Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Drug Toxicity: Allergic Reactions01:30

Drug Toxicity: Allergic Reactions

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 exposure to a...
Anticholinesterase Agents: Poisoning and Treatment01:26

Anticholinesterase Agents: Poisoning and Treatment

Anticholinesterases, also known as cholinesterase inhibitors, work by blocking the breakdown of acetylcholine, leading to its accumulation in the synaptic cleft. This accumulation indirectly enhances both muscarinic and nicotinic actions. These agents are classified as reversible or irreversible based on their mechanism of action.     
Irreversible agents form a strong bond with the cholinesterase enzyme, making it inactive. The breakdown of the phosphorylated enzyme is slower than the...
Drug Toxicity: Dose-Dependent Reactions01:24

Drug Toxicity: Dose-Dependent Reactions

Drug toxicities can be stratified into pharmacological, pathological, or genotoxic based on their mechanisms. The incidence and severity of these toxicities generally increase with the drug's concentration in the body and exposure time.Pharmacological toxicity is evident when the therapeutic effects of drugs overshoot into adverse reactions in a predictable, dose-dependent manner. Central nervous system (CNS) depression from barbiturates is a classic example, with effects escalating from...
Toxic Reactions: Overview01:26

Toxic Reactions: Overview

When toxic substances penetrate the human body, they disseminate to various tissues, undergoing metabolic changes. This process yields reactive metabolites that may covalently bind with specific target molecules, resulting in toxicity.
Toxicity falls into two primary categories: local and systemic.
Local toxicity appears at the exposure site, such as protein denaturation caused by caustic substances.
In contrast, systemic toxicity requires the toxic agent's absorption and distribution,...
Drug toxicity: Idiosyncratic Reactions01:16

Drug toxicity: Idiosyncratic Reactions

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...
Antiprotozoal Agents01:21

Antiprotozoal Agents

Leishmaniasis is a widespread parasitic disease caused by several Leishmania species. It affects millions of people each year and remains a major public health problem in endemic regions. First-line treatment relies on pentavalent antimonials, including meglumine antimoniate and sodium stibogluconate. Even so, how these drugs work has not been fully clear, especially their interaction with parasite-specific biochemical pathways. One key target is trypanothione reductase (TR), an enzyme that...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Comparative outcomes with low-dose and standard-dose immune checkpoint inhibitors in microsatellite stable advanced gastric/gastroesophageal adenocarcinoma.

ESMO gastrointestinal oncology·2026
Same author

Diroximel fumarate to treat multiple sclerosis.

Drugs of today (Barcelona, Spain : 1998)·2020
Same author

In-Situ Growth of CoS Nanoparticles Onto Electrospun Graphitized Carbon Nanofibers as an Efficient Counter Electrode for Dye-Sensitized Solar Cells.

Journal of nanoscience and nanotechnology·2018
Same author

Improved Visualization of Cortical Lesions in Multiple Sclerosis Using 7T MP2RAGE.

AJNR. American journal of neuroradiology·2018
Same author

Practice Patterns and Outcomes for Pemetrexed Plus Platinum Doublet as Neoadjuvant Chemotherapy in Adenocarcinomas of Lung: Looking Beyond the Usual Paradigm.

Clinical oncology (Royal College of Radiologists (Great Britain))·2017
Same author

Subcorneal Pustular Dermatosis.

Indian journal of dermatology and venereology·2017

Related Experiment Video

Updated: Jun 8, 2026

A Standardized Procedure of Dressing Management for Toxic Epidermal Necrolysis
07:22

A Standardized Procedure of Dressing Management for Toxic Epidermal Necrolysis

Published on: March 14, 2025

Chloroquine-induced toxic epidermal necrolysis.

P Bhargava1, C M Kuldeep, N K Mathur

  • 1Department of Dermatology, SMS Medical College, Jaipur, India.

Indian Journal of Dermatology, Venereology and Leprology
|October 16, 2010
PubMed
Summary

Severe adverse drug reactions, including Stevens-Johnson syndrome and toxic epidermal necrolysis, were observed in two malaria patients following chloroquine phosphate treatment. These cases highlight the critical risks associated with this antimalarial medication.

More Related Videos

Using Terminal Transferase-mediated dUTP Nick End-labelling (TUNEL) and Caspase 3/7 Assays to Measure Epidermal Cell Death in Frogs with Chytridiomycosis
07:37

Using Terminal Transferase-mediated dUTP Nick End-labelling (TUNEL) and Caspase 3/7 Assays to Measure Epidermal Cell Death in Frogs with Chytridiomycosis

Published on: May 16, 2018

Related Experiment Videos

Last Updated: Jun 8, 2026

A Standardized Procedure of Dressing Management for Toxic Epidermal Necrolysis
07:22

A Standardized Procedure of Dressing Management for Toxic Epidermal Necrolysis

Published on: March 14, 2025

Using Terminal Transferase-mediated dUTP Nick End-labelling (TUNEL) and Caspase 3/7 Assays to Measure Epidermal Cell Death in Frogs with Chytridiomycosis
07:37

Using Terminal Transferase-mediated dUTP Nick End-labelling (TUNEL) and Caspase 3/7 Assays to Measure Epidermal Cell Death in Frogs with Chytridiomycosis

Published on: May 16, 2018

Area of Science:

  • Pharmacovigilance
  • Tropical Medicine
  • Dermatology

Background:

  • Malaria remains a significant global health challenge, necessitating effective treatment strategies.
  • Chloroquine phosphate is a widely used antimalarial drug, but its safety profile requires continuous monitoring.
  • Severe cutaneous adverse drug reactions (SCARs) are rare but potentially fatal complications of medication use.

Purpose of the Study:

  • To report two cases of severe adverse drug reactions (Stevens-Johnson syndrome and toxic epidermal necrolysis) in malaria patients treated with chloroquine phosphate.
  • To emphasize the importance of recognizing and managing these rare but life-threatening reactions.
  • To contribute to the understanding of chloroquine-induced dermatological toxicity.

Main Methods:

  • Case report of two female patients diagnosed with malaria.
  • Documentation of treatment regimen, including daily intramuscular injections of chloroquine phosphate for three days.
  • Clinical observation and progression of adverse events, including Stevens-Johnson syndrome and toxic epidermal necrolysis.

Main Results:

  • Both patients presented with symptoms consistent with Stevens-Johnson syndrome after chloroquine phosphate administration.
  • The condition rapidly progressed to toxic epidermal necrolysis in both cases.
  • Despite intensive medical care, both patients unfortunately succumbed to the severe drug reactions.

Conclusions:

  • Chloroquine phosphate, particularly when administered intramuscularly, can be associated with severe and potentially fatal cutaneous adverse drug reactions.
  • Early recognition and prompt management are crucial for SCARs, although outcomes can be poor.
  • This case series underscores the need for vigilance regarding chloroquine's safety, especially in vulnerable populations or when administered via specific routes.