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Rifabutin and Saquinavir

Determining the interaction of Rifabutin and Saquinavir and the possibility of their joint administration.

Check result:
Rifabutin <> Saquinavir
Relevance: 14.11.2022 Reviewer: Shkutko P.M., M.D., in

In the database of official manuals used in the service creation an interaction registered by statistical results of studies was found, which can either lead to negative consequences for the patient health or strengthen a mutual positive effect. A doctor should be consulted to address the issue of joint drug administration.

Consumer:

Using rifabutin together with saquinavir may decrease the effects of saquinavir. Contact your doctor if your condition changes. If your doctor does prescribe these medications together, you may need a dose adjustment or special test to safely use both medications. It is important to tell your doctor about all other medications you use, including vitamins and herbs. Do not stop using any medications without first talking to your doctor.

Professional:

ADJUST DOSE: Coadministration with rifabutin may decrease the plasma concentrations of saquinavir. The mechanism is rifabutin induction of saquinavir metabolism via CYP450 3A4. According to the product labeling, coadministration of saquinavir mesylate (hard gelatin capsule, or HGC, 600 mg three times a day) with rifabutin (300 mg once a day) for 14 days resulted in a 30% decrease in steady-state saquinavir peak plasma concentration (Cmax) and a 43% decrease in systemic exposure (AUC) in a group of 12 HIV-infected subjects. Similarly, in a study of 14 HIV-infected patients, rifabutin (300 mg once a day for 10 days) decreased the mean steady-state Cmax and AUC of saquinavir (soft gelatin capsule, or SGC, 1200 mg three times a day for 10 days) by 39% and 47%, respectively, compared to administration of saquinavir alone. Steady-state rifabutin Cmax and AUC increased by an average of approximately 45% each. In another study, coadministration of saquinavir mesylate/ritonavir (HGC 400 mg/400 mg twice a day) with rifabutin (150 mg every 3 days or 300 mg every 7 days) in 24 patients resulted in a 39% increase in saquinavir Cmax and a 19% increase in AUC, which are not considered clinically significant. In addition, when compared to a rifabutin 150 mg once daily dose, administration of rifabutin 150 mg every four days with saquinavir mesylate/ritonavir (1000 mg/100 mg twice a day) in 11 healthy volunteers did not affect the systemic exposure over 96 hours (AUC (0-96)) of rifabutin but increased the Cmax by 68%; however, the AUC (0-96) and Cmax of the rifabutin active moiety (sum of rifabutin and 25-O-desacetyl rifabutin) by 60% and 111%, respectively. The saquinavir and ritonavir levels were not significantly affected.

MANAGEMENT: No dose adjustment of saquinavir/ritonavir (1000 mg/100 mg twice a day) is recommended if used in combination with rifabutin. However, it is recommended that the dose of rifabutin be reduced to 150 mg every other day or three times per week. Patients receiving the combination should also be monitored for liver enzyme elevations and other potential signs and symptoms of rifabutin toxicity such as leukopenia, uveitis, arthralgia, and skin discoloration. Plasma concentration monitoring of rifabutin may be considered. Rifabutin should not be used with saquinavir mesylate in the absence of ritonavir as a pharmacokinetic booster. In addition, unboosted saquinavir is not indicated as the sole protease inhibitor in the treatment of HIV-infected adults; it should only be given with low-dose ritonavir in combination with other antiretroviral agents. In general, treatment of tuberculosis (TB) and Mycobacterium avium-intracellulare complex in the context of antiretroviral therapy is complex and requires an individualized approach. Experts in the treatment of these conditions should be consulted.

References
  • "Product Information. Invirase (saquinavir)." Roche Laboratories, Nutley, NJ.
  • Cerner Multum, Inc. "UK Summary of Product Characteristics." O 0
  • "Notice to readers: updated guidelines for the use of rifabutin or rifampin for the treatment and prevention of tuberculosis among HIV-infected patients taking protease inhibitors or nonnucleoside reverse transcriptase inhibiotrs." MMWR Morb Mortal Wkly Rep 49 (2000): 185-9
  • American Thoracic Society, CDC, Infectious Diseases Society of America "Treatment of tuberculosis." MMWR Morb Mortal Wkly Rep 52(RR-11) (2003): 1-77
  • Durant J, Clevenbergh P, Garraffo R, Halfon P, Icard S, DelGiudice P, Montagne N, Schapiro JM, Dellamonica P "Importance of protease inhibitor plasma levels in HIV-infected patients treated with genotypic-guided therapy: pharmacological data from the Viradapt Study." Aids 14 (2000): 1333-9
  • Cerner Multum, Inc. "Australian Product Information." O 0
  • Burman WJ, Jones BE "Treatment of HIV-related tuberculosis in the era of effective antiretroviral therapy." Am J Respir Crit Care Med 164 (2001): 7-12
  • Moyle GJ, Buss NE, Goggin T, Snell P, Higgs C, Hawkins DA "Interaction between saquinavir soft-gel and rifabutin in patients infected with HIV." Br J Clin Pharmacol 54 (2002): 178-82
Rifabutin

Generic Name: rifabutin

Brand name: Mycobutin

Synonyms: n.a.

Saquinavir

Generic Name: saquinavir

Brand name: Invirase, Fortovase

Synonyms: n.a.

In the course of checking the drug compatibility and interactions, data from the following reference sources was used: Drugs.com, Rxlist.com, Webmd.com, Medscape.com.

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