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Zopiclone is a prescription-only sleeping tablet from the group of Z-drugs and is used for short-term, pronounced sleep problems. It reliably shortens the time it takes to fall asleep, but because of the risk of tolerance and dependence the SmPC intends it for a few weeks only. A bitter, metallic taste in the morning is typical — harmless, but the commonest reason why people want to come off the medicine again.
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| Property | Details |
|---|---|
| Active ingredient | Zopiclone |
| ATC code | N05CF01 |
| Drug class | Z-drug (a cyclopyrrolone), a non-benzodiazepine hypnotic |
| Dosage forms | Film-coated tablets of 3.75 mg and 7.5 mg |
| Half-life | Around 5 hours; markedly longer in older people and where liver function is impaired |
| Maximum daily dose | 7.5 mg according to the SmPC; in older people and where there are kidney or liver problems usually 3.75 mg |
| Onset of effect | As a rule within about 30 minutes |
| Prescription status | Prescription-only medicine |
| Notable feature | A bitter, metallic taste as the most typical side effect; according to the SmPC use it for as short a time as possible — a maximum of 4 weeks including the tapering phase |
Zopiclone belongs to the so-called Z-drugs — sleeping tablets whose substance names begin with "Z" and which are chemically not benzodiazepines but act on the same system. It strengthens the action of GABA, the brain's most important inhibitory messenger, by docking onto a particular site on the GABA-A receptor — the same binding site that benzodiazepines such as lorazepam use.¹ The result: the excitability of the nerve cells falls, you become tired and fall asleep faster.
The strengths and the problems of the substance follow equally from this mechanism:
Important for context: zopiclone treats the symptom, not the cause. Why you sleep badly — stress, pain, medicines, a sleep disorder (insomnia) as a condition in its own right — stays unanswered for as long as only the sleeping tablet is running.
The figures below describe what is in the SmPC. They are not a dosing instruction — whether and for how long zopiclone makes sense for you is decided by the treating practice.
Behind this restraint lies a simple principle that doctors have fixed in their minds as a rule of thumb: a clear indication, the smallest effective dose, the shortest possible use, no abrupt stopping and no extension without a fresh assessment. Zopiclone is meant as a bridge through an acute crisis — not as a permanent solution for chronically poor sleep.
With zopiclone the timing decides whether the medicine helps or mainly ruins the next morning.
Your record shows in black and white when the 4-week limit is coming closer.
Zopiclone counts as well tolerated in the short term — the problems that matter arise from the residual effect in the morning and from how long it is used.
Zopiclone impairs reaction time and attention — not only during the night but also the next morning. After a late dose, after the 7.5 mg dose in sensitive people or in combination with other sedating agents, driving the following day is risky and can count in law as driving under the influence of medicines. In the first few days of treatment particular care applies, until you know how you react. In detail in the guide medications and driving.
Zopiclone causes dependence — not in everyone, not after three nights, but reliably enough that the SmPC limits its use to a few weeks. The risk rises with dose and duration and is particularly high in people who have had a dependence disorder before.¹
The mechanism is the same as with the benzodiazepines and can be described in three stages:
You may know the pattern from a quite different substance: with a decongestant nasal spray, continuous use means the nose no longer clears at all without the spray — the remedy creates the problem it is meant to solve. The guide nasal spray dependence describes this vicious circle; with sleeping tablets it runs by the same logic, only with more at stake.
Important for context: taking a low dose over the long term is not a weakness of character but a known, well-described consequence of how the substance works. Nor is it a reason for an abrupt stop — but for a planned, supported exit (section 8).
The critical interactions of zopiclone almost all follow one principle: anything that sedates on top of it or slows its breakdown increases the carry-over, the memory gaps and the depression of breathing.
| Combination | Consequence | What to do |
|---|---|---|
| Alcohol | Unpredictably increased sedation, memory gaps, falls, complex sleep behaviours | Avoid it completely during the treatment |
| Benzodiazepines (e.g. lorazepam) and other Z-drugs such as zolpidem | The same mechanism twice over — an overdose effect, a raised risk of dependence | Do not combine; any switch only with medical support |
| Opioid painkillers | Increased depression of breathing and sedation | Combine only where a doctor has expressly prescribed it that way |
| Sedating antidepressants and antihistamines | Additive tiredness, a hangover lasting into the day | Have your overall medication checked at the practice or the pharmacy |
| CYP3A4 inhibitors (e.g. erythromycin, clarithromycin, ketoconazole) | Zopiclone is broken down more slowly, effect and side effects are increased | Inform your practice; a dose adjustment may be needed |
| CYP3A4 inducers (e.g. rifampicin, St John's wort) | Faster breakdown, a weakened effect | Always mention herbal preparations too |
The point that matters most in practice: many sedating agents are available over the counter — antihistamines "for travel sickness", herbal calming preparations, cold remedies with a sedating component. Taken together they make a cocktail that nobody would have prescribed that way. Check combinations in the guide to drug interactions or directly in the interaction check in the brite app.
