| Strength | Formulation | Image | Description | Boosted |
|---|---|---|---|---|
|
DRV 800 mg, COBI 150 mg
|
Film-Coated Tablets
|
Pink, oval-shaped, film-coated tablets debossed with "800" on one side and "TG" on the other side
|
Yes
|
|
|
800 mg
|
Film-Coated Tablets
|
Dark red oval tablet with imprint of 800 on one side and T on the other
|
No
|
|
|
600 mg
|
Film-Coated Tablets
|
Orange oval tablet with imprint of 600MG on one side and TMC on the other.
|
No
|
|
|
150 mg
|
Film-Coated Tablets
|
White oval tablet with imprint of 150 one side and TMC on the other.
|
No
|
|
|
75 mg
|
Film-Coated Tablets
|
White oval tablet with imprint of 75 on one side and TMC on the other.
|
No
|
|
|
100 mg in 1 mL
|
Oral Suspension
|
White to off-white strawberry-flavored solution, 200 mL/bottle
|
No
|
Darunavir
| Interaction Color Code | Clinical Bottom Line | Clinical Effects | Drug 1 effect | Drug 2 dose | Drug 2 effect | Management | |
|---|---|---|---|---|---|---|---|
| Rilpivirine (IM) Darunavir/ritonavir | Green: Administer standard doses | Administer standard doses | |||||
| Darunavir Erythromycin 1033 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of antibacterial adverse effects |
Use alternative agents |
|||
| Darunavir Betrixaban 1032 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased bleeding risk |
No dose adjustment if CrCL < 50 ml / min. Avoid concomitant use if CrCl > 50ml / min. |
|||
| Darunavir Dexamethasone 1031 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential loss of antiviral efficiacy |
Not studied |
Monitor viral load if extended dexamethasone use. Consider alternative corticosteroid for long-term use. |
||
| Darunavir Dextromethrophan 1030 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased dextromethorphan effects |
Not reported |
30 mg x 1 | Cmax increase 127%, AUC increase 170% |
Monitor for dextromethorphan adverse effects |
| Darunavir CBZ 1029 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Increased carbamazepine effects |
Darunavir: No significant change; Ritonavir cmax decreased 44%, AUC decreased 49%, Cmin decreased 56% |
200 mg BID | Cmax increase 43%, AUC increase 45%, Cmin increase 54% |
Monitor anticonvulsant level and adjust accordingly. Consider carbamazepine dose reduction by 25-50%. Monitor antiviral efficacy |
| Darunavir Timolol 1028 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of timolol adverse effects |
If coadministering, use caution and clinical monitoring is recommended |
|||
| Darunavir Metoprolol 1027 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of metoprolol adverse effects |
If coadministering, use caution and clinical monitoring is recommended |
|||
| Darunavir Carvedilol 1026 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of carvedilol adverse effects |
If coadministering, use caution and clinical monitoring is recommended |
|||
| Darunavir Diltiazem 1025 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of diltiazem adverse effects |
If coadministering, titrate to effect and monitor diltiazem adverse effects |
|||
| Darunavir Verapamil 1024 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of verapamil adverse effects |
If coadministering, monitor verapamil adverse effects |
|||
| Darunavir Lidocaine 1023 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of lidocaine adverse effects |
If coadministering use with caution and monitor for lidocaine toxicity. Consider therapeutic drug monitoring and ECG if used systemically. |
|||
| Darunavir Ziprasidone 1022 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of ziprasidone adverse effects |
If coadministering, monitor for adverse effects |
|||
| Darunavir Nefazodone 1021 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of nefazodone adverse effects |
If coadministering, monitor for adverse effects |
|||
| Darunavir Ethosuximide 1020 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of ethosuximide adverse effects |
If coadministering, monitor for adverse effects |
|||
| Darunavir Felodipine 1019 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of felodipine adverse effects (e.g. hypotension, bradycardia) |
If coadministering, monitor felodipine adverse effects |
|||
| Darunavir Quinidine 1018 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of quinidine adverse effects (e.g. cardiac arrhythmias, exacerbation of heart failure) |
If coadministering, monitor and adjust quinidine as indicated |
|||
| Darunavir Nifedipine 1017 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Increased nifedipine effects (e.g. hypotension, bradycardia) |
If coadministering, monitor and adjust nifedipine as indicated |
|||
| Darunavir Nicardipine 1016 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Increased nicardipine effects (e.g. hypotension, heart block) |
If coadministering, monitor and adjust nicardipine as indicated |
|||
| Darunavir Amlodipine 1015 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of amlodipine adverse effects (e.g. hypotension, bradycardia) |
If coadministering, monitor amlodipine adverse effects |
|||
