Drug Interactions between nelfinavir and Rescriptor
This report displays the potential drug interactions for the following 2 drugs:
- nelfinavir
- Rescriptor (delavirdine)
Interactions between your drugs
nelfinavir delavirdine
Applies to: nelfinavir and Rescriptor (delavirdine)
MONITOR: Coadministration with delavirdine may significantly increase the plasma concentrations of nelfinavir. The mechanism is delavirdine inhibition of nelfinavir metabolism via CYP450 3A4 and 2C19. According to the delavirdine labeling, coadministration of delavirdine (400 mg three times a day) and nelfinavir (750 mg three times a day) for 7 days increased the mean peak plasma concentration (Cmax), area under the concentration-time curve (AUC) and trough plasma concentration (Cmin) of nelfinavir by 88%, 107% and 136%, respectively, compared to administration of nelfinavir alone. Plasma concentrations of the active metabolite, nelfinavir hydroxy-t-butylamide, were significantly reduced but were more than compensated for by the increased nelfinavir concentration. Delavirdine Cmax, AUC and Cmin decreased by 27%, 31% and 33%, respectively.
MANAGEMENT: Appropriate dosages for the combination of nelfinavir and delavirdine with respect to safety and efficacy have not been established. Patients should be monitored for toxicity such as elevations in liver function tests, neutropenia, and undue gastrointestinal disturbances, especially diarrhea.
References (2)
- (2001) "Product Information. Rescriptor (delavirdine)." Pharmacia and Upjohn
- Developed by the panel of Clinical Practices for Treatment of HIV Infection convened by the Department of Health and Human Services (DHHS) (2004) Guidelines for the use of antiretroviral agents in HIV-1-infected adults and adolescents. http://AIDSinfo.nih.gov
Drug and food interactions
No alcohol/food interactions were found. However, this does not necessarily mean no interactions exist. Always consult your healthcare provider.
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
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
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