Lurasidone

For an informed discussion with your doctor or pharmacist. This information collection is not a clinically validated interaction checker. Missing data do not establish safety. Do not change or stop prescribed medicines on the basis of this information. The findings apply to the specific conditions studied; laboratory and animal studies cannot be directly extrapolated to humans.

Active substance: Lurasidone

Examples of brand names: Latuda [EU/USA]

ATC code: N05AE05

Main use (for orientation): Schizophrenia

Documented research summary

Psychosis-treatment cases, some involving synthetic substances, are not controlled cannabinoid-interaction experiments.

Uncertainties and limitations

Does not establish safety for less-studied cannabinoids or untested formulations/doses.

Do not infer clinical dosage from preclinical effects or enzyme hypotheses.

Research is limited to the specified date and protocol; it is not globally exhaustive. Brand names and authorisations do not constitute a complete current market overview.

Structured assessment

Category: Drug context

Cannabinoid scope: 28 register names in the documented search family; neither 28 individual clinical trials nor a blanket assessment of all cannabinoids.

Evidence status: Insufficient pair-specific data

Mechanism / drug context: Lurasidone: CYP3A4; food substantially changes exposure.

Type of supporting material: Medicine information and documented individual review; no positive pair trial

Clinical interpretation: Requires individual assessment by a doctor or pharmacist. Lack of evidence does not establish safety; no dosage or discontinuation advice is provided.

Context: Oral lurasidone hydrochloride US Remedyrepack; this generic label lists bipolar depression alone or with lithium/valproate. Do not automatically transfer a schizophrenia indication from another label. Active D2/5-HT2A/5-HT7 antagonist and partial 5-HT1A agonist; not solely a prodrug. Strong CYP3A4 inhibitors/inducers contraindicated in regulatory information.

Drug context and gaps in search results are not measured interactions. The source role below describes which statement the source actually supports.

Source role [C_LABEL_D0126]: Drug context

Statement supported: Supports dosage form, metabolism and/or known risks; alone, it does not substantiate a cannabinoid–drug pair finding.

Source: LURASIDONE HYDROCHLORIDE (LURASIDONE HYDROCHLORIDE) TABLET, FILM COATED [REMEDYREPACK INC.] [C_LABEL_D0126]

Source role [C_PR_36498129]: Scope distinction / context

Statement supported: Psychosis-treatment cases following cannabis use, some involving synthetic cannabinoids; no defined study of the pair.

Source: Lurasidone use in Cannabis-Induced Psychosis: A Novel Therapeutic Strategy and Clinical Considerations in Four Cases Report. [C_PR_36498129]

Scope of review: Individual research with documented title/abstract screening and targeted review of original sections. This is not exhaustive evidence that interactions are absent.

Unresolved source question: The complete stored individual review, label review, literature screening, conclusion and uncertainties were read. Targeted sections of original information were rechecked; no claim is made that all product information or full texts were completely revalidated.

Separately recorded findings

No separately substantiated finding for this drug–cannabinoid pair is recorded within the documented scope of review. This does not prove that no such study exists anywhere or that the combination is safe.

References and access status

[C_LABEL_D0126] LURASIDONE HYDROCHLORIDE (LURASIDONE HYDROCHLORIDE) TABLET, FILM COATED [REMEDYREPACK INC.]

Original source / bibliographic reference

Authors: REMEDYREPACK INC.

Year: 2026

Source type: US Structured Product Label

Source access – 23 October 2026: Source destination was accessible when checked.

Bibliographic attribution or source identity cross-checked.

[C_PR_36498129] Lurasidone use in Cannabis-Induced Psychosis: A Novel Therapeutic Strategy and Clinical Considerations in Four Cases Report.

Original source / bibliographic reference

Authors: Ricci V, Martinotti G, De Berardis D, Maina G.

Year: 2022

Source type: Primary source, full text read

DOI: 10.3390/ijerph192316057

PMID: 36498129

Source access – 23 October 2026: Automated direct retrieval was restricted; this does not establish that the link is broken.

Bibliographic attribution or source identity cross-checked.

PubMed – bibliographic reference / abstract

PubMed Central – archived text

DOI – publisher access (access restrictions may apply)

Research as of 23 October 2026. Not all original full texts could be reviewed in full. Source accessibility and the strength of scientific evidence must be assessed separately. An accessible link does not establish medical approval; a bibliographic record with an abstract does not replace the original full text.

Drug search and explanation of the evidence · Guide: cannabinoids and medicines · Author and responsibility