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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does HYALURONIDASE RECOMBINANT HUMAN Cause Sepsis? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Sepsis have been filed in association with HYALURONIDASE RECOMBINANT HUMAN. This represents 10.6% of all adverse event reports for HYALURONIDASE RECOMBINANT HUMAN.

5
Reports of Sepsis with HYALURONIDASE RECOMBINANT HUMAN
10.6%
of all HYALURONIDASE RECOMBINANT HUMAN reports
1
Deaths
5
Hospitalizations

How Dangerous Is Sepsis From HYALURONIDASE RECOMBINANT HUMAN?

Of the 5 reports, 1 (20.0%) resulted in death, 5 (100.0%) required hospitalization, and 1 (20.0%) were considered life-threatening.

Is Sepsis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for HYALURONIDASE RECOMBINANT HUMAN. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does HYALURONIDASE RECOMBINANT HUMAN Cause?

Dehydration (7) Neutropenia (6) Atrial fibrillation (5)

What Other Drugs Cause Sepsis?

RITUXIMAB (4,043) CYCLOPHOSPHAMIDE (4,041) METHOTREXATE (3,933) ADALIMUMAB (3,169) DEXAMETHASONE (3,150) LENALIDOMIDE (2,956) VINCRISTINE (2,791) DOXORUBICIN (2,740) PREDNISONE (2,634) PREDNISOLONE (2,281)

Related Pages

HYALURONIDASE RECOMBINANT HUMAN Full Profile All Sepsis Reports All Drugs Causing Sepsis HYALURONIDASE RECOMBINANT HUMAN Demographics