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Potential pharmacokinetic interactions with concurrent use of herbal medicines and a ritonavir-boosted COVID-19 protease inhibitor in low and middle-income countries

Affiliation
Epidemic Intelligence Service ,Centers for Disease Control and Prevention ,Atlanta ,GA ,United States
Smith, Dallas J.;
Affiliation
School of Pharmaceutical Sciences ,Southern Medical University ,Guangzhou ,China
Bi, Huichang;
Affiliation
Centre of Excellence for Pharmaceutical Sciences (Pharmacen™) ,Faculty of Health Sciences ,North-West University ,Potchefstroom ,South Africa
Hamman, Josias;
Affiliation
Department of Pharmaceutical Sciences, School of Pharmacy, University of Pittsburgh ,Pittsburgh ,PA ,United States
Ma, Xiaochao;
Affiliation
Health and Environmental Sciences Institute ,Washington ,DC ,United States
Mitchell, Constance;
Affiliation
Department of Pharmacy, Kamuzu University of Health Sciences ,Blantyre ,Malawi
Nyirenda, Kumbukani;
Affiliation
Research Unit for Safety of Herbs and Drugs ,University of Zimbabwe ,Harare ,Zimbabwe
Monera-Penduka, Tsitsi;
Affiliation
United States Pharmacopeia ,Rockville ,MD ,United States
Oketch-Rabah, Hellen;
Affiliation
Department of Pharmaceutical Sciences, College of Pharmacy and Pharmaceutical Sciences, Washington State University ,Spokane ,WA ,United States
Paine, Mary F.;
Affiliation
Health and Environmental Sciences Institute ,Washington ,DC ,United States
Pettit, Syril;
Affiliation
DSI/NWU Preclinical Drug Development Platform ,Faculty of Health Sciences ,North-West University ,Potchefstroom ,South Africa
Pheiffer, Wihan;
Affiliation
Department of Pharmaceutical Sciences, College of Pharmacy, Oregon State University ,Corvallis ,OR ,United States
Van Breemen, Richard B.;
Affiliation
Health and Environmental Sciences Institute ,Washington ,DC ,United States
Embry, Michelle

The COVID-19 pandemic sparked the development of novel anti-viral drugs that have shown to be effective in reducing both fatality and hospitalization rates in patients with elevated risk for COVID-19 related morbidity or mortality. Currently, nirmatrelvir/ritonavir (Paxlovid™) fixed-dose combination is recommended by the World Health Organization for treatment of COVID-19. The ritonavir component is an inhibitor of cytochrome P450 (CYP) 3A, which is used in this combination to achieve needed therapeutic concentrations of nirmatrelvir. Because of the critical pharmacokinetic effect of this mechanism of action for Paxlovid™, co-administration with needed medications that inhibit or induce CYP3A is contraindicated, reflecting concern for interactions with the potential to alter the efficacy or safety of co-administered drugs that are also metabolized by CYP3A. Some herbal medicines are known to interact with drug metabolizing enzymes and transporters, including but not limited to inhibition or induction of CYP3A and P-glycoprotein. As access to these COVID-19 medications has increased in low- and middle-income countries (LMICs), understanding the potential for herb-drug interactions within these regions is important. Many studies have evaluated the utility of herbal medicines for COVID-19 treatments, yet information on potential herb-drug interactions involving Paxlovid™, specifically with herbal medicines commonly used in LMICs, is lacking. This review presents data on regionally-relevant herbal medicine use (particularly those promoted as treatments for COVID-19) and mechanism of action data on herbal medicines to highlight the potential for herbal medicine interaction Herb-drug interaction mediated by ritonavir-boosted antiviral protease inhibitors This work highlights potential areas for future experimental studies and data collection, identifies herbal medicines for inclusion in future listings of regionally diverse potential HDIs and underscores areas for LMIC-focused provider-patient communication. This overview is presented to support governments and health protection entities as they prepare for an increase of availability and use of Paxlovid™.

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License Holder: Copyright © 2023 Smith, Bi, Hamman, Ma, Mitchell, Nyirenda, Monera-Penduka, Oketch-Rabah, Paine, Pettit, Pheiffer, Van Breemen and Embry.

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