Zopiclone is supplied by Lime Pharmacy following an online medical assessment. A valid prescription is required before dispensing.
| Drug Name: | Zopiclone / Zop |
| Dosage: | 7.5 mg / 10 mg |
| Packages: | 30 – 180 pills |
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Zopiclone is a prescription-only medication widely used for the short-term treatment of insomnia and other sleep disorders. It belongs to a group of medicines known as non-benzodiazepine hypnotics, or cyclopyrrolone derivatives, commonly referred to as “Z-drugs.” Although chemically different from benzodiazepines, zopiclone acts on similar brain receptors to promote sleep.
This article provides an educational overview of zopiclone, covering how it works, approved medical uses, dosing guidance, potential side effects, safety precautions, interactions, dependence risks, and regulatory considerations.
Zopiclone is a short-term hypnotic medicine used to help people fall asleep and stay asleep. It was introduced in the 1980s as an alternative to traditional benzodiazepines, with the aim of reducing next-day sedation and lowering the risk of long-term dependence when used appropriately.
From a chemical standpoint, zopiclone belongs to the cyclopyrrolone class. It is typically supplied as immediate-release tablets in strengths such as 3.75 mg, 5 mg, or 7.5 mg. In many countries, including the UK, zopiclone is classified as a controlled prescription-only medicine because of its potential for misuse and dependence.
Zopiclone works by enhancing the effects of gamma-aminobutyric acid (GABA), the main inhibitory neurotransmitter in the brain. It binds to the GABA-A receptor complex at a site similar to benzodiazepines, increasing the flow of chloride ions into nerve cells. This results in:
Compared with traditional benzodiazepines, zopiclone has a relatively short half-life of around five hours, which helps limit residual sedation the following morning when taken correctly.
The primary indication for zopiclone is the short-term management of insomnia. It may be prescribed for people experiencing:
To reduce the risk of tolerance and dependence, treatment is generally limited to a maximum of two to four weeks.
Zopiclone may also be used temporarily for short-lived sleep problems related to stress, travel, shift work, or significant life events. In these cases, it is typically used as a short bridging treatment while underlying causes are addressed.
In some cases, zopiclone may be prescribed short term for individuals with depression, anxiety, or other psychiatric conditions who are experiencing acute sleep disruption. It is used only as an adjunct and not as a primary treatment for these disorders.
Zopiclone is intended for short-term use only. Prolonged or continuous use increases the risk of dependence, tolerance, and withdrawal symptoms.
Most people tolerate zopiclone well when used short term at recommended doses. Side effects are usually mild and temporary.
Because zopiclone acts on the central nervous system, careful use under medical supervision is essential.
Zopiclone can interact with other medicines that depress the central nervous system, increasing sedation and overdose risk.
Zopiclone is metabolised by the CYP3A4 enzyme. Medicines that inhibit this enzyme may increase zopiclone levels, while enzyme inducers may reduce its effectiveness.
Although initially considered lower risk than benzodiazepines, zopiclone can cause both physical and psychological dependence when used for extended periods or at higher doses.
To minimise withdrawal effects, healthcare providers usually recommend gradual dose reduction rather than abrupt discontinuation.
Zopiclone is a prescription-only medicine in most countries.
| Drug | Class | Half-life | Notes |
|---|---|---|---|
| Zopiclone | Z-drug | 5 hrs | Effective for sleep onset and maintenance |
| Eszopiclone | Z-drug | 6 hrs | Active isomer of zopiclone |
| Zolpidem | Z-drug | 2–3 hrs | Shorter duration of action |
| Temazepam | Benzodiazepine | 8–10 hrs | Higher dependence risk |
For long-term management of insomnia, non-drug approaches are often recommended:
Zopiclone can be an effective short-term option for managing severe insomnia when used according to medical guidance. However, its potential for side effects, dependence, and withdrawal means it should be prescribed cautiously and reviewed regularly.
For ongoing sleep problems, combining short-term medication use with behavioural and lifestyle-based treatments offers a safer and more sustainable approach.
Zopiclone is used for the short-term treatment of insomnia, helping people fall asleep faster and reduce night-time awakenings.
Zopiclone can be habit-forming if used for longer than recommended or at higher doses. Medical supervision is important.
Most guidelines recommend limiting use to two to four weeks to reduce dependence and withdrawal risks.
No. Zopiclone is a prescription-only medicine due to its safety profile and misuse potential.
Zopiclone usually starts to take effect within 30 to 60 minutes after ingestion. It should be taken immediately before going to bed, once you are ready to sleep.
The sedative effects typically last between 6 and 8 hours. Zopiclone has a half-life of around 5 hours, which helps reduce next-day drowsiness when taken at the correct dose.
Zopiclone can be prescribed to older adults, but at lower doses, usually 3.75 mg. Older people are more sensitive to sedative effects and have a higher risk of falls, confusion, and prolonged sedation.
Using zopiclone beyond the recommended duration increases the risk of tolerance, dependence, and withdrawal symptoms. Long-term use may also reduce its effectiveness for sleep.
No. Zopiclone is intended only for short-term use. For long-term or chronic insomnia, non-drug treatments such as cognitive behavioural therapy for insomnia (CBT-I) are generally recommended.
Combining zopiclone with other sedatives, sleep aids, or alcohol is not recommended, as this can significantly increase the risk of excessive sedation, breathing problems, and overdose.