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Etizolam (marketed under many trademark name) is a thienodiazepine derivative which is a benzodiazepine analog. The etizolam particle varies from a benzodiazepine in that the benzene ring has actually been replaced by a thiophene ring and triazole ring has actually been fused, making the drug a thienotriazolodiazepine.
Although a thienodiazepine, etizolam is scientifically regarded as a benzodiazepine because of its mode of action by means of the benzodiazepine receptor and straight targeting GABAA receptors.
It has anxiolytic, amnesic, anticonvulsant, hypnotic, sedative and skeletal muscle relaxant properties. Etizolam is an anxiolytic discovered to have lower tolerance and reliance liability than benzodiazepines
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Short-term treatment of sleeping disorders.
Stress and anxiety conditions such as OCD and general anxiety condition, primarily as a short-term medication to be utilized purely on an at-need basis
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Negative effects:
Long term use might lead to blepharospasms, especially in ladies. Dosages of 4 mg or more might trigger anterograde amnesia. In rare cases, erythema annulare centrifugum skin lesions have resulted.
Tolerance, dependence and withdrawal
Abrupt or rapid discontinuation from etizolam, similar to benzodiazepines, might lead to the appearance of the benzodiazepine withdrawal syndrome, including rebound insomnia. Neuroleptic malignant syndrome, an uncommon occasion in benzodiazepine
withdrawal, has actually been documented in a case of abrupt withdrawal from etizolam.
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This is especially appropriate offered etizolam’s brief half-life relative to benzodiazepines such as diazepam resulting in a quicker drug level decline in blood plasma levels.
In a study that compared the effectiveness of etizolam, alprazolam, and bromazepam for the treatment of generalized stress and anxiety disorder, all 3 drugs retained their effectiveness over 2 weeks, but etizolam ended up being more effective from 2 weeks to 4 weeks. Administering.5 mg etizolam twice daily did not cause cognitive deficits over 3 weeks when compared to placebo.
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When numerous doses of etizolam, or lorazepam, were administered to rat neurons, lorazepam triggered downregulation of alpha-1 benzodiazepine binding websites (tolerance/dependence), while etizolam triggered an increase in alpha-2 benzodiazepine binding websites (reverse tolerance to anti-anxiety effects).
Tolerance to the anticonvulsant effects of lorazepam was observed, however no significant tolerance to the anticonvulsant impacts of etizolam was observed. Etizolam for that reason has a decreased liability to cause tolerance, and reliance, compared to timeless benzodiazepines.
Etizolam might represent a possible anxiolytic of option with lowered liability to produce tolerance and reliance after long-lasting treatment of anxiety and stress syndromes.
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Cases of intentional suicide by overdose using etizolam in mix with GABA agonists have actually been reported. Although etizolam has a lower LD50 than particular benzodiazepines, the LD50 is still far beyond the prescribed or suggested dosage.
Flumazenil, a GABA antagonist representative utilized to reverse benzodiazepine overdoses, prevents the impact of etizolam along with classical benzodiazepines such as diazepam and chlordiazepoxide.
Etizolam overdose deaths are increasing for instance, the National Records of Scotland report on drug-related deaths, ‘street’ Etizolam was a factor in (“implicated in, or potentially contributed to”) 752, or 59%, of drug-related deaths in Scotland in 2019.
It is essential to highlight that more than one drug contributed to the huge majority of the deaths (by way of contrast, opiates and opioids were a factor in 1092, or 86%, of drug-related deaths).
