Drug Interactions between cat's claw and ritonavir
This report displays the potential drug interactions for the following 2 drugs:
- cat's claw
- ritonavir
Interactions between your drugs
ritonavir cat's claw
Applies to: ritonavir 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
ritonavir food
Applies to: ritonavir
ADJUST DOSING INTERVAL: Administration with food may modestly affect the bioavailability of ritonavir from the various available formulations. When the oral solution was given under nonfasting conditions, peak ritonavir concentrations decreased 23% and the extent of absorption decreased 7% relative to fasting conditions. Dilution of the oral solution (within one hour of dosing) with 240 mL of chocolate milk or a nutritional supplement (Advera or Ensure) did not significantly affect the extent and rate of ritonavir absorption. When a single 100 mg dose of the tablet was administered with a high-fat meal (907 kcal; 52% fat, 15% protein, 33% carbohydrates), approximately 20% decreases in mean peak concentration (Cmax) and systemic exposure (AUC) were observed relative to administration after fasting. Similar decreases in Cmax and AUC were reported when the tablet was administered with a moderate-fat meal. In contrast, the extent of absorption of ritonavir from the soft gelatin capsule formulation was 13% higher when administered with a meal (615 KCal; 14.5% fat, 9% protein, and 76% carbohydrate) relative to fasting.
MANAGEMENT: Ritonavir should be taken with meals to enhance gastrointestinal tolerability.
References (1)
- (2001) "Product Information. Norvir (ritonavir)." Abbott Pharmaceutical
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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