Remdesivir, Fluvoxamine can assist in treating COVID-19 patients

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Photo by Olga Kononenko on Unsplash
Photo by Olga Kononenko on Unsplash

Prescription medications Remdesivir and Fluvoxamine can both play a role in treating people with COVID-19, according to two papers from international researchers. In the first, Canadian researchers performed a randomised controlled trial among hospitalised COVID-19 patients, comparing the results of patients given Remdesivir for 10 days with patients given a placebo. They say the drug has a "modest but significant" effect, reducing poor outcomes such as patients needing ventilation. In the second paper, researchers performed a meta-analysis with three randomised controlled trials looking at Fluvoxamine as an early intervention. They say the drug has a high probability of preventing hospitalisation if taken early in the course of a COVID-19 infection.

Media release

From: Canadian Medical Association Journal

Remdesivir for COVID-19 found to reduce need for mechanical ventilation: RCT

Remdesivir, when compared with standard of care for COVID-19, reduced the need for mechanical ventilation in hospitalized patients, according to a new randomized controlled trial published in CMAJ (Canadian Medical Association Journal), Canada's major medical journal.

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The study, Canadian Treatments for COVID-19 (CATCO), is a Canadian Institutes of Health Research–funded substudy of the global World Health Organization Solidarity trial examining the effects of various treatments for COVID-19. In the CATCO trial, which involved 52 Canadian hospitals, Canadian researchers studied the effect of remdesivir in hospitalized patients with COVID-19 between August 14, 2020, and April 1, 2021. There were 1282 patients included, with about half randomized to receive treatment with remdesivir and the rest to the control group receiving standard care. Evidence has been mixed on the effect of remdesivir, a repurposed antiviral medication, in people with COVID-19.

The Canadian trial, led by researchers at the University of British Columbia and Sunnybrook Health Sciences Centre, found that among patients not receiving mechanical ventilation at the start of the study, the need for mechanical ventilation arose for 8% of patients receiving remdesivir compared with 15% of those receiving standard of care. In addition, patients treated with remdesivir were able to come off oxygen and ventilators sooner than those receiving standard care.

"The benefit of treatment was most apparent for preventing the need for mechanical ventilation, suggesting probable added value for patients with less severe disease to avoid progression during hospital stay," writes Dr. Srinivas Murthy, University of British Columbia, with coauthors. "This may have important implications for patients and for health systems, particularly when ICU capacity, mechanical ventilation or oxygen are in limited supply."

The CATCO trial was able to collect more detailed data than some other countries, as well as engage patients across a range of ethnicities, which is particularly important for applications in other countries and in our multicultural society. The study is also the largest single-country trial of remdesivir reported to date.

These results add to the larger global trial around how remdesivir could be used in other countries.

"The findings of CATCO are also important and complementary to Solidarity as they help to address questions of generalizability of a large simple protocol carried out across a wide range of hospitals and health care systems from low-, middle- and high-income countries," the authors conclude.

"Remdesivir for the treatment of patients in hospital with COVID-19 in Canada: a randomized controlled trial" is published January 19, 2022.

Fluvoxamine for symptomatic outpatients with COVID-19

Fluvoxamine, a commonly used antidepressant with anti-inflammatory and antiviral properties, has been found to be effective in treating some patients with COVID-19. A new article in CMAJ (Canadian Medical Association Journal) provides important information for its use in outpatients.

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Fluvoxamine may prevent hospital admission in symptomatic adults with COVID-19
The Ontario Science Table states that fluvoxamine may be considered for mildly ill patients within 7 days of symptom onset.

Fluvoxamine for COVID-19 has not been studied in children and pregnant people
As most studies included unvaccinated adults, caution and obstetrical consultation are advised for pregnant patients. Fluvoxamine is not recommended for pediatric patients.

Fluvoxamine was generally well tolerated in the clinical trials
Patient-reported adverse events included mild headache and gastrointestinal symptoms.

Food and drug pharmacokinetic interactions can occur
Caffeine and warfarin can interact with fluvoxamine. Caffeine intake should be limited to one serving per day, and patients on warfarin should be monitored. Fluvoxamine can reduce the efficacy of clopidogrel, a particular risk for patients with a recent ischemic stroke or cardiac stenting.

Fluvoxamine use can result in adverse reactions
It can interact with other antidepressants. The list of interactions can be found in Appendix 1, at www.cmaj.ca/lookup/ doi/10.1503/cmaj.220011/tab-related-content.

"Fluvoxamine for symptomatic outpatients with COVID-19" is published January 19, 2022.

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Research Canadian Medical Association Journal, Web page Paper 1
Research Canadian Medical Association Journal, Web page Paper 2
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Canadian Medical Association Journal
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Organisation/s: Niagara Health, Canada (Paper 1), Division of General Internal Medicine and Geriatrics, Canada (Paper 2)
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