Drug Interactions between Agenerase and efavirenz
This report displays the potential drug interactions for the following 2 drugs:
- Agenerase (amprenavir)
- efavirenz
Interactions between your drugs
efavirenz amprenavir
Applies to: efavirenz and Agenerase (amprenavir)
ADJUST DOSE: Coadministration with efavirenz may decrease the plasma concentrations of amprenavir. The mechanism is efavirenz induction of CYP450 3A4, the isoenzyme responsible for the metabolic clearance of amprenavir. In one study, median plasma amprenavir trough level (Cmin) was 25% of the expected mean following 14 days of coadministration of amprenavir (1200 mg twice a day) and efavirenz (600 mg once a day) in seven HIV-infected patients. Overall, six of the seven patients had subtherapeutic amprenavir levels, and three had amprenavir Cmin values that were below 20% of the expected mean by as early as day 7. The addition of ritonavir (100 mg twice a day) to reduced dosages of amprenavir (450 to 900 mg twice a day) in the six patients resulted in increased amprenavir trough levels by 15- to 90-fold. In another study, efavirenz decreased the mean steady-state peak plasma concentration (Cmax), systemic exposure (AUC) and Cmin of amprenavir by 33%, 24% and 43%, respectively, in nine antiretroviral-experienced HIV patients treated with amprenavir, abacavir, and various nucleoside reverse transcriptase inhibitors. Amprenavir did not affect the pharmacokinetics of efavirenz.
MANAGEMENT: The dosage of amprenavir or its prodrug, fosamprenavir, should probably be increased when coadministered with efavirenz in the absence of ritonavir as a pharmacokinetic booster, although appropriate dosages with respect to safety and efficacy have not been established. Fosamprenavir labeling recommends an additional 100 mg/day (300 mg total) of ritonavir when efavirenz is administered with the fosamprenavir-ritonavir once-daily regimen based on pharmacokinetic studies. No change in the ritonavir dose is required when efavirenz is administered with the fosamprenavir-ritonavir twice-daily regimen.
References (5)
- (2001) "Product Information. Agenerase (amprenavir)." Glaxo Wellcome
- Falloon J, Piscitelli S, Vogel S, Sadler B, Mitsuya H, Kavlick MF, Yoshimura K, Rogers M, LaFon S, Manion DJ, Lane HC, Masur (2000) "Combination therapy with amprenavir, abacavir, and efavirenz in human immunodeficiency virus (HIV)-infected patients failing a protease-inhibitor regimen: Pharmacokinetic drug interactions and antiviral activity." Clin Infect Dis, 30, p. 313-8
- Wintergerst U, Engelhorn C, Kurowski M, Hoffmann F, Notheis G, Belohradsky BH (2000) "Pharmacokinetic interaction of amprenavir in combination with efavirenz or delavirdine in HIV-infected children." Aids, 14, p. 1866-8
- (2003) "Product Information. Lexiva (fosamprenavir)." GlaxoSmithKline
- Duval X, Le Moing V, Longuet P, et al. (2000) "Efavirenz-induced decrease in plasma amprenavir levels in human immunodeficiency virus-infected patients and correction by ritonavir." Antimicrob Agents Chemother, 44, p. 2593
Drug and food interactions
efavirenz food
Applies to: efavirenz
ADJUST DOSING INTERVAL: Administration with food increases the plasma concentrations of efavirenz and may increase the frequency of adverse reactions. According to the product labeling, administration of efavirenz capsules (600 mg single dose) with a high-fat/high-caloric meal (894 kcal, 54 g fat, 54% calories from fat) or a reduced-fat/normal-caloric meal (440 kcal, 2 g fat, 4% calories from fat) was associated with mean increases of 39% and 51% in efavirenz peak plasma concentration (Cmax) and 22% and 17% in systemic exposure (AUC), respectively, compared to administration under fasted conditions. For efavirenz tablets, administration of a single 600 mg dose with a high-fat/high-caloric meal (approximately 1000 kcal, 500-600 kcal from fat) resulted in a 79% increase in mean Cmax and a 28% increase in mean AUC of efavirenz relative to administration under fasted conditions.
GENERALLY AVOID: Alcohol may potentiate the central nervous system (CNS) depressant effects of efavirenz. Concomitant use may result in additive CNS depression and impairment of judgment, thinking, and psychomotor skills. In more severe cases, hypotension, respiratory depression, profound sedation, coma, or even death may occur.
MANAGEMENT: Efavirenz should be taken on an empty stomach, preferably at bedtime. Dosing at bedtime may improve the tolerability of nervous system symptoms such as dizziness, insomnia, impaired concentration, somnolence, abnormal dreams and hallucinations, although they often resolve on their own after the first 2 to 4 weeks of therapy . Patients should be advised of the potential for additive central nervous system effects when efavirenz is used concomitantly with alcohol or psychoactive drugs, and to avoid driving or operating hazardous machinery until they know how the medication affects them.
References (4)
- (2001) "Product Information. Sustiva (efavirenz)." DuPont Pharmaceuticals
- (2023) "Product Information. Sustiva (efavirenz)." Bristol-Myers Squibb, SUPPL-59/47
- (2024) "Product Information. Stocrin (efavirenz)." Merck Sharp & Dohme (Australia) Pty Ltd
- (2024) "Product Information. Efavirenz (efavirenz)." Viatris UK Healthcare Ltd
amprenavir food
Applies to: Agenerase (amprenavir)
GENERALLY AVOID: Administration with a high-fat meal may decrease the oral bioavailability of amprenavir. The mechanism is unknown. In healthy volunteers, consumption of a standardized high-fat meal decreased the peak plasma concentration (Cmax) and area under the concentration-time curve (AUC) of amprenavir (1200 mg single oral dose) by 36% and 21%, respectively, compared to administration in the fasted state. The time to reach Cmax (Tmax) was increased 44% following a high-fat meal.
Grapefruit juice does not appear to significantly affect the pharmacokinetics of amprenavir. In 12 healthy volunteers, administration with grapefruit juice (200 mL) decreased the mean peak plasma concentration (Cmax) of amprenavir (1200 mg single oral dose) by 22% compared to water. The median time to reach Cmax (Tmax) was prolonged from 0.75 to 1.13 hours. These pharmacokinetic changes are not thought to be clinically significant, since antiretroviral response is more closely associated with systemic exposure (AUC) and trough plasma concentration (Cmin), which were not affected in the study.
MANAGEMENT: Amprenavir may be taken with or without food, but should not be taken with a high-fat meal.
References (2)
- (2001) "Product Information. Agenerase (amprenavir)." Glaxo Wellcome
- Demarles D, Gillotin C, Bonaventure-Paci S, Vincent I, Fosse S, Taburet AM (2002) "Single-dose pharmacokinetics of amprenavir coadministered with grapefruit juice." Antimicrob Agents Chemother, 46, p. 1589-1590
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.
Check Interactions
To view an interaction report containing 4 (or more) medications, please sign in or create an account.
Save Interactions List
Sign in to your account to save this drug interaction list.