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A Comprehensive Review of MDMA and GHB: Two Common Club Drugs

Christian J. Teter, Sally K. Guthrie

Pharmacotherapy The Journal of Human Pharmacology and Drug Therapy December 1, 2001 DOI: 10.1592/phco.21.20.1486.34472 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Review Peer reviewed
Topics MDMA Serotonin
Keywords Rhabdomyolysis Gamma hydroxybutyrate Serotonin syndrome Coma optics Anesthesia Intensive care medicine Euphoriant Amphetamine Narcolepsy Hallucinogen Modafinil Pharmacology Dopamine
Citations 114
Key findings MDMA and GHB have nonlinear pharmacokinetics, produce distinct toxic syndromes, and require specific supportive treatments.

Abstract

“Club drugs” have become alarmingly popular. The use of 3,4‐methylenedioxymethamphetamine (MDMA, Ecstasy) and γ‐hydroxybutyrate (GHB), in particular, has increased dramatically from 1997–1999. The pharmacokinetics of MDMA and GHB appear to be nonlinear, making it difficult to estimate a dose‐response relationship. The drug MDMA is an amphetamine analog with sympathomimetic properties, whereas GHB is a γ‐aminobutyric acid analog with sedative properties. Symptoms of an MDMA toxic reaction include tachycardia, sweating, and hyperthermia. Occasional severe sequelae include disseminated intravascular coagulation, rhabdomyolysis, and acute renal failure. Treatment includes lowering the body temperature and maintaining adequate hydration. Symptoms of GHB intoxication include coma, respiratory depression, unusual movements, confusion, amnesia, and vomiting. Treatment includes cardiac and respiratory support. Because of the popularity of these agents and their potentially dangerous effects, health care professionals must be familiar with these substances and the treatment options for patients who present with symptoms of a toxic reaction.

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