Zopiclone
Zopiclone is a non-benzodiazipine hypnotic. Zopiclone is used for short term treatment of insomnia (sleeping disorders).
Primary Characteristics
It is of Synthetic origin and belongs to Cyclopyrolones.
It belongs to Chloride Channel Potentiater (GABA operated) pharmacological group on the basis of mechanism of action. It is also classified under Psychotherapeutic Drugs .
Molecular Weight: 388.8 · pKa: 6.7 · Solubility in Water: Insoluble · Solubility in Alcohol: Insoluble · Non-proprietary name: Zopiclone.

Pharmacokinetics
Absorption: Zopiclone has an oral bioavailability is 96.5% (±1.5%).
Distribution: Zopiclone has a volume of distribution is 100 litre. plasma protein binding is 45 %.
Elimination: plasma half-life is 3.5 - 6 hr, renal excretion is 4 - 5 %.
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Indications
Zopiclone is primarily indicated in conditions like Insomnia, Nausea, vertigo, labyrinthine disorders.
Contraindications
Zopiclone is contraindicated in conditions like Respiratory insufficiency.
Dosage
Zopiclone's dosage details are as follows:
| Dose | Single Dose | Frequency | Route | Instructions |
|---|---|---|---|---|
| Adult Dosage | ||||
| 0.17 mg/kg | 0.17 mg/kg | Every 24h | PO | - |
| Paediatric Dosage (20kg) | ||||
| 0 – 0 | — | — | Not recommended in this age group | |
| Neonatal Dosage (3kg) | ||||
| 0 – 0 | — | — | Not recommended in this age group | |
Drug Interactions
Always consult your physician for the change of dose regimen or an alternative drug of choice that may strictly be required.
Side Effects
The signs and symptoms that are produced after acute overdosage of Zopiclone are Drowsiness, Ataxia, Lethargy.
Zopiclone is known to cause more or less tolerable side effects which are usually transient. These include Confusion, Depressive moods, Irritability.
Warnings / Precautions
Available Brands
None recorded.
Storage Conditions
Drug Classification
- 1.24.3 — Drugs used in anxiety and sleep disorders