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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 DENOSUMAB Cause Device related sepsis? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Device related sepsis have been filed in association with DENOSUMAB (Bilprevda). This represents 0.0% of all adverse event reports for DENOSUMAB.

6
Reports of Device related sepsis with DENOSUMAB
0.0%
of all DENOSUMAB reports
4
Deaths
6
Hospitalizations

How Dangerous Is Device related sepsis From DENOSUMAB?

Of the 6 reports, 4 (66.7%) resulted in death, 6 (100.0%) required hospitalization, and 1 (16.7%) were considered life-threatening.

Is Device related sepsis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DENOSUMAB. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does DENOSUMAB Cause?

Off label use (34,612) Death (16,545) Osteonecrosis of jaw (8,438) Arthralgia (5,890) Pain in extremity (4,541) Back pain (4,465) Pain (4,102) Product storage error (3,621) Fall (3,322) Fatigue (3,009)

What Other Drugs Cause Device related sepsis?

TEDUGLUTIDE (226) TREPROSTINIL (225) CYCLOPHOSPHAMIDE (130) RITUXIMAB (113) EPOPROSTENOL (89) CYCLOSPORINE (82) METHYLPREDNISOLONE (82) BORTEZOMIB (79) MACITENTAN (55) DEXAMETHASONE (53)

Which DENOSUMAB Alternatives Have Lower Device related sepsis Risk?

DENOSUMAB vs DEOXYCHOLIC ACID DENOSUMAB vs DEPAKINE CHRONO DENOSUMAB vs DEPAKOTE DENOSUMAB vs DEPO-PROVERA DENOSUMAB vs DERMATOPHAGOIDES FARINAE

Related Pages

DENOSUMAB Full Profile All Device related sepsis Reports All Drugs Causing Device related sepsis DENOSUMAB Demographics