| Darunavir Zolpidem 1014 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of zolpidem adverse effects |
If coadministering, initiate zolpidem at low dose and titrate to effect |
|||
| Darunavir Trazodone 1013 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of trazodone adverse effects (e.g. nausea, dizziness, hypotension, syncope) |
If coadministering, initiate trazodone at low dose. Monitor for CNS and cardiovascular effects. |
|||
| Darunavir Nortiptyline 1012 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of nortriptyline adverse effects |
If coadministering, initiate nortriptyline at low dose. Monitor for CNS and cardiovascular effects. |
|||
| Darunavir CsA 1011 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of cyclosporine adverse effects (supratherapeutic immunosuppression, renal toxicity) |
Not studied |
Not studied (may increase cyclosporine levels) |
If coadministering, initiate lower dose of immunosuppressant, monitor concentrations and toxicity, consult with specialist, and adjust dose as necessary |
|
| Darunavir Imipramine 1010 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of imipramine adverse effects |
If coadministering, initiate imipramine at low dose. Monitor for CNS and cardiovascular effects. |
|||
| Darunavir Estazolam 1009 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of estazolam adverse effects |
If coadministering, initiate estazolam at low dose and titrate to effect |
|||
| Darunavir Diazepam 1008 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of diazepam adverse effects |
If coadministering, initiate diazepam at low dose and titrate to effect |
|||
| Darunavir Desipramine 1007 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of desipramine adverse effects (e.g. nausea, dizziness, hypotension, syncope) |
If coadministering, initiate desipramine at low dose. Monitor for CNS and cardiovascular effects. |
|||
| Darunavir Buspirone 1006 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of busprione adverse effects |
If coadministering, initiate buspirone at low dose and titrate to effect |
|||
| Darunavir Terazosin 1005 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of terazosin adverse effects |
If coadministering, initiate at lowest dose and titrate while monitoring for clinical response / adverse effects |
|||
| Darunavir Doxazosin 1004 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of doxazosin adverse effects |
If coadministering, initiate at lowest dose and titrate while monitoring for clinical response / adverse effects |
|||
| Darunavir Amitriptyline 1003 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of amitriptyline adverse effects |
If coadministering, initiate amitriptyline at low dose. Monitor for CNS and cardiovascular effects. |
|||
| Darunavir Tacrolimus 1002 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of tacrolimus adverse effects |
Not studied |
Not studied (may increase tacrolimus levels) |
If coadministering, consider initiating lower immunosuppressant dose. Therapeutic drug monitoring is recommended. Consult with specialist as necessary. |
|
| Darunavir Sirolimus 1001 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Increased risk of sirolimus adverse effects (supratherapeutic immunosuppression) |
Not studied |
Not studied (may increase rapamycin levels) |
If coadministering, consider initiating lower immunosuppressant dose. Therapeutic drug monitoring is recommended. Consult with specialist as necessary. |
|
| Darunavir Artemether / Lumefantrine 1000 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Clinical significance unknown |
No significant change |
80 / 480 mg | AUC decrease 16%; AUC increase 175% |
If coadministering monitor closely for anti- malarial efficacy and lumefantrine toxicity. Dose adjustment not established. |
| Darunavir Ketoconazole 999 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased darunavir and ketoconazole adverse effects |
200 mg BID | Dose adjustment not established; if co-administration needed, ketoconazole dose should not exceed 200 mg daily |
||
| Darunavir Itraconazole 998 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased darunavir and itraconazole effects |
Dose adjustment not established; if co-administration needed, itraconazole dose should not exceed 200 mg daily |
|||
| Darunavir Posaconazole 997 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of darunavir and posaconazole adverse effects |
Dose adjustment not established, monitor for increased DRV and / or antifungal adverse reactions |
|||
| Darunavir Isavuconazole 996 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of darunavir and isavuconazole adverse effects |
Dose adjustment not established, monitor for increased DRV and / or antifungal adverse reactions |
|||
| Darunavir Drospirenone / Ethinyl estradiol 995 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of drospirenone adverse effects (hyperkalemia) or decreased contraceptive efficacy |
Clinical monitoring is recommended |
|||
| Darunavir Clonazepam 994 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of clonazepam adverse effects |
