Does DEVICE Cause Product use issue? 1,076 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,076 reports of Product use issue have been filed in association with DEVICE. This represents 8.4% of all adverse event reports for DEVICE.
1,076
Reports of Product use issue with DEVICE
8.4%
of all DEVICE reports
5
Deaths
94
Hospitalizations
How Dangerous Is Product use issue From DEVICE?
Of the 1,076 reports, 5 (0.5%) resulted in death, 94 (8.7%) required hospitalization, and 8 (0.7%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 1,076 reports have been filed with the FAERS database.
What Other Side Effects Does DEVICE Cause?
Blood glucose increased (2,114)
Device issue (1,417)
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)
Dyspnoea (482)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which DEVICE Alternatives Have Lower Product use issue Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN