FDA approves Xocova for COVID-19 postexposure prophylaxis

FDA approves Xocova for COVID-19 postexposure prophylaxis

Publication date: Jun 10, 2026

The most common adverse events included headache, diarrhea, and cough, which occurred in 1% in the Xocova group and at a greater frequency than in the placebo group. This article has been reviewed according to Science X’s editorial process and policies . “The PEP strategy has the potential to benefit anyone who does not want to get COVID-19. All rights reserved.

Concepts Keywords
Coronavirus Approval
Fda Approved
Food Covid
Headache Day
Virginia Fda
Included
Mg
Oral
Pep
Placebo
Postexposure
Prophylaxis
Trial
Xocova

Semantics

Type Source Name
disease MESH cough
disease MESH diarrhea
disease MESH headache
disease MESH COVID-19
disease MESH included

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