Clinical monitoring is recommended |
|||
| Darunavir EVG/c 993 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for decreased or increased elvitegravir, cobicistat, and / or darunavir effects |
Cmin decreased 21% |
150 / 150 mg once daily | Elvitegravir AUC decrease 20%, Cmin decrease 52%; Cobicistat AUC decrease 15-20% |
Use alternative agents. One study supports clinical use of elvitegravir / cobicistat with darunavir 800 mg daily in treatment experienced patients. |
| Darunavir Salmeterol 992 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased risk of salmeterol adverse effects |
Use alternative agents |
|||
| Darunavir Alprazolam 991 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased risk of alprazolam adverse effects |
Use alternative agents |
|||
| Darunavir Rivaroxaban 990 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased bleeding risk |
Use alternative agents |
|||
| Darunavir Prasugrel 989 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for decreased antiplatelet activity |
Use alternative agents |
|||
| Darunavir Midazolam 988 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased risk of midazolam adverse effects (e.g. increased sedation, confusion, respiratory depression) |
Parenteral midazolam can be used with caution when given as a single dose in a monitored situation for procedural sedation; chronic midazolam administration (oral or intravenous) is contraindicated |
|||
| Darunavir Tamsulosin 987 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased risk of tamsulosin adverse effects |
If coadministering, monitor for clinical toxicities |
|||
| Darunavir Nilotinib 986 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased risk of nilotinib adverse effects |
If coadministering, decrease dose or adjust dosing interval as needed |
|||
| Darunavir Dasatinib 985 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased risk of dasatinib adverse effects |
If coadministering, decrease dose or adjust dosing interval as needed |
|||
| Darunavir Amiodarone 984 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased risk of amiodarone adverse effects (e.g. hypotension, bradycardia, cardiac arrhythmias) |
If coadministering use with caution. Monitor for amiodarone toxicity. Consider ECG and amiodarone drug level monitoring. |
|||
| Darunavir Apixaban 983 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased bleeding risk |
Do not coadminister in patients who require apixaban 2.5 mg twice daily. In patients requiring apixaban 5 mg or 10 mg twice daily, reduce apixaban dose by 50% |
|||
| Darunavir Quetiapine 982 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased risk of quetiapine adverse effects |
Consider using alternative agents. If coadministering, reduce quetiapine dose to 1 / 6 of current dose and monitor for quetiapine adverse reactions |
|||
| Darunavir Vincristine 981 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased risk of vincristine adverse effects |
Consider temporarily withholding cobicistat-containing ARV regimen in patients who develop significant hematologic or gastrointestinal adverse effects. If ARV regimen must be withheld for a prolonged period of time, initate a revised regimen |
|||
| Darunavir Vinblastine 980 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased risk of vinblastine adverse effects |
Consider temporarily withholding cobicistat-containing ARV regimen in patients who develop significant hematologic or gastrointestinal adverse effects. If ARV regimen must be withheld for a prolonged period of time, initate a revised regimen |
|||
| Darunavir Oxcarbazepine 979 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential loss of antiviral efficacy |
Consider alternate anticonvulsants. If coadministering, use caution and clinical monitoring is recommended |
|||
| Darunavir Eslicarbazepine 978 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential loss of antiviral efficacy |
Consider alternate anticonvulsants. If coadministering, use caution and clinical monitoring is recommended |
|||
| Darunavir Tramadol 977 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased risk of tramadol adverse effects |
Clinical monitoring is recommended. Dose reduction may be needed |
|||
| Darunavir Oxycodone 976 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased risk of oxycodone adverse effects (e.g. respiratory depression) |
Clinical monitoring is recommended |
|||
| Darunavir Fentanyl 975 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased risk of fentanyl adverse effects (e.g. respiratory depression) |
Clinical monitoring is recommended |
|||
| Darunavir Triamcinolone 974 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for decreased plasma cortisol concentrations (e.g. Cushing's syndrome, adrenal suppression) |
Avoid combination or use alternative agents, particularly for long term use |
|||
| Darunavir Mometasone 973 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for decreased plasma cortisol concentrations (e.g. Cushing's syndrome, adrenal suppression) |
