Managing Drug Interactions in the Treatment of HIV-Related Tuberculosis
Table 2a. Recommendations for coadministering antiretroviral drugs with rifampin in adults – 2013
Non-nucleoside reverse transcriptase inhibitors
|
Recommended change in dose of antiretroviral drug |
Recommended change in dose of rifampin |
Comments |
|
Efavirenz
|
None; |
No change |
Effect on efavirenz AUC is highly variable. Efavirenz should not be used during the 1st trimester of pregnancy. |
|
Nevirapine |
Initiate at a dose of 200 mg twice daily rather than 200 mg once daily (use the same maintenance dose of 200 mg twice daily) |
No change |
Efavirenz is preferred, but if nevirapine must be used, lead-in dosing at 200 mg once-daily should be avoided, as this may increase risk of virologic failure. Because of this risk, monitoring of adherence and viral load is recommended. If available, consider therapeutic drug monitoring. |
|
Rilpivirine |
Rifampin and rilpivirine should not be used together |
Rilpivirine AUC ¯ by 80%, Cmin decreased 89% |
||
Etravirine |
Etravirine and rifampin should not be used together |
Marked decrease in etravirine predicted, based on data on the interaction with rifabutin |
Single protease inhibitors
|
Recommended change in dose of antiretroviral drug |
Recommended change in dose of rifampin |
Comments |
|
Atazanavir |
Rifampin and atazanavir should not be used together |
Atazanavir AUC ¯ by >95%. Increasing the dose to 300 mg twice daily or 400 mg twice daily still resulted in subtherapeutic atazanavir concentrations. |
Ritonavir-boosted protease inhibitors
|
Recommended change in dose of antiretroviral drug |
Recommended change in dose of rifampin |
Comments |
|
Lopinavir / ritonavir (Kaletra™) |
Lopinavir 800 mg plus ritonavir 200 mg twice daily (double dose) |
No change |
Use with caution; this combination resulted in hepatotoxicity in all adult healthy volunteers in an initial study. It was better-tolerated among adult patients already taking lopinavir/ritonavir based ART with increase to 600 mg/150 mg after one week, then 800 mg/200 mg one week later. |
|
“Super-boosted” lopinavir / ritonavir |
Lopinavir 400 mg plus ritonavir 400 mg twice daily (super boosting) |
No change |
Use with caution; this combination resulted in hepatotoxicity among adult healthy volunteers. It has not been adequately tested in patients with HIV. |
|
Atazanavir / ritonavir |
Rifampin and atazanavir/ritonavir should not be used together. |
Atazanavir trough concentration ¯ by > 90%. Doubling the dose to 300/100 twice daily resulted in hepatotoxicity in healthy volunteers. |
||
Darunavir / ritonavir |
Rifampin and darunavir/ritonavir should not be used together |
No drug interaction studies of darunavir and rifampin have been conducted. |
||
Fosamprenavir/ritonavir |
Rifampin and fosamprenavir/ritonavir should not be used together |
Fosamprenavir Cmax decreased by 70%, AUC decreased 82%, trough decreased 92% |
||
Saquinavir / ritonavir |
Rifampin and saquinavir/ritonavir should not be used together. |
The combination of saquinavir (1000 mg twice-daily), ritonavir (100 mg twice-daily), and rifampin caused unacceptable rates of hepatotoxicity among healthy volunteers. In tuberculosis patients, 400/400 twice daily caused similar rates of hepatotoxicity. |
CCR-5 receptor antagonists
|
Recommended change in dose of antiretroviral drug |
Recommended change in dose of rifampin |
Comments |
|
Maraviroc |
Increase maraviroc to 600 mg twice-daily |
No change |
The reductions in maraviroc concentrations related to rifampin co-administration may be overcome by increasing the dose, though the 600 mg twice-daily dose has not been formally tested. Use with caution, as there is no reported clinical experience with increased dose of maraviroc with rifampin |
Integrase inhibitors
|
Recommended change in dose of antiretroviral drug |
Recommended change in dose of rifampin |
Comments |
|
Raltegravir |
Increase dose to 800 mg twice daily |
No change |
Raltegravir trough concentrations reduced by 53% even with increased dose to 800 mg twice daily despite reasonable overall exposures. The clinical significance of this is unknown. Use this dose with caution and employ viral load monitoring, if available. |
|
Elvitegravir co-formulated with cobicistat, tenofovir, and emtricitabine (Stribild™) |
Stribild and rifampin should not be used together |
Marked decrease in elvitegravir and cobicistat concentrations predicted based on metabolic pathways of these drugs |
- Page last reviewed: September 24, 2012
- Page last updated: December 9, 2013
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