EVG is only available as a component of an STR tablet that also contains COBI, FTC, and either TDF or TAF (Stribild, Genvoya).
Elvitegravir
| Interaction Color Code | Clinical Bottom Line | Clinical Effects | Drug 1 effect | Drug 2 dose | Drug 2 effect | Management | |
|---|---|---|---|---|---|---|---|
| Elvitegravir Erythromycin 280 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Use alternative agents |
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| Elvitegravir Nefazodone 279 | 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 |
Use alternative agents |
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| Elvitegravir Dexamethasone 278 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential loss of antiviral efficacy |
Monitor viral load if extended dexamethasone use. Consider alternative corticosteroid for long-term use. |
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| Elvitegravir Eluxadoline 277 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of eluxadoline adverse effects |
Monitor response and titrate according to efficacy and adverse effects. |
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| Elvitegravir Itraconazole 276 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased adverse effects from both elvitegravir and itraconazole |
Monitor itraconazole concentrations. If coadministering itraconazole dose should not exceed 200 mg daily unless guided by concentrations. |
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| Elvitegravir Tramadol 275 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased sedation |
Initiate tramadol at lowest dose. If initiating elvitegravir / cobicistat, tramadol may require a dose reduction - monitor for efficacy and adverse effects to titrate. |
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| Elvitegravir Fentanyl 274 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of sedation and respiratory depression |
If coadministering, titrate carefully and monitor for sedation and respiratory depression |
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| Elvitegravir Posaconazole 273 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | If coadministering, monitor posaconazole concentrations. |
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| Elvitegravir Ketoconazole 272 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased adverse effects from both elvitegravir and ketoconazole |
If coadministering, ketoconazole dose should not exceed 200 mg daily. |
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| Elvitegravir CsA 271 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased cyclosporine toxicity |
Not reported |
If coadministering, initiate lower dose of immunosuppressant, therapeutic drug monitoring is recommended, assess toxicity, consult with specialist, and adjust dose as necessary |
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| Elvitegravir Tacrolimus 270 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Increased tacrolimus adverse effects (increased immunosuppression) |
If coadministering, initiate lower dose of immunosuppressant, therapeutic drug monitoring is recommended, assess toxicity, consult with specialist, and adjust dose as necessary |
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| Elvitegravir Sirolimus 269 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Increased sirolimus adverse effects (increased immunosuppression) |
If coadministering, initiate lower dose of immunosuppressant, therapeutic drug monitoring is recommended, assess toxicity, consult with specialist, and adjust dose as necessary |
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| Elvitegravir Propafenone 268 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of propafenone adverse effects |
If coadministering use with caution and monitor for propafenone toxicity. Consider therapeutic drug monitoring and ECG |
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| Elvitegravir Mexiletine 267 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of mexiletine adverse effects |
If coadministering use with caution and monitor for mexiletine toxicity. Consider therapeutic drug monitoring and ECG |
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| Elvitegravir Lidocaine 266 | 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. |
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| Elvitegravir Flecainide 265 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of flecainide adverse effects (eg, cardiac arrhythmias) |
If coadministering use with caution and monitor for flecainide toxicity. Consider therapeutic drug monitoring and ECG |
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| Elvitegravir Disopyramide 264 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of disopyramide adverse effects |
If coadministering use with caution and monitor for disopyramide toxicity. Consider therapeutic drug monitoring and ECG |
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| Elvitegravir Amiodarone 263 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased amiodarone effects (eg, hypotension, bradycardia, cardiac arrhythmias) |
If coadministering use with caution and monitor for amiodarone toxicity. Consider therapeutic drug monitoring and ECG. |
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| Elvitegravir Verapamil 262 | 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 use with caution and monitor ECG |
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| Elvitegravir Nifedipine 261 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of nifedipine adverse effects |
If coadministering use with caution and monitor ECG |
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| Elvitegravir Nicardipine 260 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of nicardipine adverse effects |
