Potential ↑ fentanyl concentrations. Due to the risk of clinically significant toxicity including respiratory depression, coadministration is not recommended.
Potential ↑ fentanyl concentration via CYP3A4 inhibition by cobicistat.
Pharmacokinetic study with ritonavir: In a healthy volunteer study, a 67% reduction in clearance and 174% increase in AUC of fentanyl was observed when IV fentanyl was coadministered with ritonavir 900 mg/day. Monitor for respiratory and CNS depression.1002
Significant interactions between transdermal fentanyl and CYP3A4 inhibitors including itraconazole, fluconazole, clarithromycin and lopinavir/ritonavir have been reported, with consequences including opioid toxicity, respiratory depression and/or death. These cases are described in more detail below.
Clarithromycin: an 81 year old male with dementia, COPD, cervical spondylosis and spinal stenosis received H. pylori treatment with clarithromycin and metronidazole while on fentanyl 200 ug/hour. Thirty-six hours after the antibiotics were started, he was unresponsive to verbal and tactile stimuli and was treated with naloxone. He was subsequently stabilized on fentanyl 100 ug/hour.2799
Fluconazole: a 46 year old man with tonsillar cancer was on fentanyl 150 ug/hour for pain control. Three weeks later, fluconazole 50 mg daily was started for oral candidiasis. The patient died 3 days later; toxic fentanyl concentrations (approximately 6-fold greater than the upper therapeutic range) were noted.2788
Itraconazole: a 67 year old male with head and neck cancer was on fentanyl 50 ug/hour. He started treatment with itraconazole 200 mg BID for oropharyngeal candidiasis. Signs and symptoms of opioid toxicity were noted the next day, and he was eventually stablized on fentanyl 25 ug/hour.2797
Lopinavir/ritonavir: a 46 year old female on fentanyl 100 ug/hour received HIV post-exposure prophylaxis with lopinavir/ritonavir and zidovudine/lamivudine. Four days later she was very drowsy and needed frequent wakening. She was found unresponsive later that night.2800
The Evotaz product monograph recommends careful monitoring of therapeutic effect and adverse effects of fentanyl (including respiratory depression) with coadministration.2566
The Duragesic MAT (fentanyl) monograph states that concomitant use of transdermal fentanyl and CYP3A4 inhibitors is not recommended unless the patient is monitored closely for signs of respiratory depression. Monitoring should be done for an extended period of time, with fentanyl dose adjustments as required.2801
Due to the risk of clinically significant outcomes (including respiratory depression), coadministration of fentanyl with CYP3A4 inhibitors including cobicistat or ritonavir is not recommended.
Extensively metabolized by CYP3A4. Atazanavir inhibits CYP3A and UGT1A1 at clinically relevant concentrations. Atazanavir is a weak inhibitor of CYP2C8. Caution when unboosted atazanavir is coadministered with drugs that are 2C8 substrates with narrow therapeutic indices (e.g., paclitaxel, repaglinide); clinically significant interactions with 2C8 substrates are not expected when atazanavir is boosted with ritonavir.
Atazanavir does not inhibit CYP2C19 or CYP2E1 at clinically relevant concentrations.
Avoid concomitant administration with antacids, proton-pump inhibitors, or H2-blockers, as atazanavir absorption is significantly compromised.
Atazanavir is an inhibitor of CYP3A and UGT1A1. Atazanavir is a weak inhibitor of CYP2C8. With boosted atazanavir, ritonavir appears to induce CYP2C8 and offset inhibition by ATV.1463
Recommended Atazanavir and Ritonavir Dosage in Adults
Atazanavir Once Daily Dosage | Ritonavir Once Daily Dosage | |
Treatment-Naive Adult Patients | ||
recommended regimen | 300 mg | 100 mg |
unable to tolerate ritonavir | 400 mg | N/A |
in combination with efavirenz | 400 mg | 100 mg |
Treatment-Experienced Adult Patients | ||
recommended regimen | 300 mg | 100 mg |
in combination with both H2RA and tenofovir | 400 mg | 100 mg |
Recommended Dosage of Atazanavir and Ritonavir in Pregnant Patients
Atazanavir Once Daily Dosage | Ritonavir Once Daily Dosage | |
Treatment-Naive and Treatment-Experienced | ||
Recommended Regimen | 300 mg | 100 mg |
Treatment-Experienced During the Second or Third Trimester When Coadministered with either H2RA or Tenofovir | ||
In combination with either H2RA or tenofovir | 400 mg | 100 mg |
Atazanavir/cobocistat: 1 tablet (atazanavir 300mg, cobicistat 150mg) once daily with food.
