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| Interaction | In vitro results suggest that abacavir is not metabolized by the cytochrome enzymes. An interaction with amprenavir doesn't look likely to happen. |
| Recommendation | No specific action is required. |
| References | 129,130,131 |
| Interaction | In vitro results suggest that abacavir is not metabolized by the cytochrome enzymes. An interaction with amprenavir doesn't look likely to happen. |
| Recommendation | No specific action is required. |
| References | 129 |
| Interaction | The AUC of lamivudine decreases by 15%, but this doesn't lead to a clinically significant drug interaction. |
| Recommendation | No specific action is required. |
| References | 131,132 |
| Interaction | In vitro results suggest that abacavir is not metabolized by the cytochrome enzymes. An interaction with nelfinavir doesn't look likely to happen. |
| Recommendation | No specific action is required. |
| References | 129 |
| Interaction | In vitro results suggest that abacavir is not metabolized by the cytochrome enzymes. An interaction with amprenavir doesn't look likely to happen. |
| Recommendation | No specific action is required. |
| References | 129 |
| Interaction | In vitro results suggest that abacavir is not metabolized by the cytochrome enzymes. An interaction with saquinavir doesn't look likely to happen. |
| Recommendation | No specific action is required. |
| References | 129,130 |
| Interaction | The AUC of zidovudine increases by 24%, but this doesn't lead to a clinically significant drug interaction. |
| Recommendation | No specific action is required. |
| References | 129,131 |
| Interaction | Efavirenz induces CYP3A4. This results in a decrease
of the AUC of amprenavir by 36%, of his Cmax by 39% and of his Cmin by
45%.
The AUC of efavirenz increases by 15%. This doesn't lead to a clinically significant drug interaction. |
| Recommendation | No adjustment of dosage necessary. |
| References | 131,133 |
| Interaction | The AUC of indinavir decreases by 38%, his Cmin decreases by 27% and
his Cmax by 22%.
The AUC of amprenavir increases by 22 to 26% This doesn't lead to a clinically significant drug interaction. |
| Recommendation | No adjustment of dosage necessary. |
| References | 131,133,134 |
| Interaction | There is no clinically significant drug interaction. |
| Recommendation | No specific action is required. |
| References | 131 |
| Interaction | The AUC of amprenavir isn't affected but his Cmin increases by 167%.
The AUC of nelfinavir increases by 15%. |
| Recommendation | No adjustment of dosage necessary. |
| References | 131 |
| Interaction | The AUC of amprenavir increases by 700% and his Cmax by 80%. This is the result of the inhibition of metabolization (CYP-enzymes) by ritonavir. |
| Recommendation | no info |
| References | 130 |
| Interaction | Saquinavir (soft gel) decreases the AUC of amprenavir by 36%.
The AUC of saquinavir (sot gel) decreases by 18%. |
| Recommendation | No adjustment of dosage should be necessary, but monitor the clinical efficacy of this combination and adjust the dose if necessary. |
| References | 131 |
| Interaction | The AUC of zidovudine increases by 31%, but this doesn't lead to a clinically significant drug interaction. |
| Recommendation | No adjustment of dosage necessary. |
| References | 131 |
| Interaction | The AUC of delavirdine decreases by 22% to 28% and his Cmax decreases
by 53%.
The AUC of didanosine decreases by 17% to 20%. |
| Recommendation | Space the administration of delavirdiner and didanosine by at least 1 hour. |
| References | 135,136,137,131,132,133,138,139 |
| Interaction | The AUC of indinavir increases by 40% to 100%, his Cmax decreases and his Cmin increases. This is the result of the CYP3A4 inhibition by delavirdine. |
| Recommendation | Adjustment in dosage are necessary (Decrease the dose of indinavir to 600mg) |
| References | 137,131,133,134,140 |
| Interaction | The AUC of delavirdine decreases by 42%, but this doesn't lead to a clinically significant drug interaction. |
| Recommendation | No specific action is required. |
| References | 141,142 |
| Interaction | The AUC of delavirdine decreases by 42%, his Cmax by 34%.
The AUC of nelfinavir increases by 90% to 100%. This probably doesn't lead to a clinically significant drug interaction. |
| Toxicity | Concomitant use can lead to increased incidence of neutropenia and leukopenia.. |
| Recommendation | Pobably no adjustment of dosage necessary, but monitor blood work and signs and symptoms of neutropenia and leukopenia. |
| References | 142,143,131,133 |
| Interaction | The AUC of ritonavir increases by 70% to 78%, presumably through inhibition of ritonavir oxidative metabolism. |
| Recommendation | Adjustment in dosage are necessary |
| References | 131,133,132 |
| Interaction | The AUC of saquinavir increases by 400% and the AUC of delavirdine decreases by 24%. |
| Recommendation | Adjustment in dosage are necessary |
| References | 135 |
| Interaction | The buffered vehicle for didanosine (i.e., a magnesium/aluminum antacid) produces an acutely alkaline gastric environment that may decrease the absorption of indinavir, which needs a acidic environment for absorption. |
| Recommendation | Space the administration of indinavir and didanosine by at least 1 hour. Preferably, administer indinavir 1 before or 2 hour(s) after didanosine. |
| References | 135,136,137,141,144 |
| Interaction | There is no clinically significant drug interaction. |
| Recommendation | No specific action is required. |
| References | 141 |
| Interaction | There is no clinically significant drug interaction. |
| Recommendation | Because didanosine should be taken without food and nelfinavir with food, nelfinavir should be administered 2 hours before or 1 hour after didanosine. |
| References | 142,143,132 |
| Interaction | There is no clinically significant drug interaction. |
| Recommendation | No adjustment of dosage necessary. |
| References | 145,146 |
| Interaction | Ritonavir seems to reduce didanosine bioavailability. The AUC of didanosine decreases by 13% and its Cmax by 16% . This doesn't seem to lead to a clinically significant drug interaction. |
| Recommendation | No adjustment of dosage necessary.
Space the administration of ritonavir and didanosine by at least 2,5 hours to avoid interactions between both formulations.. |
| References | 135,147,137,148,131,132 |
| Interaction | There is no clinically significant drug interaction. |
| Toxicity | Concomitant use can lead to an increased risk of peripheral neuropathy. |
| Recommendation | No adjustment of dosage necessary, but monitor for signs and symptoms of peripheral neuropathy: numbness, burning dysesthesia and weakness involving the distal extremeties, tingling. |
| References | 136,147,141,133,138,149 |
| Interaction | There is no clinically significant drug interaction. |
| Toxicity | Concomitant use can lead to an increased risk of peripheral neuropathy and pancreatitis. |
| Recommendation | Concomitant use is dissuaded
Monitor for signs and symptoms of peripheral neuropathy: numbness, burning dysesthesia and weakness involving the distal extremeties, tingling. Monitor for signs and symptoms of pancreatitis (abdominal pain, nausea, vomiting). Monitor amylases and lipases concentrations monthly. |
| References | 135,136,137,141,133,139,150,151,152 |
| Interaction | The AUC of didanosine decreases by 19% and the AUC of zidovudine increases by 35%, but this doesn't lead to a clinically significant drug interaction. |
| Toxicity | Concomitant use can lead to an increased risk of peripheral neuropathy. |
| Recommendation | No adjustment of dosage necessary, but monitor for signs and symptoms of peripheral neuropathy: numbness, burning dysesthesia and weakness involving the distal extremeties, tingling. |
| References | 147,138,139,151,153,154 |
| Interaction | As a result of the CYP3A4 induction of efavirenz, the AUC of indinavir decreases by 30% to 35% and the Cmax decreases by 16%. |
| Recommendation | Adjustment in dosage are necessary (it is recommended to increase the dose of indinavir to 1000 mg) |
| References | 131,133,134,155 |
| Interaction | There is no clinically significant drug interaction. |
| Recommendation | No specific action is required. |
| References | 131,155 |
| Interaction | There is no clinically significant drug interaction. |
| Recommendation | No specific action is required. |
| References | 143 |
| Interaction | The AUC of efavirenz increases by 21% and the AUC of ritonavir increases by 17% to 18%. |
| Recommendation | Adjustment in dosage are necessary (it is recommended
to decrease the dose of ritonavir to 500 mg)
Monitor the liver enzymes of patients. |
| References | 155 |
| Interaction | There is no clinically significant drug interaction. |
| Recommendation | No specific action is required. |
| References | 131,155 |
| Interaction | The AUC of lamivudine decreases by 6%, but this doesn't lead to a clinically significant drug interaction. Both drugs have different metabolisation pathways. |
| Recommendation | No specific action is required. |
| References | 135,141,132 |
| Interaction | Nelfinavir decreases the elimination of indinavir, which causes an
increase of the AUC of indinavir by 51%
The AUC of nelfinavir increases by 83% to 84% and his Cmax increases by 31%. This is caused by an inhibition of CYP3A. |
| Recommendation | no info |
| References | 142,143,134 |
| Interaction | Nevirapine decreases the AUC of indinavir by 25 to 30%, his Cmax by
11% and his Cmin 38%. This is the result of the CYP3A4
induction by nevirapine.
The nevirapine AUC decreases less than 10%. The clinical significance of this interaction is unknown. |
| Recommendation | Concomitant use is dissuaded till new research brings
clearness.
Adjustment in dosage are necessary (it is recommended to increase the dose of indinavir to 1000 mg and monitor for signs and symptoms of indinavir therapeutic failure.) |
| References | 135,137,141,156,131,133,145 |
| Interaction | Ritonavir inhibits the metabolisation of indinavir.This results in an increase of the AUC of indinavir by 200% to 500%. |
| Recommendation | Adjustment in dosage are necessary (Indinavir and ritonavir both 400mg 2x a day) |
| References | 131,133,134,157 |
| Interaction | Indinavir may inhibit the hepatic metabolism of saquinavir. The AUC of saquinavir increases by 360% to 620 % and his Cmax by 551% |
| Recommendation | Adjustment in dosage are necessary |
| References | 135,158,131,133,134 |
| Interaction | The AUC of stavudine is increases by 25% whereas the AUC indinavir remains unchanged, but this doesn't lead to a clinically significant drug interaction. |
| Recommendation | No dosage adjustment is necessary. |
| References | 135,147,141,132 |
| Interaction | The AUC of zidovudine increases by 17% to 35% and the AUC of indinavir increases by 13%, but this doesn't lead to a clinically significant drug interaction. |
| Recommendation | No dosage adjustment is necessary. |
| References | 135,147,132 |
| Interaction | The AUC of lamivudine increased by 10% and the Cmax increased by 31%, but this doesn't lead to a clinically significant drug interaction. Both drugs have different metabolisation pathways. |
| Recommendation | No specific action is required. |
| References | 135,141,142,143 |
| Interaction | There is no clinically significant drug interaction. |
| Recommendation | No specific action is required. |
| References | 141,145 |
| Interaction | There is no clinically significant drug interaction. Both drugs have different elimination routes. |
| Recommendation | No specific action is required. |
| References | 141 |
| Interaction | There is no clinically significant drug interaction, but due to the competion for the same enzyme the phosphorylation of zalcitabine in vitro was decreased. |
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|
Concomitant administration can lead to an increased risk of peripheral neuropathy. |
| Recommendation | No adjustment of dosage necessary, but monitor for signs and symptoms of peripheral neuropathy: numbness, burning dysesthesia and weakness involving the distal extremeties, tingling. |
| References | 141,133,159 |
| Interaction | The Cmax of zidovudine increases, but this doesn't lead to a clinically significant drug interaction. |
| Recommendation | No adjustment of dosage necessary. |
| References | 135,147,141,138,144,159 |
| Interaction | The AUC of nelfinavir decreases by 10% to 20% |
| Recommendation | Adjustment in dosage are necessary (Increase the dose of nelfinavir from 750mg to 1000mg 3x a day) |
| References | 137,141,143,131,160 |
| Interaction | Ritonavir inhibits the metabolisation nelfinavir. The AUC of ritonavir remaines unchanged. The AUC of nelfinavir increased by 152%. |
| Recommendation | Adjustment in dosage are necessary (ritonavir 400mg 2x a day and nelfinavir 750mg 2x a day) |
| References | 135,142,143 |
| Interaction | Nelfinavir inhibits CYP3A4 and this results in
an increase of saquinavir concentrations. The AUC of saquinavir increases
by 400% (soft gel) and from 400 to 1150% (hard gel).