If coadministering use with caution and monitor ECG |
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| Elvitegravir Felodipine 259 | 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 |
If coadministering use with caution and monitor ECG |
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| Elvitegravir Diltiazem 258 | 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 use with caution and monitor ECG |
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| Elvitegravir Amlodipine 257 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of amlodopine adverse effects |
If coadministering use with caution and monitor ECG |
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| Elvitegravir Lofexidine 256 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of lofexidine adverse effects (e.g. orthostasis and bradycardia) |
If coadministering use with caution and monitor blood pressure, heart rate, and dizziness. |
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| Elvitegravir Fluoxetine 255 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of fluoxetine adverse effects |
If coadministering start with lowest fluoxetine dose. Monitor response and titrate dose according to efficacy and adverse effects |
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| Elvitegravir Ziprasidone 254 | 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 start with low dose and titrate accordingly. Monitor for side effects. |
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| Elvitegravir Zolpidem 253 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of sedative-hypnotic adverse effects |
If coadministering start with low dose and titrate accordingly. Monitor for side effects. |
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| Elvitegravir Flurazepam 252 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of sedative-hypnotic adverse effects |
If coadministering start with low dose and titrate accordingly. Monitor for side effects. |
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| Elvitegravir Estazolam 251 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of sedative-hypnotic adverse effects |
If coadministering start with low dose and titrate accordingly. Monitor for side effects. |
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| Elvitegravir Diazepam 250 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of sedative-hypnotic adverse effects |
If coadministering start with low dose and titrate accordingly. Monitor for side effects. |
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| Elvitegravir Clorazepate 249 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of sedative-hypnotic adverse effects |
If coadministering start with low dose and titrate accordingly. Monitor for side effects. |
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| Elvitegravir Isavuconazole 248 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | If coadministering monitor isavuconazole concentrations and assess virologic response. |
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| Elvitegravir Warfarin 247 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential over or under anticoagulation |
If coadministering monitor INR and adjust warfarin as indicated. Monitor for signs and symptons of bleeding. |
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| Elvitegravir Dronedarone 246 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of dronedarone adverse effects |
If coadministering monitor for dronedarone toxicity. Consider therapeutic drug monitoring and ECG. |
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| Elvitegravir Prednisone 245 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of adrenal insufficiency and Cushing's syndrome, but PK / PD less affected by strong CYP3A4 inhibitors |
If coadministering monitor for adrenal insufficiency and Cushing's syndrome |
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| Elvitegravir Everolimus 244 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Increased everolimus effects (e.g. excessive immunosuppression) |
If coadministering monitor everolimus levels and adjust dose as indicated |
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| Elvitegravir Citalopram 243 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased SSRI adverse effects |
If coadministering initiate therapy with lowest citalopram dose. Monitor citalopram response and titrate dose according to efficacy and adverse effects. |
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| Elvitegravir Escitalopram 242 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential increase in SSRI adverse effects |
If coadministering initiate escitalopram therapy with lowest dose. Monitor escitalopram response and titrate according to efficacy and adverse effects |
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| Elvitegravir Dronabinol 241 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of dronabinol adverse effects (e.g. sedation) |
If coadministering initiate dronabinol at lowest dose. Monitor response and titrate according to efficacy and adverse effects. |
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| Elvitegravir Prednisolone 240 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of adrenal insufficiency and Cushing's syndrome, but PK / PD less affected by strong CYP3A4 inhibitors |
If coadministering for systemic use, monitor for adrenal insufficiency and Cushing's syndrome. Do not coadminister if prednisolone needed for local injections. |
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| Elvitegravir Voriconazole 239 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | If coadministering assess risk and benefit. Consider monitoring voriconaozle concentrations. |