The commonest mistake on the way out is stopping cold after taking it for a longer time — and the commonest trap is called rebound insomnia: after stopping, you sleep worse for a few nights than you did before the treatment. The brain, which has got used to the damping, overshoots in the opposite direction. Anyone who does not know about this reads it as proof ("so I do need the medicine after all") and starts again — and the circle closes.
What helps during the rebound nights: build up sleep pressure (go to bed later rather than earlier), get up at a fixed time in the morning, no naps during the day — and take the nights for what they are: temporary. The general principles for ending a course of medication are explained in the guide stopping medications.
The honest order of priority is set out in the German S3 guideline on insomnia in adults (DGSM, AWMF 063-003): the first choice for chronic sleep problems is cognitive behavioural therapy for insomnia (CBT-I) — not a medicine.²,⁴ It combines sleep restriction, stimulus control and work on night-time rumination, and it works more durably than any sleeping tablet, because it takes apart the anticipatory fear of the sleepless night. Digital CBT-I programmes are available on prescription in Germany.
In terms of medicines, the comparison looks like this:
| Option | Strengths | Limits |
|---|---|---|
| Zopiclone | A reliable aid to falling asleep for a short period | Tolerance and dependence after weeks, bitter taste, hangover |
| Zolpidem | A shorter half-life, so it tends to leave less carry-over | The same mechanism, the same risk of dependence — no way out of the problem |
| Benzodiazepines (e.g. lorazepam) | Also relieve anxiety | A higher potential for dependence, a longer duration of action, more carry-over — for sleep problems alone rarely the first choice |
| Melatonin | No potential for dependence, licensed in the prolonged-release form for older people | Effectiveness rather moderate, helps above all where the sleep rhythm has shifted |
| Sedating antidepressants (e.g. low-dose mirtazapine) | No dependence, useful where there is accompanying depression | Side effects of their own (weight gain, daytime tiredness); used off-label, or only where the diagnosis fits |
Switching from zopiclone to zolpidem — or the other way round — does not, incidentally, solve the underlying problem: both Z-drugs act at the same receptor, and tolerance and dependence simply travel with you. An honest overview of all the options, including sleep hygiene, is given in the guide sleeping pills: what really helps?.
In older age zopiclone is a special case with a clear message: the 7.5 mg dose is on the PRISCUS 2.0 list of medicines regarded as potentially inappropriate for older people in Germany.⁵ The reason: the breakdown slows down, the substance goes on working for longer — and the combination of muscle relaxation, drowsiness and a trip to the toilet at night markedly increases the risk of falls and of a fractured neck of femur. If it is used at all in older age, it is at 3.75 mg and for a very short time. What to bear in mind about medication in older people generally is brought together in the guide medications in old age.
Pregnancy and breastfeeding: zopiclone is not among the medicines of choice. The advisory centre Embryotox judges the data to be limited; taken towards the end of pregnancy it can lead to adaptation problems and poor feeding in the newborn.⁶ If you are pregnant or would like to become pregnant, talk to your practice about alternatives — the guide medications during pregnancy gives you your bearings.
Kidneys and liver: where liver function is impaired, zopiclone is broken down markedly more slowly — the SmPC provides for the lower dose here, and in severe liver failure it is not suitable. In advanced kidney failure the dose is lower as well. The basics on this are in the guide medications for kidney and liver disease.
Respiratory conditions: in severe COPD, untreated sleep apnoea and myasthenia, zopiclone is contraindicated or can be used only with great restraint — the effect on breathing weighs particularly heavily here.
While you are taking the medicine, usually not completely; afterwards, yes. The taste arises because the active substance is excreted in the saliva — so it is not a sign of intolerance but part of normal breakdown. It can be eased by taking the tablet immediately before lying down, by brushing your teeth thoroughly in the morning and with things that mask the taste, such as chewing gum or lemon water. For many people it turns out to be a useful ally: every morning it reminds them that the medicine is not meant to be a permanent arrangement.
Possibly, but that is no reason to panic — and certainly no reason to stop immediately. Typical pointers are: the effect has worn off, you no longer get to sleep at all without a tablet, the thought of a night without one makes you uneasy. The right way is an open conversation with your practice and a tapering plan worked out together. Abrupt withdrawal after months is unpleasant to risky and is usually the reason why attempts to come off it fail.
Intermittent treatment agreed with your doctor can make sense, because it reduces the total dose and the habituation. Improvised on your own, though, it has its pitfalls: if you experience the "free" nights as a battle and the tablet as a reward, you are more likely to train the psychological dependence. What counts is a fixed plan — nights decided in advance instead of a spontaneous decision at 1 in the morning.
A lower dose does indeed reduce the residual effect — which is why 3.75 mg is the strength provided for sensitive people and for older people. Whether half the dose still works well enough for you, and whether your tablets can be divided at all, is something to settle with your practice or your pharmacy. More important than the question of dose is often the timing: the later you take it, the more certain the hangover.
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