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Early Onset Favipiravir Saves Lives

Karatas et al., Research Square, doi:10.21203/rs.3.rs-142868/v1
Jan 2021  
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Retrospective 180 hospitalized patients showing lower mortality when Favipiravir is given earlier. 17% of patients given Favipiravir within 3 days died, compared to 38% when given after 3 days.
Potential risks of favipiravir include the creation of dangerous variants, and mutagenicity, carcinogenicity, teratogenicity, and embryotoxicity1-5.
Karatas et al., 14 Jan 2021, preprint, 5 authors.
This PaperFavipiravirAll
Early Onset Favipiravir Saves Lives
Ercan Karatas, Lacin Aksoy, Pinar Elbir Kilic, Arzu Dogru, Ersin Ozaslan
doi:10.21203/rs.3.rs-142868/v1
Background Favipiravir, an antiviral recommended for use in patients with tachypnea (respiratory rate 30 / min) in COVID-19 pneumonia, with SpO2 level below 90% in room air and with bilateral diffuse pneumonia on chest X-ray or tomography, or patients with treatment-resistant fever, is a new type of RNA-dependent RNA polymerase (RdRp) inhibitor. After the administration of Favipiravir, it contributed signi cantly to reducing mortality in patients with severe COVID-19 positive disease. We performed this study to determine the start time in Favipiravir's covid pneumonia. Material and Method: We evaluated the effect of a total of 5 days of oral treatment as a 2 × 1600 mg loading dose and a 2 × 600 mg maintenance dose of Favipiravir added to the standard COVID-19 treatment received by patients with laboratory-radiology-clinical ndings who have advanced or severe COVID 19 pneumonia. Results 180 patients hospitalized at Tuzla State Hospital and given Favipiravir treatment between 20/3/2020 and 30/5/2020 were examined. As of hospitalization, 17 of 101 patients (17%) who were given Favipiravir treatment in ≤ 3 days died, 30 of 79 patients (38%) who were given Favipiravir treatment for in > 3 days died (p:0.002). 33 of 47 patients (70%) who died were > 65 years old. Only 5 of the 47 (11%) patients who died had no comorbid disease. 35 had two or more comorbid diseases. Conclusion
Competing interests The authors declare that they have no competing interests Authors' contributions EK,LA conceived this review; EK,LA,EÖ performed the literature review and wrote the paper; PEK,AD helped with the review and writing of the paper; all authors read and approved the nal manuscript. Authors' information Ercan Karatas
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DOI record: { "DOI": "10.21203/rs.3.rs-142868/v1", "URL": "http://dx.doi.org/10.21203/rs.3.rs-142868/v1", "abstract": "<jats:title>Abstract</jats:title>\n <jats:p>Background\n Favipiravir, an antiviral recommended for use in patients with tachypnea (respiratory rate 30 / min) in COVID-19 pneumonia, with SpO2 level below 90% in room air and with bilateral diffuse pneumonia on chest X-ray or tomography, or patients with treatment-resistant fever, is a new type of RNA-dependent RNA polymerase (RdRp) inhibitor. After the administration of Favipiravir, it contributed significantly to reducing mortality in patients with severe COVID-19 positive disease. We performed this study to determine the start time in Favipiravir's covid pneumonia.\nMaterial and Method:\n We evaluated the effect of a total of 5 days of oral treatment as a 2 × 1600 mg loading dose and a 2 × 600 mg maintenance dose of Favipiravir added to the standard COVID-19 treatment received by patients with laboratory-radiology-clinical findings who have advanced or severe COVID 19 pneumonia.\nResults\n 180 patients hospitalized at Tuzla State Hospital and given Favipiravir treatment between 20/3/2020 and 30/5/2020 were examined. As of hospitalization, 17 of 101 patients (17%) who were given Favipiravir treatment in ≤ 3 days died, 30 of 79 patients (38%) who were given Favipiravir treatment for in &gt; 3 days died (p:0.002). 33 of 47 patients (70%) who died were &gt; 65 years old. Only 5 of the 47 (11%) patients who died had no comorbid disease. 35 had two or more comorbid diseases.\nConclusion\n Patients with radiological findings indicating that COVID-19 will be severe and laboratory findings at the time of the first 3 days should be initiated with an effective dose of Favipiravir treatment without waiting for the clinical worsening.</jats:p>", "accepted": { "date-parts": [ [ 2021, 1, 7 ] ] }, "author": [ { "ORCID": "http://orcid.org/0000-0002-3133-4199", "affiliation": [ { "name": "Turkiye Cumhuriyeti Saglik Bakanligi" } ], "authenticated-orcid": false, "family": "KARATAS", "given": "Ercan", "sequence": "first" }, { "affiliation": [ { "name": "Marmara Universitesi Tip Fakultesi, Family Practicies" } ], "family": "Aksoy", "given": "Lacin", "sequence": "additional" }, { "affiliation": [ { "name": "İstanbul Tuzla State Hospital" } ], "family": "Kilic", "given": "Pinar Elbir", "sequence": "additional" }, { "affiliation": [ { "name": "Tuzla State Hospital: Tuzla Devlet Hastanesi" } ], "family": "Dogru", "given": "Arzu", "sequence": "additional" }, { "affiliation": [ { "name": "Acibadem Hospitals Group: Acibadem Saglik Grubu" } ], "family": "Ozaslan", "given": "Ersin", "sequence": "additional" } ], "container-title": [], "content-domain": { "crossmark-restriction": false, "domain": [] }, "created": { "date-parts": [ [ 2021, 1, 15 ] ], "date-time": "2021-01-15T00:44:19Z", "timestamp": 1610671459000 }, "deposited": { "date-parts": [ [ 2022, 7, 29 ] ], "date-time": "2022-07-29T00:55:12Z", "timestamp": 1659056112000 }, "group-title": "In Review", "indexed": { "date-parts": [ [ 2024, 3, 3 ] ], "date-time": "2024-03-03T12:35:06Z", "timestamp": 1709469306410 }, "institution": [ { "name": "Research Square" } ], "is-referenced-by-count": 4, "issued": { "date-parts": [ [ 2021, 1, 13 ] ] }, "license": [ { "URL": "https://creativecommons.org/licenses/by/4.0/", "content-version": "unspecified", "delay-in-days": 0, "start": { "date-parts": [ [ 2021, 1, 13 ] ], "date-time": "2021-01-13T00:00:00Z", "timestamp": 1610496000000 } } ], "link": [ { "URL": "https://www.researchsquare.com/article/rs-142868/v1", "content-type": "text/html", "content-version": "vor", "intended-application": "text-mining" }, { "URL": "https://www.researchsquare.com/article/rs-142868/v1.html", "content-type": "unspecified", "content-version": "vor", "intended-application": "similarity-checking" } ], "member": "8761", "original-title": [], "posted": { "date-parts": [ [ 2021, 1, 13 ] ] }, "prefix": "10.21203", "published": { "date-parts": [ [ 2021, 1, 13 ] ] }, "publisher": "Research Square Platform LLC", "reference-count": 0, "references-count": 0, "relation": { "is-preprint-of": [ { "asserted-by": "subject", "id": "10.3947/ic.2020.0149", "id-type": "doi" } ] }, "resource": { "primary": { "URL": "https://www.researchsquare.com/article/rs-142868/v1" } }, "score": 1, "short-title": [], "source": "Crossref", "subject": [], "subtitle": [], "subtype": "preprint", "title": "Early Onset Favipiravir Saves Lives", "type": "posted-content" }
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