Does DEVICE Cause Off label use? 443 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 443 reports of Off label use have been filed in association with DEVICE. This represents 3.5% of all adverse event reports for DEVICE.
443
Reports of Off label use with DEVICE
3.5%
of all DEVICE reports
22
Deaths
63
Hospitalizations
How Dangerous Is Off label use From DEVICE?
Of the 443 reports, 22 (5.0%) resulted in death, 63 (14.2%) required hospitalization, and 10 (2.3%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 443 reports have been filed with the FAERS database.
What Other Side Effects Does DEVICE Cause?
Blood glucose increased (2,114)
Device issue (1,417)
Product use issue (1,076)
Intercepted product preparation error (1,033)
Wrong technique in product usage process (935)
Device leakage (795)
Injection site pain (751)
Syringe issue (634)
Product quality issue (567)
Drug ineffective (488)
What Other Drugs Cause Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which DEVICE Alternatives Have Lower Off label use Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN