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Ronlax
Overdose can cause sleepiness, agitation, and impaired coordination, with symptoms occurring more frequently and severely in children. Fatal asphyxia attributed to benzodiazepine toxicity has been reported in three elderly patients taking therapeutic maintenance doses for two to three weeks.1 High doses of fluvoxamine may intensify its adverse effects.
Dosage & Duration
Dosage
Doses are population estimates that vary widely between individuals.
Duration
Subjective Effects
Pharmacology
Pharmacodynamics
Ronlax (ethyl loflazepate) acts through a mechanism similar to that of other benzodiazepines. Most of its pharmacological activity is attributed to an active metabolite that is more potent than the parent compound.
Pharmacokinetics
Ethyl loflazepate was developed as a prodrug and is converted into an active metabolite.2 Its elimination half-life is 51-103 hours. Kidney impairment or failure does not affect the accumulation of its active metabolites.
Interactions
An unlisted combination is an unknown one, not a safe one. Check a dedicated combination chart before mixing.
Tolerance
Harm Potential
Addiction & Dependence
Psychological
HighEthyl loflazepate/Ronlax is classified as a depressant and habit-forming.
Toxicity
Animal studies found low toxicity, but deaths from therapeutic maintenance doses over 2 to 3 weeks were reported in three elderly patients, attributed to asphyxia due to benzodiazepine toxicity. Overdose symptoms include sleepiness, agitation, ataxia, and severe hypotonia.
Reported deaths in elderly patients were attributed to asphyxia due to benzodiazepine toxicity.
Overdose symptoms include sleepiness, agitation, ataxia, and severe hypotonia.
Long-term very high doses in rats produced pulmonary phospholipidosis with pulmonary foam cells.
History & Culture
Legality
References
Citations
Article Status
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