2-(3-methoxyphenyl)-2-(ethylamino)cyclohexanone and Seizures

2-(3-methoxyphenyl)-2-(ethylamino)cyclohexanone has been researched along with Seizures* in 3 studies

Other Studies

3 other study(ies) available for 2-(3-methoxyphenyl)-2-(ethylamino)cyclohexanone and Seizures

ArticleYear
[Methoxetamine-associated emergencies. First Spanish descriptions of this new drug].
    Medicina clinica, 2015, Nov-06, Volume: 145, Issue:9

    Topics: Akathisia, Drug-Induced; Alcohol Drinking; Cocaine; Cyclohexanones; Cyclohexylamines; Drug Overdose; Emergencies; Female; Humans; Illicit Drugs; Male; Rape; Seizures; Spain; Young Adult

2015
Analytical findings of an acute intoxication after inhalation of methoxetamine.
    Journal of analytical toxicology, 2014, Volume: 38, Issue:7

    Methoxetamine (MXE) is increasingly used and abused, as it is frequently presented as being safer than ketamine, and legal. Cases of only MXE consumption being associated with the occurrence of seizures are rarely reported. A single MXE intoxication case by inhalation is described concerning a 21-year-old man, not known to be epileptic, who was found collapsed in his bedroom, supposedly after an epileptic seizure. He was transferred to the Emergency Department of the Henri Mondor Hospital, Aurillac, France. He was conscious, but with a sinus bradycardia (48/min) and an ST-segment elevation on the electrocardiogram, and a slightly increased creatine kinase level (270 U/L) and hyponatremia (127 mmol/L). New seizure activity occurred during hospitalization, but the clinical course in the intensive care unit was favorable. Quantitation of MXE in serum and urine using gas chromatography coupled to mass spectrometry (GC-MS) was developed, as well as a liquid chromatography coupled to tandem mass spectrometry (LC-MS-MS) method for the determination of MXE in hair. Limits of detection and quantification were, respectively, 2 and 10 µg/L for the GC-MS method and both 0.5 pg/mg for the LC-MS-MS method. Concentrations of 30 and 408 µg/L were, respectively, measured in serum and urine. Concentrations of 135 and 145 pg/mg were detected in two 2.5 cm hair strands, consistent with one or several consumptions during the 2 ½ months prior to sampling. A sample of the powder consumed was available and also analyzed. This case illustrates the dangers of this drug, which justify its classification as a narcotic in France since August 2013.

    Topics: Cyclohexanones; Cyclohexylamines; Gas Chromatography-Mass Spectrometry; Hair; Humans; Illicit Drugs; Inhalation Exposure; Limit of Detection; Male; Reproducibility of Results; Seizures; Spectrometry, Mass, Electrospray Ionization; Substance Abuse Detection; Young Adult

2014
Acute methoxetamine and amphetamine poisoning with fatal outcome: a case report.
    International journal of occupational medicine and environmental health, 2014, Volume: 27, Issue:4

    Methoxetamine (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.

    Topics: Acute Disease; Adult; Amphetamine; Cyclohexanones; Cyclohexylamines; Fatal Outcome; Humans; Illicit Drugs; Male; Seizures

2014