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FDA Approves First-Ever Treatment for Severe Frostbite

Aurlumyn aims to significantly reduce the risk of amputation for frostbite patients.

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The drug was approved for sever cases of frostbite to reduce the risk of finger or toe amputation.
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Overview

  • The U.S. Food and Drug Administration (FDA) has approved Aurlumyn, the first-ever treatment for severe frostbite in adults, aimed at reducing the risk of finger or toe amputation.
  • Aurlumyn, also known as iloprost, is an injectable vasodilator that opens blood vessels and prevents blood clots, initially approved in 2004 for pulmonary arterial hypertension.
  • In a controlled trial, Aurlumyn demonstrated a significant reduction in the need for amputation among severe frostbite patients compared to other treatments.
  • Common side effects of Aurlumyn include headache, flushing, heart palpitations, fast heart rate, nausea, vomiting, dizziness, and hypotension.
  • Experts emphasize the importance of frostbite prevention through proper clothing, equipment, and training for cold-weather activities.