Does DENOSUMAB Cause Condition aggravated? 469 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 469 reports of Condition aggravated have been filed in association with DENOSUMAB (Bilprevda). This represents 0.3% of all adverse event reports for DENOSUMAB.
469
Reports of Condition aggravated with DENOSUMAB
0.3%
of all DENOSUMAB reports
43
Deaths
95
Hospitalizations
How Dangerous Is Condition aggravated From DENOSUMAB?
Of the 469 reports, 43 (9.2%) resulted in death, 95 (20.3%) required hospitalization, and 14 (3.0%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DENOSUMAB. However, 469 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which DENOSUMAB Alternatives Have Lower Condition aggravated Risk?
DENOSUMAB vs DEOXYCHOLIC ACID
DENOSUMAB vs DEPAKINE CHRONO
DENOSUMAB vs DEPAKOTE
DENOSUMAB vs DEPO-PROVERA
DENOSUMAB vs DERMATOPHAGOIDES FARINAE