# Cannabinoid Drug Interactions: Clinical Evidence Review

> **Author:** Benjamin Caplan, MD (ABFM Board Certified, MA Lic. #240562, NPI: 1962722637)
> **Publisher:** CED Clinic (https://cedclinic.com)
> **Canonical URL:** https://cedclinic.com/cannabinoid-drug-interactions/
> **Published:** 2026-04-25T14:02:03-04:00 | **Last Modified / Clinically Audited:** 2026-09-28T10:57:46-04:00
> **Clinical Summary:** Explore clinical evidence on cannabinoid drug interactions, focusing on safety and effects with medications metabolized by cytochrome P450 enzymes.

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#### Clinical Takeaway

CBD commonly inhibits cytochrome P450 enzymes at high doses, potentially increasing levels of medications metabolized through CYP3A4, CYP2C19, and CYP2C9, though clinical significance varies by individual patient factors and CBD dosing. In cancer patients on multiple medications, monitoring for altered drug efficacy or toxicity is warranted when combining CBD with certain opioids, anticoagulants, and antiarrhythmics. Current evidence suggests dose-dependent interactions are possible but serious adverse events remain uncommon in controlled clinical settings.

### #19 Drug Interactions in People on Cannabidiol: Is There Cause for Concern?

**Citation:** Downs Georgia et al. *[Drug Interactions](https://cedclinic.com/cannabis-liver-interactions-study-insights/) in People on Cannabidiol: Is There Cause for Concern?* Cannabis and [cannabinoid research](https://cedclinic.com/cannabinoids-in-reward-processing-pain-perception/). 2026. PMID: 39539239.

**Study type:** Journal Article, Randomized Controlled Trial  | 

**Topic area:** Cannabidiol  | 

**CED Score:** 10

Design: 5 Journal: 1 N: 0 Recency: 3 Pop: 2 Human: 1 Risk: -2

**Quality Gate Alerts:**
- Preclinical only

**Abstract:** INTRODUCTION: Cannabidiol (CBD) exhibits multiple therapeutic properties, but its use in advanced cancer patients raises concerns about potential drug-drug interactions (DDIs) due to polypharmacy. This study aims to look for evidence of DDIs between concomitant medications and CBD oil in a randomized placebo-controlled trial of CBD oil for symptom control (MedCan-1 parent study). MATERIALS AND METHODS: Surrogate measures were used to identify possible drug interactions: (1) the maximum mL of oil self-selected by patients in CBD or placebo groups in relation to opioids, specific drug groups, or individual agents; (2) the occurrence of any new or worse adverse effect in relation to the study arm and the concomitant medication classes/medications of interest. RESULTS: The dose of CBD self-selected by participants was not related to opioid use or medications, including benzodiazepines and antipsychotics. The likelihood of developing an adverse effect while on study or when taking specific medications was not increased by CBD. Participants on paracetamol tolerated a higher dose of CBD. DISCUSSION: Concerns regarding the development of clinically significant drug interactions when taking CBD in the context of anti-cancer and other concomitant medications at least in the short term may be unfounded.

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[View on PubMed ↗](https://pubmed.ncbi.nlm.nih.gov/39539239/)[DOI ↗](https://doi.org/10.1089/can.2024.0041)

 
 
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### Verification & Medical Governance

- **Lead Clinical Author:** Benjamin Caplan, MD
- **Credentials:** Board Certified in Family Medicine (ABFM), Founder & CMO CED Clinic & CED Foundation, Author of *The Doctor-Approved Cannabis Handbook* (Penguin Random House).
- **Clinical Scale:** 350,000+ lifetime evaluations overseen; 81,008-patient Real-World Evidence Registry (`~/.ced_rwe_vault.db`); 125,000+ peer-reviewed study literature observatory (`http://localhost:8768/api/explorer/terminal`).
- **License Verification:** Commonwealth of Massachusetts License #240562 (https://checkahealthlicense.mass.gov/).
- **NPI Registry:** 1962722637 (https://npiregistry.cms.hhs.gov/provider-view/1962722637).
- **Ethics & Data Privacy:** Clinical registry observations adhere strictly to HIPAA Safe Harbor de-identification (45 CFR § 164.514(b)) and criteria for secondary research exemption under 45 CFR § 46.104(d)(4).
