Evidence map›Paper›PMID 36536192›Full record

ArticleJournal of medical toxicology : official journal of the American College of Medical Toxicology2023

Tacrolimus Drug-Drug Interaction with Nirmatrelvir/Ritonavir (Paxlovid™) Managed with Phenytoin.

Morganne Sindelar, Daniel McCabe, Elisabeth Carroll

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in Journal of medical toxicology : official journal of the American College of Medical Toxicology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
6.7field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 32 citations in OpenAlex.

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  17. Response to Comment on "Tacrolimus Drug-Drug Interaction with Nirmatrelvir/Ritonavir (Paxlovid™) Managed with Phenytoin".Journal of medical toxicology : official journal of the American College of Medical Toxicology · 2023
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  18. Comment on "Tacrolimus Drug-Drug Interaction with Nirmatrelvir/Ritonavir (Paxlovid™) Managed with Phenytoin".Journal of medical toxicology : official journal of the American College of Medical Toxicology · 2023
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  19. Tacrolimus toxicity due to enzyme inhibition from ritonavir.The American journal of emergency medicine · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Morganne SindelarUniversity of Iowa Hospitals and Clinics, 200 Hawkins Drive, IA, 52242, Iowa City, USA. morganne-sindelar@uiowa.edu.ORCID 0000-0001-7136-0116
Daniel McCabeUniversity of Iowa Hospitals and Clinics, 200 Hawkins Drive, IA, 52242, Iowa City, USA.
Elisabeth CarrollUniversity of Iowa Hospitals and Clinics, 200 Hawkins Drive, IA, 52242, Iowa City, USA.
University of Iowa Hospitals and Clinics · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2 or COVID-19) pandemic has had a significant impact on communities and health systems. The Federal Drug Administration (FDA) authorized Pfizer's nirmatrelvir/ritonavir (Paxlovid™) through an EUA for the treatment of mild to moderate cases of COVID-19 at high risk for progression to severe disease. Patients with a history of transplant who test positive for COVID-19 are considered high risk because of their immunosuppression and are therefore candidates for nirmatrelvir/ritonavir. CASE REPORT: This is a case of a 67-year-old female with a past medical history of orthotopic heart transplant who received tacrolimus as part of her immunosuppressive regimen. She originally presented with complaints of dyspnea and cough for several days in the setting of COVID-19. The patient was started on nirmatrelvir/ritonavir due to her high risk for progression to severe disease. Four days after starting nirmatrelvir/ritonavir, she presented to the ED for slowed speech, fatigue, weakness, and loss of appetite. Upon admission she was found to have a supratherapeutic tacrolimus level of 176.4 ng/mL and an acute kidney injury. In this case, phenytoin was used as a CYP3A4 inducer to quickly decrease the tacrolimus level to within therapeutic range.

conclusionThis case highlights the strong and important drug-drug interaction between tacrolimus and nirmatrelvir/ritonavir leading to toxic levels of tacrolimus. It also demonstrates the utility and effectiveness of phenytoin as a "rescue" medication for tacrolimus toxicity.

Indexed as

COVID-19TacrolimusAgedCOVID-19 Drug TreatmentDrug InteractionsFemaleHumansLactamsLeucineNitrilesPhenytoinProlineRitonavirSARS-CoV-2LactamsLeucinenirmatrelvirNitrilesPhenytoinProlineRitonavirTacrolimusDrug-drug-interactionnirmatrelvir/ritonavirPaxlovid™PhenytoinTacrolimus toxicity

Identifiers

PMID36536192
PMCPMC9762866
OpenAlexW4311940484

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.