Drug Interactions between amprenavir and cat's claw
This report displays the potential drug interactions for the following 2 drugs:
- amprenavir
- cat's claw
Interactions between your drugs
amprenavir cat's claw
Applies to: amprenavir and cat's claw
GENERALLY AVOID: A case report suggests that concomitant use of cat's claw may increase the plasma concentrations of protease inhibitors. The exact mechanism of interaction is unknown, although cat's claw has been found in one study to inhibit CYP450 3A4 metabolism in vitro. The case patient was a 45-year-old woman with HIV and hepatitis C coinfection who was scheduled to receive a liver transplantation. Her antiretroviral regimen prior to transplantation consisted of abacavir (600 mg/day), lamivudine (300 mg/day), atazanavir (300 mg/day), ritonavir (100 mg/day), and saquinavir (2000 mg/day). In addition, she was receiving sildenafil and epoprostenol for pulmonary hypertension. When serum protease inhibitor levels were measured before the transplantation, trough levels (Cmin) were 1.22 mcg/mL for atazanavir, 6.13 mcg/mL for ritonavir, and 3.4 mcg/mL for saquinavir. No signs or symptoms of overdosage were observed. Subsequent questioning of the patient revealed that she had been taking a cat's claw preparation for the past two months, which was the only relevant change according to the authors. The patient was instructed to discontinue the herbal product. Two weeks later, Cmin values normalized to 0.3 mcg/mL for atazanavir, 0.92 mcg/mL for ritonavir, and 0.64 mcg/mL for saquinavir. The patient continued on the same antiretroviral regimen thereafter without further incident.
MANAGEMENT: Although data are limited, use of cat's claw preparations should preferably be avoided in patients treated with protease inhibitors. Otherwise, clinicians should consider monitoring serum protease inhibitor levels, especially following initiation or discontinuation of any cat's claw product. Patients should consult a healthcare provider before taking any herbal or alternative medicine.
References (2)
- Budzinski JW, Foster BC, Vandenhoek S, Arnason JT (2000) "An in vitro evaluation of human cytochrome P450 3A4 inhibition by selected commercial herbal extracts and tinctures." Phytomedicine, 7, p. 273-82
- Lopez Galera RM, Ribera Pascuet E, Esteban Mur JI, Montoro Ronsano JB, Juarez Gimenez JC (2008) "Interaction between cat's claw and protease inhibitors atazanavir, ritonavir and saquinavir." Eur J Clin Pharmacol
Drug and food interactions
amprenavir food
Applies to: 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
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