Avoid combination or use alternative agents, particularly for long term use |
|||
| Darunavir Methylprednisolone 972 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for decreased plasma cortisol concentrations (e.g. Cushing's syndrome, adrenal suppression) |
Avoid combination or use alternative agents, particularly for long term use |
|||
| Darunavir Ciclesonide 971 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for decreased plasma cortisol concentrations (e.g. Cushing's syndrome, adrenal suppression) |
Avoid combination or use alternative agents, particularly for long term use |
|||
| Darunavir Betamethasone 970 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for decreased plasma cortisol concentrations (e.g. Cushing's syndrome, adrenal suppression) |
Avoid combination or use alternative agents, particularly for long term use |
|||
| Darunavir Budesonide 969 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for decreased plasma cortisol concentrations (e.g. Cushing's syndrome, adrenal suppression) |
Avoid combination or use alternative agents, particularly for long term use |
|||
| Darunavir Fluticasone 968 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for decreased plasma cortisol concentrations (e.g. Cushing's syndrome, adrenal suppression) |
Avoid combination or use alternative agents |
|||
| Darunavir Rivaroxaban 967 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased bleeding risk |
Avoid combination; use alternative anticoagulant |
|||
| Darunavir Apixaban 966 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased bleeding risk |
Avoid combination; use alternative anticoagulant |
|||
| Darunavir Vorapaxar 965 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased bleeding risk |
Avoid combination and use alternative antiplatelet agent |
|||
| Darunavir Ticagrelor 964 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased bleeding risk |
Avoid combination and use alternative antiplatelet agent |
|||
| Darunavir Dabigatran 963 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased bleeding risk |
Avoid combination and use alternative anticoagulant |
|||
| Darunavir Phenytoin 962 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential loss of antiviral efficacy, Potential for decreased phenytoin effects |
Avoid combination and use alternative agents. If coadministering, monitor and adjust phenytoin levels as indicated and monitor viral load. |
|||
| Darunavir Phenobarbital 961 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential loss of antiviral efficacy, Potential for decreased phenobarbital effects |
Avoid combination and use alternative agents. If coadministering, monitor and adjust phenytoin levels as indicated and monitor viral load. |
|||
| Darunavir Voriconazole 960 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential decreased voriconazole effects |
Avoid coadministering with boosted protease inhibitors unless benefit outweighs risks. If coadministering, consider therapeutic drug monitoring. |
|||
| Darunavir Ethinyl estradiol / Norethindrone acetate 959 | Red: Avoid combination | Do not coadminister: Reduced levels of ethinyl estradiol and norethindrone | Potential decreased ethinyl estradiol and norethindrone effects (e.g. contraceptive failure) |
No significant change |
35 mcg / 1.0 mg once daily | Ethinyl estradiol: Cmax decrease 32%, AUC decrease 44%, Cmin decrease 62%; Norethindrone: Cmax decrease 10%, AUC decrease 14%, Cmin decrease 30% |
Use alternative agents. If coadministering, back-up contraceptive methods are recommended. |
| Darunavir Dasabuvir + Ombitasvir / Paritaprevir / Ritonavir 958 | Red: Avoid combination | Do not coadminister: Reduced levels of darunavir | Potential decreased anti-HCV and anti-HIV efficacy |
Darunavir Cmax decreased 8%; AUC decreased 24%; Cmin decreased 48% |
250 mg BID + 25 / 150 / 100 mg once daily | Dasabuvir Cmax increase 10%, AUC decrease 6%, Cmin increase 10%; Ombitasvir Cmax and AUC decrease 14%, Cmin decrease 13%; Paritaprevir Cmin increase 54%, AUC increase 29%, Cmin increase 30% |
Use alternative agents |
| Darunavir Dasabuvir + Ombitasvir / Paritaprevir / Ritonavir 957 | Red: Avoid combination | Do not coadminister: Reduced levels of darunavir | Potential decreased anti-HCV and anti-HIV efficacy |
Cmax decrease 21%, AUC increase 34%, Cmin decrease 46% |
250 mg BID + 25 / 150 / 100 mg once daily | Dasabuvir Cmax decrease 25%, AUC decrease 28%, Cmin decrease 35%; Ombitasvir Cmax, AUC, and Cmin decrease 13%; Paritaprevir Cmax decrease 30%, AUC decrease 19%, Cmin increase 59% |
Use alternative agents |
| Darunavir Dasabuvir + Ombitasvir / Paritaprevir / Ritonavir 956 | Red: Avoid combination | Do not coadminister: Reduced levels of darunavir | Potential decreased anti-HCV and anti-HIV efficacy |
Cmax decrease 13%, AUC decrease 20%, Cmin decrease 43% |
250 mg BID + 25 / 150 / 100 mg once daily | Dasabuvir Cmax decrease 16%, AUC decrease 27%; Cmin decrease 46%; Ombitasvir Cmax decrease 24%, AUC and Cmin decrease 27%; Paritaprevir Cmax decrease 30%, AUC decrease 41%, Cmin decrease 17% |
