Drug Interactions between cat's claw and fosamprenavir
This report displays the potential drug interactions for the following 2 drugs:
- cat's claw
- fosamprenavir
Interactions between your drugs
cat's claw fosamprenavir
Applies to: cat's claw and fosamprenavir
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
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
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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