Does HUMAN IMMUNOGLOBULIN G\HYALURONIDASE Cause Device malfunction? 16 Reports in FDA Database

According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Device malfunction have been filed in association with HUMAN IMMUNOGLOBULIN G\HYALURONIDASE. This represents 0.6% of all adverse event reports for HUMAN IMMUNOGLOBULIN G\HYALURONIDASE.

How Dangerous Is Device malfunction From HUMAN IMMUNOGLOBULIN G\HYALURONIDASE?

Of the 16 reports, 8 (50.0%) required hospitalization.

Is Device malfunction Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for HUMAN IMMUNOGLOBULIN G\HYALURONIDASE. However, 16 reports have been filed with the FAERS database.

What Other Side Effects Does HUMAN IMMUNOGLOBULIN G\HYALURONIDASE Cause?