Drug Interaction Report
1 potential interaction and/or warning found for the following 2 drugs:
- riluzole
- Tabrecta (capmatinib)
Interactions between your drugs
riluzole capmatinib
Applies to: riluzole, Tabrecta (capmatinib)
GENERALLY AVOID: Coadministration with capmatinib may increase the plasma concentrations and risk of adverse effects of drugs that are substrates of CYP450 1A2. The proposed mechanism is decreased clearance due to capmatinib-mediated inhibition of CYP450 1A2 isoenzyme. Coadministration with capmatinib increased the systemic exposure (AUC0-INF) of caffeine (a CYP450 1A2 substrate) by 134%, but did not affect the peak plasma concentration (Cmax) of caffeine.
MANAGEMENT: Coadministration of capmatinib with drugs that are substrates of CYP450 1A2 should generally be avoided. However, if concomitant use is unavoidable, caution is advised, particularly with drugs that have a narrow therapeutic range. Clinical and laboratory monitoring should be considered whenever capmatinib is added to or withdrawn from therapy with these drugs, and the dosages adjusted as necessary. Patients should be monitored for the development of adverse effects.
References (1)
- (2020) "Product Information. Tabrecta (capmatinib)." Novartis Pharmaceuticals
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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