Steady-state atazanavir concentrations in HIV-positive subjects after 400 mg QD administration with food:
Cmax 3152 ng/mL, Cmin 273 ng/mL, AUC 22262 ng.h/mL
Atazanavir plasma concentrations after 300/100 mg ritonavir QD: Cmax 5233 ng/mL, Cmin 862 ng/mL, AUC 53761 ng.h/mL
Atazanavir administered in a fixed-dose tablet (300 mg atazanavir/150 mg cobicistat) demonstrated bioequivalence to coadministration of the individual components when given with a light meal in healthy adult subjects.2892
10 HIV positive patients on ATV 400mg daily switched to ATV 200mg BID, atazanavir kinetics assessed at baseline and after 10 days of BID regimen. Atazanavir 200mg BID led to higher plasma Ctrough, lower Cmax and similar AUC compared to standard ATV 400mg daily dose.2910 2895
Mean plasma levels | ATV 400 mg daily (Baseline) | ATV 200 mg BID | Mean plasma GM ratios (ATV 200 BID:ATV 400 mg QD) |
Ctrough (ng/ml) | 138 | 305 | 2.19 |
Cmax (ng/ml) | 2786 | 1314 | 0.48 |
AUC24h (ng.h/ml) | 20780 | 16904 | 0.8 |
Mean intracellular levels | ATV 400 mg daily (Baseline) | ATV 200 mg BID | Mean intracellular GM ratios (ATV 200 BID:ATV 400 mg QD) |
Ctrough (ng/ml) | 465 | 2.93 | |
Cmax (ng/ml) | 4058 | 1.27 | |
AUC24h (ng.h/ml) | 35958 | 1.51 |
Increased bilirubin levels with BID regimen not clinically important. Atazanavir accumulates within the cell to a slightly greater extent versus plasma.
Open label, prospective, single center study to investigate kinetics of lower dose ATV/r. 22 Thai HIV infected adult patients suppressed on ATV/r 300mg/100mg daily were changed to 200mg/100mg daily (7 pts were also on TDF).
Median | ATV/r 300/100mg at baseline | ATV/r 200mg/100mg at day 14 | p |
AUC 0-12hr (mg.h/L) | 65.4 | 35.5 | < 0.001 |
Cmax (mg/L) | 6.1 | 3.9 | < 0.001 |
Cmin (mg/L) | 1 | 0.5 | < 0.001 |
No patients had subtherapeutic levels (< 0.15mg/L).2896 Results of ATV/r 200/100mg daily in Thai subjects comparable to Caucasian population on standard dose.2896
In 29 HIV-infected patients receiving atazanavir-based therapy (14 unboosted, 15 boosted), median intracellular atazanavir Ctrough concentrations were higher for boosted vs. unboosted atazanavir, and intracellular concentrations were higher than median plasma Ctrough:
Median (+IQR) | Unboosted ATV | Boosted ATV | p |
Plasma Ctrough (ng/mL) | 132 (111-184) | 543 (393-1081) | |
Intracellular Ctrough (ng/mL) | 328 (168-440) | 1032 (819-3091) | 0.001 |
p=0.001 | p=0.005 |
In 416 HIV-positive subjects on atazanavir-based regimens, routine atazanavir Ctrough was not significantly different between smokers (n=246) and non-/ex-smokers (n=170)2903. In healthy subjects taking either atazanavir or atazanavir/ritonavir, moderate tobacco use (up to 10 cigarettes per day) was not associated with a significant difference in atazanavir pharmacokinetics.2898
In 18 HIV-infected women on ≥ 6 months of cART (tenofovir, emtricitabine, atazanavir, and ritonavir) with plasma viral loads < 50 copies/mL, blood and cervicovaginal samples were collected twice weekly for three weeks following menses. The ratio of cervicovaginal to plasma drug concentrations (geometric mean) was 11.6 for emtricitabine (CI 8.1-16.6), 3.18 for tenofovir (CI 1.94-5.21), 2.59 for atazanavir (CI 1.81-3.71), and 1.52 for ritonavir (CI 1.04-2.23). HIV-1 RNA was detected in 14 cervicovaginal samples (13.7%, CI 7.7%-24.1%) from 8 (44%) women; all virus-positive samples had virus loads < 500 copies/10 mL CVL.2899
Atazanavir total and unbound concentrations were measured in HIV-positive subjects with compensated cirrhosis (n=8, median MELD 11, Child score A, n=7 or B n=1) and HIV-positive subjects without hepatic disease (n=3). In patients with compensated cirrhosis, total and unbound atazanavir concentrations were similar to controls and historical data.2900
A case report of a 37 year old HIV/HCV coinfected male (60 kg) who ingested 8700 mg atazanavir without ritonavir; last ritonavir 100 mg dose was taken ~24 hours prior to overdose. Transient elevation in total bilirubin and Scr and asymptomatic increases in PR and QTc intervals were observed at 24-48 hours post-overdose; values returned to baseline at one-month follow-up. Atazanavir plasma concentrations were 5400 ng/mL and 594 ng/mL at 22 and 62 hours post-overdose.2901
Atazanavir/cobicistat: In a trial where HIV-infected subjects (n=22) were instructed to take atazanavir 300 mg with cobicistat 150 mg once daily with food, the steady-state atazanavir Cmax, AUCtau and Ctau (mean ± SD) values were 3.9 ± 1.9 μg/ml, 46.1 ± 26.2 μg•hr/ml and 0.80 ± 0.72 μg/ml, respectively. Steady-state cobicistat Cmax, AUCtau and Ctau (mean ± SD) values were 1.5 ± 0.5 μg/ml, 11.1 ± 4.5 μg•hr/ml and 0.05 ± 0.07 μg/ml, respectively (n=22).2889
Substrate of CYP3A4. Intestinal p-gp plays a role in the absorption of oral fentanyl.
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