Interaction Guide · Research summary

Can I take Radix Et Rhizoma Valerianae with Eszopiclone?

Review Radix Et Rhizoma Valerianae with Eszopiclone: possible adverse effects and timing and monitoring, preparation details, evidence limits, and sources.

Prepared by Dr. Edward M.Kim, PharmD · Clinical Director, SupplementSafety editorial team

Research summary published · Prepared · Editorial update

The short answer

Confirm the valerian species before combining this root product with eszopiclone. If it is Valeriana officinalis, added drowsiness is a reasonable concern; the generic name alone does not establish that identity.

What this answer covers

Generic root/rhizome name does not confirm Valeriana officinalis.

Supplement or preparation
Radix et Rhizoma Valerianae
Medication ingredient
eszopiclone

Eszopiclone’s impairment warning matters

LUNESTA labeling warns of additive CNS depression and next-day impairment, and does not recommend other sedative-hypnotics at bedtime or during the night. This is a co-use precaution, not a measured adverse-event rate for this supplement.

What is known about this product

Valeriana officinalis guidance cautions about combining sedating substances, but the current root name does not identify that species.

Negative findings have a limited scope

The label reports no clinically relevant interaction after single doses with lorazepam, while warning that this does not establish absence of effects during chronic use. Other combinations did impair performance. These findings do not prove either safety or harm for an untested supplement combination.

Plan co-use with the prescriber

Discuss the exact product and other sleep medicines before adding it. A short spacing interval has not been shown to prevent additive impairment. Do not drive while impaired. If sleepwalking, sleep-driving or other activities while not fully awake occur, stop eszopiclone and contact the prescriber promptly, as its label instructs.

Evidence and practical considerations

Side effects & toxicity

Unconfirmed generic valerian identity prevents validation of the original claim with V.officinalis evidence. A separate confirmed-species precaution is retained.

Exact scope
Generic root/rhizome name does not confirm Valeriana officinalis. with Eszopiclone461016 IN; oral LUNESTA tablets, distinct from racemic zopiclone.
Medication form and route
oral medication; oral supplement

What remains uncertain

  • No unmeasured pair incidence, blanket class transfer or arbitrary spacing interval.

Factors that may matter: Preparation; Dose; Other medicines; Organ function.

Research conclusion: insufficient evidence · Evidence assessment: very low

Read the supporting source summaries

Source 1: current product label

dailymed.nlm.nih.gov · Source check Sep 10, 2026

Population: People prescribed eszopiclone

CYP3A4/2E1 metabolism; ketoconazole increased exposure2.2fold. Rifampicin induction evidence measured racemic zopiclone, extrapolated by label. Additive CNS depression and boxed complex sleep behavior warning.

How this applies: Exact eszopiclone RxCUI 461016 IN, with stated salt/formulation/route bridge.

Other-drug results do not establish exact botanical effects; single-dose lorazepam/paroxetine nulls do not predict complete absence of chronic pharmacodynamic effects.

Source 2: federal supplement safety guidance

nccih.nih.gov · Source check Sep 10, 2026

Population: Users of the specified supplement.

Possible but unproven sleep-inducing effects; advises against combining valerian with alcohol or sedatives.

How this applies: Original source interpreted for eszopiclone only within the stated preparation and endpoint limits.

Not a direct eszopiclone combination trial; original preparation, dose and endpoint limits apply. No exact-pair adverse-event rate or protective spacing established.

Source 3: federal botanical identity and safety guidance

ods.od.nih.gov · Source check Sep 10, 2026

Population: Users of Valeriana officinalis.

The fact sheet covers only V. officinalis among more than 250 valerian species; possible additive sedation is theoretical.

How this applies: Original source interpreted for eszopiclone only within the stated preparation and endpoint limits.

Not a direct eszopiclone combination trial; original preparation, dose and endpoint limits apply. No exact-pair adverse-event rate or protective spacing established.

Source 4: original human study

pubmed.ncbi.nlm.nih.gov · Source check Sep 10, 2026

Population: 391 participants with anxiety and insomnia.

Neither botanical improved its primary anxiety/insomnia outcome over placebo.

How this applies: Original source interpreted for eszopiclone only within the stated preparation and endpoint limits.

Four-week kava/valerian insomnia/anxiety efficacy trial; failure to show benefit is not proof of absent sedation. No eszopiclone combination.

Research assessment: · Open full citations ↗

Timing & monitoring

Unconfirmed generic valerian identity prevents validation of the original claim with V.officinalis evidence. A separate confirmed-species precaution is retained.

Exact scope
Generic root/rhizome name does not confirm Valeriana officinalis. with Eszopiclone461016 IN; oral LUNESTA tablets, distinct from racemic zopiclone.
Medication form and route
oral medication; oral supplement

What remains uncertain

  • No unmeasured pair incidence, blanket class transfer or arbitrary spacing interval.

Factors that may matter: Preparation; Dose; Other medicines; Organ function.

Research conclusion: insufficient evidence · Evidence assessment: very low

Read the supporting source summaries

Source 1: current product label

dailymed.nlm.nih.gov · Source check Sep 10, 2026

Population: People prescribed eszopiclone

CYP3A4/2E1 metabolism; ketoconazole increased exposure2.2fold. Rifampicin induction evidence measured racemic zopiclone, extrapolated by label. Additive CNS depression and boxed complex sleep behavior warning.

How this applies: Exact eszopiclone RxCUI 461016 IN, with stated salt/formulation/route bridge.

Other-drug results do not establish exact botanical effects; single-dose lorazepam/paroxetine nulls do not predict complete absence of chronic pharmacodynamic effects.

Source 2: federal supplement safety guidance

nccih.nih.gov · Source check Sep 10, 2026

Population: Users of the specified supplement.

Possible but unproven sleep-inducing effects; advises against combining valerian with alcohol or sedatives.

How this applies: Original source interpreted for eszopiclone only within the stated preparation and endpoint limits.

Not a direct eszopiclone combination trial; original preparation, dose and endpoint limits apply. No exact-pair adverse-event rate or protective spacing established.

Source 3: federal botanical identity and safety guidance

ods.od.nih.gov · Source check Sep 10, 2026

Population: Users of Valeriana officinalis.

The fact sheet covers only V. officinalis among more than 250 valerian species; possible additive sedation is theoretical.

How this applies: Original source interpreted for eszopiclone only within the stated preparation and endpoint limits.

Not a direct eszopiclone combination trial; original preparation, dose and endpoint limits apply. No exact-pair adverse-event rate or protective spacing established.

Source 4: original human study

pubmed.ncbi.nlm.nih.gov · Source check Sep 10, 2026

Population: 391 participants with anxiety and insomnia.

Neither botanical improved its primary anxiety/insomnia outcome over placebo.

How this applies: Original source interpreted for eszopiclone only within the stated preparation and endpoint limits.

Four-week kava/valerian insomnia/anxiety efficacy trial; failure to show benefit is not proof of absent sedation. No eszopiclone combination.

Research assessment: · Open full citations ↗

Side effects & toxicity

If the product is confirmed as Valeriana officinalis, additive drowsiness with eszopiclone is a conditional concern.

Exact scope
Confirmed Valeriana officinalis root product. with Eszopiclone461016 IN; oral LUNESTA tablets, not racemic zopiclone.
Medication form and route
oral medication; oral supplement

What remains uncertain

  • Generic identity remains unresolved; no exact-pair rate or protective spacing.

Factors that may matter: Species; Dose; Other sedatives.

Research conclusion: supported with conditions · Evidence assessment: low

Read the supporting source summaries

Source 1: current product label

dailymed.nlm.nih.gov · Source check Sep 10, 2026

Population: People prescribed eszopiclone

CYP3A4/2E1 metabolism; ketoconazole increased exposure2.2fold. Rifampicin induction evidence measured racemic zopiclone, extrapolated by label. Additive CNS depression and boxed complex sleep behavior warning.

How this applies: Exact eszopiclone RxCUI 461016 IN, with stated salt/formulation/route bridge.

Other-drug results do not establish exact botanical effects; single-dose lorazepam/paroxetine nulls do not predict complete absence of chronic pharmacodynamic effects.

Source 2: federal supplement safety guidance

nccih.nih.gov · Source check Sep 10, 2026

Population: Users of the specified supplement.

Possible but unproven sleep-inducing effects; advises against combining valerian with alcohol or sedatives.

How this applies: Original source interpreted for eszopiclone only within the stated preparation and endpoint limits.

Not a direct eszopiclone combination trial; original preparation, dose and endpoint limits apply. No exact-pair adverse-event rate or protective spacing established.

Source 3: federal botanical identity and safety guidance

ods.od.nih.gov · Source check Sep 10, 2026

Population: Users of Valeriana officinalis.

The fact sheet covers only V. officinalis among more than 250 valerian species; possible additive sedation is theoretical.

How this applies: Original source interpreted for eszopiclone only within the stated preparation and endpoint limits.

Not a direct eszopiclone combination trial; original preparation, dose and endpoint limits apply. No exact-pair adverse-event rate or protective spacing established.

Source 4: original human study

pubmed.ncbi.nlm.nih.gov · Source check Sep 10, 2026

Population: 391 participants with anxiety and insomnia.

Neither botanical improved its primary anxiety/insomnia outcome over placebo.

How this applies: Original source interpreted for eszopiclone only within the stated preparation and endpoint limits.

Four-week kava/valerian insomnia/anxiety efficacy trial; failure to show benefit is not proof of absent sedation. No eszopiclone combination.

Research assessment: · Open full citations ↗

Review and change history

Publication status
Published research summary
Clinical review
Not yet recorded
DateUpdate
Research summary published
Article prepared
Prepared exact eszopiclone article with formulation-specific evidence and uncertainty.

Article revision: 65d045c631eec8b7

This guide brings together the evidence records used by our interaction checker. Each finding retains its own preparation limits, research date, and source summaries.

Full citations require verification. Reading this answer and the source summaries does not.

Taking other supplements or medications?

Use the checker to explore your other combinations. Ask a pharmacist to review the exact products, amounts and medical conditions in your complete list.

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Information, not medical advice. Do not change prescribed treatment based on this guide.