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First experience of using casirivimab/imdevimab in COVID-19 in the Russian Federation.
Infektsionnye Bolezni ; 20(3):129-132, 2022.
Article in Russian | EMBASE | ID: covidwho-2228223
ABSTRACT
The lack of effective etiotropic therapy is a serious challenge in the treatment of patients with COVID-19. The recent emergence of a new class of medications neutralizing monoclonal antibodies against the SARS-CoV-2 spike protein allows to partially solve this problem. This article presents a clinical case of a patient with an increased risk of COVID-19 complications (paroxysmal atrial fibrillation, atherogenic dyslipidemia, impaired carbohydrate tolerance) who was treated with 600 mg casirivimab and 600 mg imdevimab by intravenous infusion. A significant improvement in the patient's well-being was noted within the first 24 hours normalization of body temperature, stool, reduction of weakness, disappearance of arthralgia and myalgia. After 48 hours, a negative test result for SARS-CoV-2 RNA was obtained, which altogether made it possible to state the recovery. There were no adverse events during and after therapy. The casirivimab and imdevimab monoclonal antibody combination may be considered as a promising etiotropic treatment for COVID-19. Copyright © 2022, Dynasty Publishing House.
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Full text: Available Collection: Databases of international organizations Database: EMBASE Type of study: Prognostic study Language: Russian Journal: Infektsionnye Bolezni Year: 2022 Document Type: Article

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Full text: Available Collection: Databases of international organizations Database: EMBASE Type of study: Prognostic study Language: Russian Journal: Infektsionnye Bolezni Year: 2022 Document Type: Article