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| Elvitegravir Ciclesonide 238 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of adrenal insufficiency and Cushing's syndrome |
If coadministering assess risk and benefit |
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| Elvitegravir Dutasteride 237 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of dutasteride adverse effects |
If coadministering adjust dutasteride dose based on clinical effects and endogenous hormone concentrations. |
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| Elvitegravir Dabigatran 236 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of bleeding |
Dosing depends on indication and renal function. For DVT and PE, avoid co-administration if CrCL < 50 mL / min. For stroke and embolism prevention in persons with atrial fibrillation, do not coadminister in severe renal insufficiency (CrCL< 30mL / min) and consider dose reduction to 75 mg twice daily if CrCL between 30 - 50mL / min |
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| Elvitegravir Fluvoxamine 235 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential decreased elvitegravir effects |
Consider using alternative antidepressant |
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| Elvitegravir Quetiapine 234 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of quetiapine adverse effects |
Consider alternative ARV therapy. For patients currently on elvitegravir / cobicistat: initiate quetiapine at lowest dose. Titrate accordingly and monitor for adverse effects. If patient already on quetiapine and requiring new elvitegravir / cobicistat: reduce queitapine to 1 / 6 of original dose before coadministering. Monitor efficacy and adverse effects. |
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| Elvitegravir Timolol 233 | 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 |
Consider alternative agents. If coadministering initiate beta-blocker at low dose and titrate to clinical effect while monitoring for adverse effects. |
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| Elvitegravir Metoprolol 232 | 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 |
Consider alternative agents. If coadministering initiate beta-blocker at low dose and titrate to clinical effect while monitoring for adverse effects. |
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| Elvitegravir Betrixaban 231 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of bleeding |
Administer single dose of betrixaban 80 mg, followed by betrixaban 40 mg once daily |
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| Elvitegravir Testosterone 230 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: weigh risks and benefits of using this combination | Potential for increased risk of testosterone adverse effects |
Adjust testosterone dose based on clinical effects and endogenous hormone concentrations. |
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| Elvitegravir Oxcarbazepine 229 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential decrease in antiretroviral efficacy |
Use alternative agents |
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| Elvitegravir Budesonide 228 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased risk of adrenal insufficiency and Cushing's syndrome |
Use alternative agents |
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| Elvitegravir Tamsulosin 227 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased tamulosin adverse effects |
Use alternate agents. If coadministering, use with caution and monitor for tamulosin related adverse effects |
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| Elvitegravir Quinidine 226 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased risk of quinidine adverse effects (e.g. cardiac arrhythmias) |
If coadministering use with caution and monitor for quinidine toxicity. Consider therapeutic drug monitoring and ECG |
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| Elvitegravir Betamethasone 225 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased risk of adrenal insufficiency and Cushing's syndrome |
Do not coadminister if betamethasone used for local injection. |
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| Elvitegravir Apixaban 224 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased risk of bleeding |
Consider avoiding combination and using alternative anticoagulant. If coadministering, reduce apixaban dose by 50% in patients who require 5-10 mg twice daily. Do not coadminister in persons who require apixaban 2.5mg twice daily. |
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| Elvitegravir Rivaroxaban 223 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased risk of bleeding |
Avoid combination and use alternative anticoagulant |
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| Elvitegravir Ethinyl estradiol / Drospirenone 222 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential for increased drospirenone effects (hyperkalemia); Potential decreased ethinyl estradiol effects |
Additional or alternative contraception should be considered. If using, monitor potassium. |
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| Elvitegravir LNG 221 | Orange: Minimal data to guide interaction | Minimal data to guide interaction: risks likely to outweigh benefits | Potential increase in levonorgestrel adverse effects |
Additional or alternative contraception should be considered. |
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| Elvitegravir RPT 220 | Red: Avoid combination | Do not coadminister: Potential for reduced levels of elvitegravir | Potential decrease in antiretroviral efficacy |
Use alternative agents |
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| Elvitegravir St. John's Wort (Hypericum perforatum) 219 | Red: Avoid combination | Do not coadminister: Potential for reduced levels of elvitegravir | Potential decrease in antiretroviral efficacy |
Contraindicated. Use alternative agents. |
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| Elvitegravir Eslicarbazepine 218 | Red: Avoid combination | Do not coadminister: Potential for reduced levels of elvitegravir | Potential decrease in antiretroviral efficacy |
Contraindicated. Use alternative agents. |
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| Elvitegravir Phenytoin 217 | Red: Avoid combination | Do not coadminister: Potential for reduced levels of elvitegravir | Potential decrease in antiretroviral efficacy |
Contraindicated. Use alternative agents. |
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| Elvitegravir Phenobarbital 216 | Red: Avoid combination | Do not coadminister: Potential for reduced levels of elvitegravir | Potential decrease in antiretroviral efficacy |
Contraindicated. Use alternative agents. |
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| Elvitegravir RIF 215 | Red: Avoid combination | Do not coadminister: Potential for reduced levels of elvitegravir | Expected significant decreased in elvitegravir, cobicistat. Potential decreased antiretroviral efficacy |
Contraindicated. Use alternative agents. |
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| Elvitegravir Clopidogrel 214 | Red: Avoid combination | Do not coadminister: Potential for reduced levels of clopidogrel | Potential reduction of antiplatelet activity |
Use alternative agents |
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| Elvitegravir Vorapaxar 213 | Red: Avoid combination | Do not coadminister: Potential for increased levels of vorapaxar | Potential for increased risk of bleeding |
Avoid combination and use alternative antiplatelet agent |
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| Elvitegravir Ticagrelor 212 | Red: Avoid combination | Do not coadminister: Potential for increased levels of ticagrelor | Potential for increased risk of bleeding |
Avoid combination and use alternative antiplatelet agent. |
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| Elvitegravir Suvorexant 211 | Red: Avoid combination | Do not coadminister: Potential for increased levels of suvorexant | Potential for increased suvorexant adverse effects |
Use alternative agents |
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| Elvitegravir Salmeterol 210 | Red: Avoid combination | Do not coadminister: Potential for increased levels of salmeterol | Increased risk of cardiovascular adverse events (e.g. QT prolongation, palpitations, sinus tachycardia) |
Use alternative agents |
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| Elvitegravir Ranolazine 209 | Red: Avoid combination | Do not coadminister: Potential for increased levels of ranolazine | Potential for increased risk of ranolazine adverse effects |
Contraindicated. Use alternative agents. |
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| Elvitegravir Ivabradine 208 | Red: Avoid combination | Do not coadminister: Potential for increased levels of ivabradine | Potential for increased risk of ivabradine adverse effects |
Contraindicated. Use alternative agents. |
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| Elvitegravir Flibanserin 207 | Red: Avoid combination | Do not coadminister: Potential for increased levels of flibanserin | Potential for increased risk of flibanserin adverse effects |
Use alternative agents |
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| Elvitegravir Eplerenone 206 | Red: Avoid combination | Do not coadminister: Potential for increased levels of eplerenone | Potential for increased risk of eplerenone adverse effects |
Contraindicated. Use alternative agents. |
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| Elvitegravir Dofetilide 205 | Red: Avoid combination | Do not coadminister: Potential for increased levels of dofetilide | Potential for increased risk of dofetilide adverse effects |
Use alternative agents |
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| Elvitegravir Lumateperone 204 | Red: Avoid combination | Do not coadminister: potential toxicity | Potential for increased risk of lumateperone adverse effects |
Use alternative agents |
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| Elvitegravir Lurasidone 203 | Red: Avoid combination | Do not coadminister: potential toxicity | Potential serious or life-threatening reactions |
Contraindicated. Use alternative agents. |
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| Elvitegravir Triazolam 202 | Red: Avoid combination | Do not coadminister: Potential for increased levels of triazolam | Potential for increased triazolam effects (e.g. prolonged sedation, altered mental status, respiratory depression) |
Contraindicated. Use alternative agents. |
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| Elvitegravir Triamcinolone 201 | Red: Avoid combination | Do not coadminister: Potential for increased levels of triamcinolone | Potential for increased risk of adrenal insufficiency and Cushing's syndrome |
Do not coadminister if triamcinolone is used for local injection. |
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| Elvitegravir Simvastatin 200 | Red: Avoid combination | Do not coadminister: Potential for increased levels of simvastatin | Potential for increased simvastatin effects (e.g. myopathy, rhabdomyolysis) |
Contraindicated. Use alternative agents. |
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| Elvitegravir Simeprevir 199 | Red: Avoid combination | Do not coadminister: Potential for increased levels of simeprevir | Potential for increased simeprevir toxicity |
