Date of report: 27 Feb 2020
Reported case interaction between
Atazanavir and Naringin
Atazanavir and Naringin

Drugs suspected to be involved in the DDI
Drug A
Atazanavir
(Victim)
Daily Dose
300
(mg)
Dose adjustment performed
No
Administration Route
Oral
Start date
Unknown
End date
Unknown
Drug B
Naringin
(Perpetrator)
Daily Dose
Unknown
Dose adjustment performed
No
Administration Route
Oral
Start date
Unknown
End date
Unknown
Complete list of drugs taken by the patient
Antiretroviral treatment
Emtricitabine/Tenofovir-DF
Atazanavir (unboosted)
Complete list of all comedications taken by the patient, included that involved in the DDI
Naringin-copntaining CAM, sinetrol, fluoxetine, pseudoephedrine
Clinical case description
Gender
Female
Age
40
eGFR (mL/min)
>60
Liver function impairment
No
Description
Patient failing antiretroviral therapy with atazanavir plus tenofovir/emtricitabine (mean HIV RNA: 149 copies/mL). He referred that he had recently started using a naringin‐containing supplement, claimed to be a fat‐burning accelerator. TDM revealed suboptimal atazanavir concentration during concomitant treatment with naringin that increased after discontinuation (85 versus 719 ng/mL).
This case has been published by Cattaneo D, et al. in Obesity (Silver Spring). 2018
Aug;26(8):1251-1252.
Outcome
Loss of efficacy
Drug Interaction Probability Scale (DIPS)
Score
7 - Probable
Editorial Comment
Weight-loss drugs should be used with caution in HIV-infected patients treated with antiretroviral drugs because of the risk of virologic failure.
Naringin is a flavanone‐7‐O‐glycoside that inhibits the activity of carrier proteins (p‐glycoprotein and organic‐anion‐transporting polypeptide), ultimately resulting in impaired drug absorption (Shirasaka Y, Li Y, Shibue Y, et al. Concentration‐dependent effect of naringin on intestinal absorption of beta(1)‐adrenoceptor antagonist talinolol mediated by p‐glycoprotein and organic anion transporting polypeptide (OATP). Pharm Res 2009; 26: 560‐ 567.)