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. 2013 Winter;24(4):217–238. doi: 10.1155/2013/781410

TABLE 10.

Drug-drug interactions among antiretroviral agents, and telaprevir and boceprevir

Antiretroviral agent Boceprevir Telaprevir
Non-nucleoside reverse transcriptase inhibitors
Efavirenz 44% ↓ Cmin, 19% ↓ AUC of boceprevir (183). Avoid combination (126) 47% ↓ Cmin of telaprevir (214); consider ↑ telaprevir dose to 1125 mg every 8 h with efavirenz (172)
Etravirine 29% ↓ Cmin, 23% ↓ AUC of etravirine. Clinical relevance unclear (175) No clinically significant changes in either drug. No dose adjustment required (173)
Rilpivirine ↑ 39% AUC, ↑ 15% Cmax, ↑ 10% Cmin of rilpivirine, not considered clinically significant. No dose adjustment required (176) ↑ 78% AUC, ↑ 49% Cmax, ↑ 93% Cmin of rilpivirine, not considered clinically significant. No dose adjustment required (173)
Protease inhibitors
Atazanavir/ritonavir 49% ↓ Ctrough, 35% ↓ AUC of atazanavir (170). Avoid combination 85% ↑ Cmin of atazanavir (172). Combination may be used
Darunavir/ritonavir 59% ↓ Ctrough, 44% ↓ AUC of darunavir and 32% ↓ boceprevir (170). Avoid combination 40% ↓ AUC and 42% ↓ Cmin of darunavir, 35% ↓ AUC and 32% ↓ Cmin of telaprevir (172). Avoid combination (169)
Fosamprenavir/ritonavir No data 47% ↓ AUC and 56% ↓ Cmin of amprenavir, 32% ↓ AUC and 30% ↓ Cmin of telaprevir (172). Avoid combination (169)
Lopinavir/ritonavir 43% ↓ Ctrough, 34% ↓ AUC of lopinavir and 45% ↓ boceprevir (170). Avoid combination 6% ↑ AUC and 14% ↑ Cmin of lopinavir, 54% ↓ AUC and 52% ↓ Cmin of telaprevir (172). Avoid combination (169)
Integrase inhibitors
Raltegravir No clinically significant changes in either drug. No dose adjustment required (177) No clinically significant changes in either drug. No dose adjustment required (178)
Reverse transcriptase inhibitors
Tenofovir No clinically significant changes in either drug. No dose adjustment required (183) No clinically significant changes in either drug. No dose adjustment required (184)

Increase;Decrease; AUC Area under the curve; Cmax Maximum plasma concentration; Cmin Minimum plasma concentration occuring during the dosing interval; Ctrough Minimum plasma concentration immediately before the next dose