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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 failure? 107 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 107 reports of Device failure have been filed in association with DENOSUMAB (Bilprevda). This represents 0.1% of all adverse event reports for DENOSUMAB.

107
Reports of Device failure with DENOSUMAB
0.1%
of all DENOSUMAB reports
1
Deaths
10
Hospitalizations

How Dangerous Is Device failure From DENOSUMAB?

Of the 107 reports, 1 (0.9%) resulted in death, 10 (9.3%) required hospitalization, and 1 (0.9%) were considered life-threatening.

Is Device failure Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DENOSUMAB. However, 107 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 failure?

EPINEPHRINE (1,344) SOMATROPIN (1,141) PEGFILGRASTIM (829) TREPROSTINIL (713) BACLOFEN (691) BUDESONIDE\FORMOTEROL (686) ETANERCEPT (576) GOLIMUMAB (487) LEVONORGESTREL (332) ACLIDINIUM (304)

Which DENOSUMAB Alternatives Have Lower Device failure 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 failure Reports All Drugs Causing Device failure DENOSUMAB Demographics