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Acute methoxetamine and amphetamine poisoning with fatal outcome: A case report

Marek Wiergowski, Jacek Anand, Maciej Krzyżanowski, Zbigniew Jankowski

International Journal of Occupational Medicine and Environmental Health January 1, 2014 DOI: 10.2478/s13382-014-0290-8 (opens in new tab)

Summary

AI-generated from the abstract

A 31-year-old man died after taking methoxetamine (MXE) and amphetamine recreationally. He arrived at the hospital in a deep coma with respiratory failure, hyperthermia, seizures, and signs of organ damage. Despite intensive care, he died four weeks later from multi-organ failure. Blood tests showed MXE at a toxic level (0.32 μg/ml) and amphetamine at a non-toxic level (0.06 μg/ml). Amphetamine was also found in his hair, suggesting prior use. The combination likely caused a severe, adverse interaction.

Study at a glance

Characteristics Case study Case report Peer reviewed
Sample size 1
Population A 31-year-old man
Key finding Recreational use of methoxetamine and amphetamine resulted in fatal multi-organ failure, with MXE present at toxic concentrations.

Abstract

AbstractMethoxetamine (MXE) is a psychoactive substance distributed mostly via the Internet and is not liable to legal regulation in Poland. MXE has a toxicity profile similar to that of ketamine but longer-lasting effects. The paper describes a case of acute poisoning that resulted from recreational use of MXE and amphetamine and ended in death. In mid-July 2012, a 31-year old man was admitted to the clinical toxicology unit in Gdańsk because of poisoning with an unknown psychoactive substance. The patient was transported to the emergency department (ED) at 5:15 a.m. in a very poor general condition, in a deep coma, with acute respiratory failure, hyperthermia (> 39°C) and generalized seizures. Laboratory tests showed marked leukocytosis, signs of massive rhabdomyolysis, hepatic failure and beginning of acute renal failure. Despite intensive therapy, the patient died 4 weeks after the poisoning in the course of multi-organ dysfunction syndrome. Chemical and toxicological studies of serum and urine samples collected on the poisoning day at 1:40 p.m. confirmed that amphetamine and MXE had been taken earlier that day. Concentration of amphetamine in the serum (0.06 μg/ml) was within the non-toxic range, while MXE (0.32 μg/ml) was within the toxic range of concentrations. Amphetamine was also detected in the patient’s hair, which suggested a possibility of its use within the last dozen weeks or so. The serious clinical course of intoxication and co-existence of amphetamine and MXE in the patient’s blood and urine suggest the possibility of adverse interactions between them.

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