BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RELIZORB

    MDR report key: 25303317 · Received May 27, 2026

    Report

    Report Number
    MW5188657
    Event Type
    Injury
    Date Received
    May 27, 2026
    Date of Event
    May 10, 2026
    Report Date
    May 21, 2026
    Manufacturer
    ALCRESTA THERAPEUTICS, INC.
    Product Code
    PLQ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    PHARMACIST
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    PATIENT WAS HOSPITALIZED FOR HIGH BLOOD SUGAR FROM MAY 10-12 AND WAS DIAGNOSED WITH DIABETES. THEY ARE STILL TAKING RELIZORB WITH NO CHANGES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    248090 RELIZORB ENZYME PACKED CARTRIDGE PLQ ALCRESTA THERAPEUTICS, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 55 YR Male Hospitalization