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Aduhelm Adverse Event Reports Come In, Another Potential Hurdle To Uptake

 
• By Jessica Merrill

One patient treated with Aduhelm died who was diagnosed with cerebral edema thought to be ARIA-E, a known risk, Biogen confirmed.

caution tape
Aduhelm early adverse events reports could lead to more caution around prescribing. • Source: Alamy

Biogen, Inc.'s first-in-class beta-amyloid antibody therapy Aduhelm (aducanumab) for Alzheimer's disease has gotten off to a rocky commercial start and initial adverse event reports could add to physician caution about prescribing the medicine.

One death in a patient treated with Aduhelm was reported to the US Food and Drug Administration's Adverse Event Reporting System (FAERS), which is updated quarterly

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