Drug Interaction Report
1 potential interaction and/or warning found for the following 2 drugs:
- Lentocilin (penicillin g benzathine)
- seladelpar
Interactions between your drugs
penicillin G benzathine seladelpar
Applies to: Lentocilin (penicillin g benzathine), seladelpar
GENERALLY AVOID: Concomitant administration with inhibitors of the organic anion transporter 3 (OAT3) may increase the plasma concentrations of seladelpar, which is a substrate of this renal transporter. Administration of the OAT3 inhibitor probenecid (500 mg four times daily) to healthy subjects on days 1 through 4, with a single dose of seladelpar (10 mg) administered on day 2 resulted in an increase of seladelpar's systemic exposure (AUC) and maximum plasma concentration (Cmax) of 2- and 4.69-fold, respectively. Additionally, the mean cumulative urinary excretion of seladelpar was unquantifiable in the presence of probenecid, compared to 2.1 mcg in the absence of probenecid.
MANAGEMENT: Concurrent use of seladelpar with OAT3 inhibitors should generally be avoided.
References (2)
- (2024) "Product Information. Livdelzi (seladelpar)." Gilead Sciences
- Cymabay Therapeutics Inc (2024) Center for drug evaluation and research. Application Number: 217899Orig1s000 integrated review. https://www.accessdata.fda.gov/drugsatfda_docs/nda/2024/217899Orig1s000IntegratedR.pdf
Drug and food interactions
No alcohol/food interactions were found with the drugs in your list. However, this does not necessarily mean no food interactions exist. Always consult your healthcare provider.
Therapeutic duplication warnings
No duplication warnings were found for your selected drugs.
Therapeutic duplication warnings are only returned when drugs within the same group exceed the recommended therapeutic duplication maximum.
Drug Interaction Classification
Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit. | |
Moderately clinically significant. Usually avoid combinations; use it only under special circumstances. | |
Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan. | |
No interaction information available. |
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Further information
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