide a comprehensive overview of skin toxicities associated with targeted therapies for dermatologic and oncologic conditions.

Main Methods:

  • Review of clinical presentations and histopathologic features.
  • Synthesis of data from recent literature and clinical experience.
  • Focus on specific drug classes including biologics and targeted cancer therapies.

Main Results:

  • Diverse cutaneous adverse reactions are associated with dupilumab, IL-12/-23 and IL-23 inhibitors, immune checkpoint inhibitors, mogamulizumab, and enfortumab vedotin.
  • Specific patterns of skin toxicity are observed for each medication class.
  • Histopathologic findings aid in differentiating drug-induced reactions from underlying diseases.

Conclusions:

  • Early recognition and accurate diagnosis of drug-induced cutaneous reactions are essential.
  • Awareness of these adverse events facilitates appropriate management and minimizes morbidity.
  • This review serves as a resource for clinicians managing patients on novel systemic therapies.