Dapagliflozin
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: Dapagliflozin
Examples of brand names: Forxiga [EU/DE]
ATC code: A10BK01
Main use (for orientation): Diabetes; heart/renal failure
Documented research summary
Existing finding B0103 confirmed: a physiologically based pharmacokinetic model predicts increased dapagliflozin AUC with an assumed CBD regimen and UGT1A9 fraction. This is not a measured clinical interaction. No second database row created for the same finding.
Uncertainties and limitations
Model-article abstract read; model validation and sensitivity analyses not fully independently reconstructed.
Missing data do not establish safety. Research is limited by the documented sources, search terms, languages and accessibility.
Separately recorded findings
1 separately recorded finding. Each statement applies to its documented study context.
CBD – theoretical plausibility
Finding ID: B0103
Type of result: Context-specific finding; read the limitations
Observation: Predicted AUC increase of 126%.
Mechanism: UGT1A9 inhibition; PBPK
Study type: PBPK model based on in vitro data
Context studied: Model: repeated oral CBD 700 mg twice daily; dapagliflozin fm 0.80.
Clinical interpretation: Clinical relevance unresolved; validation needed
Limitations and uncertainties: Not an observed patient drug–drug interaction; not a dosing recommendation.
Original sources for this finding: Predicting in vivo cannabinoid-drug interactions mediated via inhibition of UDP-glucuronosyltransferases using in vitro studies and physiologically based pharmacokinetic modeling and simulations [ME04]
References and access status
[VD_LABEL_D0254] DAPAGLIFLOZIN TABLET, FILM COATED [ASCEND LABORATORIES, LLC] – DailyMed SPL
Original source / bibliographic reference
Authors: Marketing authorisation holder / label provider according to the linked DailyMed product information
Year: 2026
Source type: Regulatory product information (US SPL)
Source access – 23 October 2026: Source destination was accessible when checked.
Bibliographic attribution or source identity cross-checked.
[ME04] Predicting in vivo cannabinoid-drug interactions mediated via inhibition of UDP-glucuronosyltransferases using in vitro studies and physiologically based pharmacokinetic modeling and simulations
Original source / bibliographic reference
Authors: Bansal S; Paine MF; Unadkat JD
Year: 2025
Source type: Original study: in vitro UGT and PBPK
DOI: 10.1016/j.dmd.2025.100096
PMID: 40482431
Source access – 23 October 2026: Source destination was accessible when checked.
Bibliographic attribution or source identity cross-checked.
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
Dapagliflozin and cannabinoids: documented findings, evidence, sources and data gaps. Research information for discussion with your doctor or pharmacist.
