# Remdesivir: Real-World Effectiveness and Safety in Individuals Hospitalized for Non-COVID Reasons and Non-Hospitalized High-Risk Patients During the Omicron Era in Greece

**Authors:** Nikos Pantazis, Spyridon Kontos, Evmorfia Pechlivanidou, Nikolaos V. Sipsas, Diamantis Kofteridis, Periklis Panagopoulos, Vassiliki Rapti, Symeon Metallidis, Karolina Akinosoglou, Dimitra Kavatha, Haralampos Milionis, Ioannis Kalomenidis, Ioannis Katsarolis, Vasiliki E. Georgakopoulou, Vasileios Petrakis, Garyfallia Poulakou, Olga Tsachouridou, Markos Marangos, Anastasia Antoniadou, Eleni Polyzou, Eleni Papantoniou, Pinelopi Kazakou, Eirini Christaki, Theofani Rimpa, Sotirios P. Karagiannis, Giota Touloumi

PMC · DOI: 10.3390/microorganisms14020441 · Microorganisms · 2026-02-12

## TL;DR

This study examines remdesivir's effectiveness and safety in hospitalized non-COVID patients and high-risk outpatients during the Omicron era in Greece.

## Contribution

The study provides real-world evidence on remdesivir use in non-standard patient groups during the Omicron wave.

## Key findings

- Remdesivir was effective and safe in high-risk outpatients with no COVID-19-related deaths.
- Hospitalized incidental cases showed higher clinical deterioration and mortality rates.
- Adverse events were mild and more common in hospitalized patients.

## Abstract

Remdesivir is recommended for hospitalized patients with severe COVID-19 and for those at high risk of progression. Real-world Omicron-era data on incidental COVID-19 and high-risk outpatients remain limited. We conducted a multicenter retrospective cohort study (ReEs-COVID19) in Greece (June–December 2022) including adults with PCR-confirmed SARS-CoV-2 infection who received remdesivir. Hospitalized patients with incidental COVID-19 (Group A, n = 138) and high-risk outpatients (Group B, n = 312) were analysed. Outcomes included clinical deterioration, mortality, and adverse events. Group A patients were older with more comorbidities. Remdesivir was initiated earlier in Group A (median 1 vs. 2 days) but with a more heterogeneous duration (48.9% vs. 97.8% in Group B, which received the standard 3-day regimen). Clinical deterioration due to COVID-19 occurred in 5.8% vs. 0.6%, and 30-day mortality was 18.1% (25/138) in Group A, including 10 COVID-19-related deaths (7.2%). Group B had two deaths (0.6%), none COVID-19-related. Adverse events were uncommon, with mild kidney injury in 3.6% of Group A and hepatotoxicity in 2.2% vs. 0.3%. In high-risk outpatients, the ReEs-COVID19 study confirmed the effectiveness and safety of remdesivir’s profile. Among incidental cases, two distinct disease patterns were identified, associated with different remdesivir regimens and highlighting the importance of comorbidities and the need for tailored clinical interventions.

## Linked entities

- **Chemicals:** remdesivir (PubChem CID 121304016)
- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}
- **Diseases:** dizziness (MESH:D004244), atrial fibrillation (MESH:D001281), COVID-19 (MESH:D000086382), gastrointestinal intolerance (MESH:D005767), idiopathic pulmonary fibrosis (MESH:D054990), Cardiovascular disease (MESH:D002318), infection (MESH:D007239), myocardial infarction (MESH:D009203), death (MESH:D003643), hypertension (MESH:D006973), Renal and hepatic abnormalities (MESH:D000014), hepatic and renal laboratory abnormalities (MESH:D007757), cardiorenal disease (MESH:D059347), nosocomial infections (MESH:D003428), Sepsis (MESH:D018805), HIV (MESH:D015658), coronary artery disease (MESH:D003324), anaemia (MESH:D000743), Liver function abnormalities (MESH:D056486), biliary pathology (MESH:D005598), Kidney Disease (MESH:D007674), heart failure (MESH:D006333), musculoskeletal complaints (MESH:D009140), thyroid dysfunction (MESH:D013959), obstructive sleep apnoea (MESH:D020181), chronic kidney disease (MESH:D051436), asthma (MESH:D001249), abdominal pain (MESH:D015746), cancer (MESH:D009369), lung pathology (MESH:D008171), diabetes (MESH:D003920), coronary heart disease (MESH:D003327), critical illness (MESH:D016638), metabolic disturbances (MESH:D024821), Chronic liver disease (MESH:D008107), Comorbidity (MESH:D004194), injuries (MESH:D014947), frailty (MESH:D000073496), myelodysplastic syndrome (MESH:D009190), stroke (MESH:D020521), AKI (MESH:D058186), COPD (MESH:D029424), obesity (MESH:D009765)
- **Chemicals:** hepatic enzyme (-), Remdesivir (MESH:C000606551), Oxygen (MESH:D010100)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Full text

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## Figures

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## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943158/full.md

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Source: https://tomesphere.com/paper/PMC12943158