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What is Zopivane (Zopiclone) and How Is It Used?

3 min read

Affecting up to 30% of the population, insomnia is a common sleep disorder for which medications may be prescribed. What is zopivane? Zopivane is a brand name for zopiclone, a non-benzodiazepine hypnotic agent, or 'Z-drug', used for the short-term relief of severe insomnia.

Quick Summary

Zopiclone, sold under brand names like Zopivane, is a prescription sedative-hypnotic for short-term insomnia. It works by calming the brain to help with falling and staying asleep but carries risks of dependence and side effects.

Key Points

  • What it is: Zopivane is a brand name for zopiclone, a sedative-hypnotic 'Z-drug' for short-term treatment of severe insomnia.

  • How it works: It enhances the effect of GABA, a calming chemical in the brain, to induce sleep and reduce nighttime awakenings.

  • Usage: A healthcare professional will determine the appropriate dose, often lower for the elderly or those with liver/kidney issues.

  • Short-Term Use Only: Treatment is typically limited to 2-4 weeks to avoid tolerance and dependence.

  • Common Side Effects: The most frequent side effects are a metallic taste in the mouth, daytime drowsiness, and dry mouth.

  • Major Risks: Risks include dependence, withdrawal symptoms upon stopping, and complex sleep behaviors like sleepwalking.

  • US Availability: Zopiclone is not sold in the US, but its active component, eszopiclone (Lunesta), is approved and available by prescription.

In This Article

Understanding Zopiclone: A Closer Look

Zopiclone, available under brand names including Zopivane, Imovane, and Zimovane, is a prescription sedative-hypnotic medication. It belongs to a class of drugs known as cyclopyrrolones and is often referred to as a "Z-drug," along with zolpidem and zaleplon. While structurally different from benzodiazepines, zopiclone functions similarly by enhancing the effects of a natural calming chemical in the brain called gamma-aminobutyric acid (GABA). This action slows down brain activity, helping to induce sleep. It is primarily prescribed for the short-term treatment of severe insomnia, helping patients fall asleep more quickly, stay asleep longer, and reduce nighttime awakenings. Due to the risk of tolerance and dependence, its use is typically recommended for short periods, ranging from a few days to a maximum of four weeks. Zopiclone is not commercially available in the United States; however, its active stereoisomer, eszopiclone (brand name Lunesta), is.

Proper Usage

Proper administration of zopiclone is critical for safety and efficacy. A healthcare professional will determine the appropriate dose. A lower starting dose may be recommended for individuals over 65 or those with kidney or liver problems to minimize risks like next-day drowsiness. It is crucial to take the tablet whole, without crushing or chewing it, and only when you can ensure a full 7 to 8 hours of uninterrupted sleep. Taking zopiclone without allowing for a full night's sleep increases the risk of side effects like memory impairment (amnesia) and next-day grogginess. Alcohol should be strictly avoided while taking zopiclone, as it can dangerously amplify the sedative effects, leading to excessive sedation and respiratory depression.

Potential Side Effects and Risks

The most common side effect associated with zopiclone is a bitter or metallic taste in the mouth. Other common effects include drowsiness, dry mouth, dizziness, and headache. While generally mild, zopiclone can also cause more serious side effects. These include memory loss (amnesia), hallucinations, depression, and complex sleep-related behaviors like sleepwalking, sleep-driving, or making phone calls while not fully awake. The risk of falls, particularly in the elderly, is also a significant concern.

Dependence, Withdrawal, and Long-Term Use

One of the most significant risks associated with zopiclone is the potential for dependence and addiction, especially with long-term use or at doses higher than prescribed. The body can develop a tolerance, requiring higher doses to achieve the same effect. Abruptly stopping the medication after prolonged use can lead to withdrawal symptoms, including rebound insomnia, anxiety, shaking, heart palpitations, and, in rare cases, seizures. For this reason, treatment is typically limited to four weeks, and discontinuation should be done gradually under a doctor's supervision. Studies on chronic users have suggested that long-term use may not provide better sleep than that of drug-free individuals with insomnia and may be associated with higher levels of anxiety and depression.

Z-Drugs Comparison: Zopiclone vs. Eszopiclone vs. Zolpidem

Zopiclone, eszopiclone, and zolpidem are all "Z-drugs" used to treat insomnia, but they have distinct differences.

Feature Zopiclone Eszopiclone (Lunesta) Zolpidem (Ambien)
Primary Use Short-term insomnia (difficulty falling/staying asleep) Insomnia (approved for longer-term use in the US) Primarily for difficulty falling asleep
Half-Life ~5-6 hours ~6 hours Shorter half-life (~2.5-4.5 hours)
Key Difference Racemic mixture; not available in the US. The active S-isomer of zopiclone; available in the US. Acts quickly but for a shorter duration.
Common Side Effect Metallic taste, drowsiness Unpleasant taste, headache Drowsiness, dizziness

Eszopiclone is the active component of zopiclone and is thought to be responsible for most of its hypnotic effects. While zolpidem is better for sleep initiation due to its rapid onset and shorter duration, zopiclone and eszopiclone are often used for sleep maintenance because they last longer.

Conclusion

Zopivane (zopiclone) is an effective medication for the short-term management of severe insomnia, helping users fall asleep and stay asleep. However, its use must be carefully managed by a healthcare professional due to significant risks, including a distinctive metallic taste, next-day impairment, and, most importantly, the potential for tolerance, dependence, and withdrawal. Treatment should be limited to the shortest possible duration at the lowest effective dose. Non-pharmacological alternatives, such as Cognitive Behavioral Therapy for Insomnia (CBT-I), have been found to be superior for long-term management and should be considered.


For more information on zopiclone, please visit the NHS page on Zopiclone.

Frequently Asked Questions

No, zopiclone is a non-benzodiazepine hypnotic from the cyclopyrrolone class. However, it acts on the brain in a similar way to benzodiazepines by modulating GABA receptors.

Zopiclone works quickly, typically taking about one hour to take effect.

No, you should not drink alcohol while taking zopiclone. Alcohol can increase the sedative effects, making you sleep too deeply and potentially causing breathing problems or difficulty waking up.

The most frequently reported side effect of zopiclone is a bitter or metallic taste in the mouth.

Zopiclone is prescribed for short-term use (typically 2-4 weeks) because the body can quickly develop tolerance, meaning it becomes less effective. There is also a significant risk of physical and psychological dependence with longer use.

Stopping zopiclone abruptly after long-term use can cause withdrawal effects, including rebound insomnia, anxiety, irritability, sweating, and headaches. A doctor will typically recommend reducing the dose gradually.

No, zopiclone (Zopivane) is not commercially available in the US. However, eszopiclone (brand name Lunesta), which is the active isomer of zopiclone, is approved and available by prescription.

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.