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Zopiclone, Zaleplon and Zolpidem

Group: Depressants
Nicknames: Z-drugs, Ambien, Stilnox, Imovane, Zimovane, Sonata, eszopiclone, Lunesta, zimmos, zees
Last reviewed: October 2026

Pharmacology

Zolpidem exerts its effects through targeting the same GABA-A receptor binding site as benzodiazepines (for more information, see Diazepam). Unlike benzodiazepines however, it shows marked selectivity for GABA-A receptors containing the alpha-1 subunit, leading to its effects being more hypnotic than anxiolytic or anti-convulsant.

Z-drugs in immediate release formulations have an onset time of 30–60 min, while slow release can increase this up to 3 hours. Zopiclone has the longest duration of the Z-drugs (half-life ≈ 5–7 hours, half life of zolpidem ≈ 2 hours and Zaleplon ≈ 1 hour), leading to more residual effects similar to short acting benzos.

Zopiclone and zolpidem are primarily broken down by the CYP3A4 enzyme, so it is recommended to avoid taking them in conjunction with CYP3A4 inhibitors (e.g. clarithromycin, erythromycin, diltiazem, itraconazole, ketoconazole, ritonavir, verapamil, and grapefruit juice), as they may increase unwanted side effects and risk of overdose.

As Z-drugs have a similar mechanism of action to benzos, taking them alongside opioids, alcohol, GHB/GBL, and/or gabapentinoids significantly increases the risk of overdose.

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