As of 4-5-22, the use of Sotrovimab- Monoclonal autobody infusion is no longer authorized by the FDA in the USA secondary to the Omicron BA.2 sub-variant.
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As of 4-5-22, the use of Sotrovimab- Monoclonal autobody infusion is no longer authorized by the FDA in the USA secondary to the Omicron BA.2 sub-variant.
"*" indicates required fields