The AUC of nelfinavir increases with 17%. (with soft gel) Nelfinavir also decreases the elimination of saquinavir. |
| Recommendation | Adjustment in dosage are necessary for Fortovase® (soft gel)
No adjustment of dosage necessary for Invirase® (hard gel) |
| References | 135,156,142,143,158,131,133 |
| Interaction | There is no clinically significant drug interaction. |
| Recommendation | No specific action is required. |
| References | 141,142,143 |
| Interaction | There is no clinically significant drug interaction. |
| Recommendation | No specific action is required. |
| References | 143 |
| Interaction | The AUC and Cmax of zidovudine decreased by more than 35%, but this doesn't lead to a clinically significant drug interaction. |
| Recommendation | No specific action is required. |
| References | 135,142,143,131 |
| Interaction | The AUC of ritonavir decreases by 11%, his Cmax by 11% and Cmin by
9%. This is result of the induction of the metabolisation of ritonavir
by nevirapine.
This doesn't lead to a clinically significant drug interaction. |
| Recommendation | No specific action is required. |
| References | 135,156,142,145 |
| Interaction | Nevirapine induces CYP3A4 and this results in an 27% increase of the AUC of saquinavir. |
| Recommendation | Adjustment in dosage are necessary (Increase the dose of saquinavir) |
| References | 135,137 |
| Interaction | There is no clinically significant drug interaction. |
| Recommendation | No specific action is required. |
| References | 141,145 |
| Interaction | There is no clinically significant drug interaction. |
| Recommendation | No adjustment of dosage necessary. |
| References | 132 |
| Interaction | There is no clinically significant drug interaction. |
| Recommendation | No adjustment of dosage necessary. |
| References | 145,146 |
| Interaction | Ritonavir may inhibit the hepatic metabolism of saquinavir (CYP3A4).
The AUC of saquinavir increases by more then 2000%.
The AUC and Cmax of ritonavir remains unchanged. |
| Recommendation | Adjustment in dosage are necessary (Decrease the dose of ritonavir and saquinavir to 400mg 2x a day) |
| References | 135,158,131,133,132,134,157,161,162,163 |
| Interaction | There is no clinically significant drug interaction. |
| Recommendation | No specific action is required. |
| References | 141 |
| Interaction | Ritonavir may decrease the bioavailability of zidovudine, because it reduces the AUC of zidovudine by 25%. The clinical significance of this interaction is unknown. |
| Recommendation | No adjustment of dosage should be necessary, but monitor the clinical efficacy of this combination and increase the dose of zidovudine if necessary. |
| References | 135,147,148,131,132 |
| Interaction | There is no clinically significant drug interaction. Both drugs have different elimination routes. |
| Recommendation | No specific action is required. |
| References | 132 |
| Interaction | There is no clinically significant drug interaction. |
| Recommendation | No specific action is required. |
| References | 132 |
| Interaction | There is no clinically significant drug interaction. |
| Toxicity | Concomitant use can lead to an increased risk of peripheral neuropathy. |
| Recommendation | No adjustment of dosage necessary, but monitor for signs and symptoms of peripheral neuropathy: numbness, burning dysesthesia and weakness involving the distal extremeties, tingling. |
| References | 136,141,133,149,152,164 |
| Interaction | The phosphorylation of stavudine is decreased by zidovudine. |
| Recommendation | Concomitant use is dissuaded |
| References | 136,164 |
| Interaction | There is no clinically significant drug interaction. |
| Recommendation | No adjustment of dosage necessary. |
| References | 147,138,,150,152,154,165 |
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