Drug Interactions between Digitek and vibegron
This report displays the potential drug interactions for the following 2 drugs:
- Digitek (digoxin)
- vibegron
Interactions between your drugs
digoxin vibegron
Applies to: Digitek (digoxin) and vibegron
MONITOR: Coadministration with vibegron may increase the serum concentrations of digoxin. The exact mechanism for this interaction has not been established. However, since both agents are substrates for the P-glycoprotein efflux transporter, competitive inhibition is possible. In study subjects, vibegron increased mean digoxin peak serum concentration (Cmax) by 21% and systemic exposure (AUC) by 11%.
MANAGEMENT: Serum digoxin levels should be obtained prior to initiating therapy with vibegron. Monitor pharmacologic response and serum digoxin levels during therapy and after discontinuation of vibegron. Adjust digoxin dosage as needed to attain desired clinical effect.
References (1)
- (2021) "Product Information. Gemtesa (vibegron)." Urovant Sciences, Inc
Drug and food interactions
digoxin food
Applies to: Digitek (digoxin)
Administration of digoxin with a high-fiber meal has been shown to decrease its bioavailability by almost 20%. Fiber can sequester up to 45% of the drug when given orally. Patients should be advised to maintain a regular diet without significant fluctuation in fiber intake while digoxin is being titrated.
Grapefruit juice may modestly increase the plasma concentrations of digoxin. The mechanism is increased absorption of digoxin due to mild inhibition of intestinal P-glycoprotein by certain compounds present in grapefruits. In 12 healthy volunteers, administration of grapefruit juice with and 30 minutes before, as well as 3.5, 7.5, and 11.5 hours after a single digoxin dose (0.5 mg) increased the mean area under the plasma concentration-time curve (AUC) of digoxin by just 9% compared to administration with water. Moreover, P-glycoprotein genetic polymorphism does not appear to influence the magnitude of the effects of grapefruit juice on digoxin. Thus, the interaction is unlikely to be of clinical significance.
References (2)
- Darcy PF (1995) "Nutrient-drug interactions." Adverse Drug React Toxicol Rev, 14, p. 233-54
- Becquemont L, Verstuyft C, Kerb R, et al. (2001) "Effect of grapefruit juice on digoxin pharmacokinetics in humans." Clin Pharmacol Ther, 70, p. 311-6
Therapeutic duplication warnings
No 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.
See also
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. |
Further information
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