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Drug Interactions between fosamprenavir and raltegravir

This report displays the potential drug interactions for the following 2 drugs:

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Interactions between your drugs

Moderate

fosamprenavir raltegravir

Applies to: fosamprenavir and raltegravir

MONITOR: Coadministration of fosamprenavir (with or without ritonavir) and raltegravir may decrease the plasma concentrations of both amprenavir and raltegravir. The mechanism of interaction has not been described. In 14 study subjects, administration of fosamprenavir 1400 mg twice a day (under fasting conditions) in combination with raltegravir 400 mg twice a day for 14 days decreased the amprenavir peak plasma concentration (Cmax), systemic exposure (AUC) and trough plasma concentration (Cmin) by 27%, 36% and 43%, respectively. When the same dosages were given without regards to food, amprenavir Cmax, AUC and Cmin decreased by 15%, 17% and 32%, respectively. In 14 study subjects, administration of fosamprenavir 700 mg plus ritonavir 100 mg twice a day (under fasting conditions) in combination with raltegravir 400 mg twice a day for 14 days decreased the amprenavir Cmax, AUC and Cmin by 14%, 17% and 20%, respectively. When the same dosages were given without regards to food, amprenavir Cmax, AUC and Cmin decreased by 15%, 17% and 32%, respectively. In 13 study subjects, administration of fosamprenavir 1400 plus ritonavir 100 mg once a day (under fasting conditions) in combination with raltegravir 400 mg twice a day for 14 days decreased the amprenavir Cmax, AUC and Cmin by 18%, 24% and 50%, respectively. When the same dosages were given without regards to food, amprenavir Cmax and AUC increased by 27% and 13%, respectively, but the Cmin decreased by 17%.

MANAGEMENT: Caution is advised if fosamprenavir is prescribed in combination with raltegravir. Appropriate dosages of the combination with respect to safety and efficacy have not been established.

References

  1. (2003) "Product Information. Lexiva (fosamprenavir)." GlaxoSmithKline

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Drug and food interactions

Moderate

fosamprenavir food

Applies to: fosamprenavir

ADJUST DOSING INTERVAL: Food may reduce the systemic bioavailability of amprenavir from fosamprenavir oral suspension. The mechanism of interaction has not been described. According to the product labeling, administration of fosamprenavir oral suspension (1400 mg single dose) with a high-fat meal (967 kcal, 67 g fat, 33 g protein, 58 g carbohydrate) reduced amprenavir peak plasma concentration (Cmax) by 46% and systemic exposure (AUC) by 28% compared to administration in a fasted state. The time to reach peak plasma level (Tmax) was delayed by 0.72 hours. In contrast, the same high-fat meal did not affect the pharmacokinetics of amprenavir from fosamprenavir tablets.

MANAGEMENT: Fosamprenavir suspension should be administered on an empty stomach in adults, but with food in pediatric patients to aid palatability and compliance. If emesis occurs within 30 minutes after dosing the suspension, the dose should be repeated. Fosamprenavir tablets may be taken with or without food.

References

  1. (2003) "Product Information. Lexiva (fosamprenavir)." GlaxoSmithKline

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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.


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Drug Interaction Classification

These classifications are only a guideline. The relevance of a particular drug interaction to a specific individual is difficult to determine. Always consult your healthcare provider before starting or stopping any medication.
Major Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit.
Moderate Moderately clinically significant. Usually avoid combinations; use it only under special circumstances.
Minor 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.
Unknown No interaction information available.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.