Use alternative agents |
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| Elvitegravir Silodosin 198 | Red: Avoid combination | Do not coadminister: Potential for increased levels of silodosin | Potential for increased silodosin adverse effects |
Contraindicated. Use alternative agents. |
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| Elvitegravir Pimozide 197 | Red: Avoid combination | Do not coadminister: Potential for increased levels of pimozide | Potential serious or life-threatening reactions such as cardiac arrhythmia. |
Contraindicated. Use alternative agents. |
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| Elvitegravir Mometasone 196 | Red: Avoid combination | Do not coadminister: Potential for increased levels of mometasone | Potential for increased risk of adrenal insufficiency and Cushing's syndrome |
Use alternative agents |
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| Elvitegravir Midazolam 195 | Red: Avoid combination | Do not coadminister: Potential for increased levels of midazolam | Potential for increased midazolam effects (e.g. prolonged sedation, altered mental status, respiratory depression) |
Co-administration of oral midazolam is contraindicated. Parenteral midazolam can be used with caution when given as a single dose in a closely monitored situation for procedural sedation. |
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| Elvitegravir Alprazolam 194 | Red: Avoid combination | Do not coadminister: Potential for increased levels of midazolam | Potential for increased alprazolam effects (e.g. sedation, altered mental status, respiratory depression) |
Coadministration of EVG with oral midazolam is contraindicated. Parenteral midazolam can be used with caution when given as a single dose in a closely monitored situation for procedural sedation. |
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| Elvitegravir Methylprednisolone 193 | Red: Avoid combination | Do not coadminister: Potential for increased levels of methylprednisolone | Potential for increased risk of adrenal insufficiency and Cushing's syndrome |
Do not coadminister if methylprednisolone being used for local injection. |
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| Elvitegravir Methylergonovine 192 | Red: Avoid combination | Do not coadminister: Potential for increased levels of methylergonovine | Potential for increased ergot effects (e.g. ergot toxicity, peripheral vasospasm, ischemia) |
Contraindicated. Use alternative agents. |
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| Elvitegravir HMG-CoA Reductase Inhibitors 191 | Red: Avoid combination | Do not coadminister: Potential for increased levels of lovastatin | Potential for increased lovastatin effects (e.g. myopathy, rhabdomyolysis) |
Contraindicated. Use alternative agents. |
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| Elvitegravir Fluticasone 190 | Red: Avoid combination | Do not coadminister: Potential for increased levels of fluticasone | Potential for increased risk of adrenal insufficiency and Cushing's syndrome |
Use alternative agents |
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| Elvitegravir Ergotamine 189 | Red: Avoid combination | Do not coadminister: Potential for increased levels of ergotamine | Potential for increased ergot effects (e.g. ergot toxicity, peripheral vasospasm, ischemia) |
Contraindicated. Use alternative agents. |
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| Elvitegravir Dihydroergotamine 188 | Red: Avoid combination | Do not coadminister: Potential for increased levels of dihydroergotamine | Potential for increased ergot effects (e.g. ergot toxicity, peripheral vasospasm, ischemia) |
Contraindicated. Use alternative agents. |
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| Elvitegravir EBR/GZR 187 | Red: Avoid combination | Do not coadminister: Potential for increased levels of antivirals | Potential for increased AUC of HCV agents |
No significant change |
Elbasvir Cmax increased 91%, AUC increased 118%; Grazoprevir Cmax increased 359%, AUC increased436% |
Use alternative agents |
|
| Elvitegravir Dasabuvir + Ombitasvir / Paritaprevir / Ritonavir 186 | Red: Avoid combination | Do not coadminister: Potential for increased levels of antivirals | Potential for increased AUC of HCV agents |
Use alternative agents |
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| Elvitegravir Alfuzosin 185 | Red: Avoid combination | Do not coadminister: Potential for increased levels of alfuzosin | Potential for increased alfuzosin adverse effects (e.g. hypotension) |
Contraindicated. Use alternative agents. |
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| Elvitegravir Lomitapide 184 | Red: Avoid combination | Do not coadminister: Potential for increased level of lomitapide | Potential for increased risk of elevated transaminases |
Contraindicated. Use alternative agents. |
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| Elvitegravir Avanafil 183 | Red: Avoid combination | Do not coadminister: Potential for increased level of avanafil | Potential for increased risk avanafil adverse effects |
Contraindicated. Use alternative agents. |
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| Elvitegravir Dapagliflozin / Saxagliptin 182 | Red: Avoid combination | Do not coadminister: Increased levels of saxagliptin | Potential for increased saxagliptin adverse effects |
Not reported |
saxagliptin 5 mg | Not reported |
Use alternative agents |
| Elvitegravir G/P 181 | Green: Administer standard doses | Administer standard doses | Potential increase in GLEC / PIB toxicity |
AUC increased 47% |
Glecaprevir AUC increased 3 fold; PIB AUC increased 57% |