Use alternative agents |
| Darunavir Phenytoin 955 | Red: Avoid combination | Do not coadminister: Potential for reduced levels of darunavir | Potential loss of antiviral efficacy |
Contraindicated. Use alternative agents. |
|||
| Darunavir Phenobarbital 954 | Red: Avoid combination | Do not coadminister: Potential for reduced levels of darunavir | Potential loss of antiviral efficacy |
Contraindicated. Use alternative agents. |
|||
| Darunavir St. John's Wort (Hypericum perforatum) 953 | Red: Avoid combination | Do not coadminister: Potential for reduced levels of darunavir | Potential loss of antiviral efficacy |
Contraindicated. Use alternative agents. |
|||
| Darunavir CBZ 952 | Red: Avoid combination | Do not coadminister: Potential for reduced levels of darunavir | Potential loss of antiviral efficacy |
Contraindicated. Use alternative agents. |
|||
| Darunavir RIF 951 | Red: Avoid combination | Do not coadminister: Potential for reduced levels of darunavir | Potential loss of antiviral efficacy |
Contraindicated. Use alternative agents. |
|||
| Darunavir Suvorexant 950 | Red: Avoid combination | Do not coadminister: Potential for increased suvorexant levels | Potential for increased risk of suvorexant adverse effects |
Use alternative agents |
|||
| Darunavir Perphenazine 949 | Red: Avoid combination | Do not coadminister: Potential for increased perphenazine levels | Potential for increased risk of perphenazine adverse effects |
Contraindicated. Use alternative agents. |
|||
| Darunavir Naloxegol 948 | Red: Avoid combination | Do not coadminister: Potential for increased naloxegol levels | Potential for increased risk of precipitating opioid withdrawal |
Contraindicated. Use alternative agents. |
|||
| Darunavir Mexiletine 947 | Red: Avoid combination | Do not coadminister: Potential for increased mexiletine levels | Potential for increased risk of mexiletine adverse effects |
Use alternative agents |
|||
| Darunavir Lurasidone 946 | Red: Avoid combination | Do not coadminister: Potential for increased lurasidone levels | Potential for increased risk of lurasidone adverse effects |
Contraindicated. Use alternative agents. |
|||
| Darunavir Triazolam 945 | Red: Avoid combination | Do not coadminister: Potential for increased levels of triazolam | Potential for increased risk of triazolam adverse effects (e.g. increased sedation, confusion, respiratory depression) |
Contraindicated. Use alternative agents. |
|||
| Darunavir Terfenadine 944 | Red: Avoid combination | Do not coadminister: Potential for increased levels of terfendaine | Potential for increased risk of terfenadine adverse effects (e.g. cardiac arrhythmias) |
Use alternative agents |
|||
| Darunavir Simvastatin 943 | Red: Avoid combination | Do not coadminister: Potential for increased levels of simvastatin | Increased risk of simvastatin adverse effects (e.g. myopathy, rhabdomyolysis) |
Not studied |
Not studied (may increase simvastatin levels) |
Contraindicated. Use alternative agents. |
|
| Darunavir Silodosin 942 | Red: Avoid combination | Do not coadminister: Potential for increased levels of silodosin | Potential for increased risk of silodosin adverse effects |
Contraindicated. Use alternative agents. |
|||
| Darunavir Ranolazine 941 | Red: Avoid combination | Do not coadminister: Potential for increased levels of ranolazine and darunavir | Potential for increased risk of ranolazine adverse effects (e.g. prolonged QT, cardiac arrythmias) |
Use alternative agents |
|||
| Darunavir Pimozide 940 | Red: Avoid combination | Do not coadminister: Potential for increased levels of pimozide | Potential for increased risk of pimozide adverse effects (e.g. hypotension, cardiac arrhythmias) |
Contraindicated. Use alternative agents. |
|||
| Darunavir HMG-CoA Reductase Inhibitors 939 | Red: Avoid combination | Do not coadminister: Potential for increased levels of lovastatin | Increased risk of lovastatin adverse effects (e.g. myopathy, rhabdomyolysis) |
Not studied |
Not studied (may increase lovastatin levels) |
Contraindicated. Use alternative agents. |
|
| Darunavir Lomitapide 938 | Red: Avoid combination | Do not coadminister: Potential for increased levels of lomitapide | Potential for increased risk of lomitapide adverse effects |
Not studied |
Not studied |
Contraindicated. Use alternative agents. |
|
| Darunavir Ergotamine 937 | Red: Avoid combination | Do not coadminister: Potential for increased levels of ergotamine | Potential for increased risk of ergotamine adverse effects (e.g. peripheral vasospasm, ischemia) |
Contraindicated. Use alternative agents. |
|||
| Darunavir Dofetilide 936 | Red: Avoid combination | Do not coadminister: Potential for increased levels of dofetilide | Potential for increased risk of dofetilide adverse effects |
Use alternative agents |
|||
| Darunavir Disopyramide 935 | Red: Avoid combination | Do not coadminister: Potential for increased levels of disopyramide | Potential for increased risk of disopyramide adverse effects |
Use alternative agents |

