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Drugs.com FDA MedWatch Alerts
Original article

FAERS Receives Increased Reports of Allergic/Hypersensitivity Reactions with One Lot of Immune Globulin Intravenous (IGIV)

RegulatoryImmune Globulin Intravenous (IGIV)Negative
AI Analysis

Summary

The FDA's FAERS system has received increased reports of allergic and hypersensitivity reactions following infusion of a specific lot of Immune Globulin Intravenous (IGIV). The alert was issued to healthcare professionals and consumers on October 6, 2026.

Outcome Details

Increased adverse event reports of allergic/hypersensitivity reactions associated with a specific lot

Importance:5/10
Sentiment:
-0.70
safety alertadverse eventsFAERSallergic reactionproduct safety

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Published by Drugs.com FDA MedWatch Alerts on October 6, 2026 5:40 PM

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