Zopiclone For Anxiety

Zopiclone For Anxiety, Zopiclone, sold under the brand name Imovane among others, is a nonbenzodiazepine used to treat difficulty sleeping. Zopiclone is molecularly distinct from benzodiazepine drugs and is classed as a cyclopyrrolone.

Zopiclone is indicated for the short-term treatment of insomnia in adults. The approved adult dose is 7.5 mg taken shortly before bedtime for up to a maximum of 4 weeks. Medsafe has not assessed the safety and efficacy of longer-term use.

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Zopiclone should be administered with caution in patients exhibiting symptoms of depression. Suicidal tendencies may be present in depressive patients therefore the least amount of zopiclone that is feasible should be supplied to these patients to avoid the possibility of intentional overdosage by the patient. Pre-existing depression may be unmasked during use of zopiclone. Since insomnia may be a symptom of depression, the patient should be re-evaluated if insomnia persists.

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Zopiclone takes around 1 hour to work.

You might feel sleepy or confused in the first few days after taking zopiclone.

Do not drive a car, ride a bike, or use tools or machines until you know how zopiclone affects your ability to do these activities.

Talk to your GP or pharmacist if you are unsure if it is safe for you to drive while taking zopiclone.

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Like other sedative/hypnotic drugs, zopiclone has CNS-depressant effects. The risk of psychomotor impairment, including impaired driving ability, is increased if: zopiclone is taken within 12 hours of performing activities that require mental alertness, a dose higher than the recommended dose is taken, or zopiclone is co-administered with other CNS depressants, alcohol or with other drugs that increase the blood levels of zopiclone (see section 4.5).

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Zopiclone is eliminated via hepatic metabolism, therefore, hepatic impairment increases the risk of adverse effects. In healthy adults, the elimination half-life of zopiclone after a single dose is 5 hours. In patients with hepatic failure, the elimination half-life is prolonged to nearly 12 hours

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Complex sleep behaviour, including sleep walking and other associated behaviours such as “sleep driving”, preparing and eating food, or making phone calls or having sex, with amnesia for the event, have been reported in patients who have taken zopiclone and were not fully awake. The use of alcohol and other CNS-depressants with zopiclone appears to increase the risk of such behaviours, as does the use of zopiclone at doses exceeding the maximum recommended dose. These events may occur following the first or any subsequent use of zopiclone.

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