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Stromectol Ivermectin is a highly effective medication that has been proven to be effective in treating parasitic infections. It has been used to treat river blindness, which is caused by a parasitic worm that is transmitted by the bite of black flies. It has also been used to treat strongyloidiasis, which is caused by a roundworm that is found in the soil in tropical and subtropical regions. In addition to its use in treating parasitic infections, there is growing evidence that Stromectol Ivermectin may have potential as a treatment for COVID Several studies have found that the drug can reduce the replication of the virus in laboratory settings.
On January, the World Health Organization WHO made the first recommendations on the epidemiological surveillance of this new coronavirus. New potential candidates for the treatment of this disease have emerged. It does something similar with other proteins of the SV40 virus and the dengue virus. Therefore, the development of clinical protocols comparing it with other antivirals with alternate mechanisms of action is important and should be established as soon as possible. In the study by Patel et al.
Patients with severe pneumonia were receiving high-flow nasal oxygen, mechanical ventilation invasive or noninvasive, or extracorporeal membrane oxygenation. The cumulative rate of symptom resolution is the percentage of patients who experienced their first day free of symptoms. If you have no conflicts of interest, check No potential conflicts of interest in the box below. Findings In this randomized clinical trial that included patients, the duration of symptoms was not significantly different for patients who received a 5-day course of ivermectin compared with placebo median time to resolution of symptoms, 10 vs 12 days; hazard ratio for resolution of symptoms, 1. Importance Ivermectin is widely prescribed as a potential treatment for COVID despite uncertainty about its clinical benefit. Solicited adverse events and serious adverse events were also collected. The median time to resolution of symptoms was 10 days IQR, in the ivermectin group compared with 12 days IQR, in the placebo group hazard ratio for resolution of symptoms, 1. The most common serious adverse event was multiorgan failure, occurring in 4 patients 2 in each group. Conclusion and Relevance Among adults with mild COVID, a 5-day course of ivermectin, compared with placebo, did not significantly improve the time to resolution of symptoms.
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