Does DEVICE Cause Cataract? 122 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 122 reports of Cataract have been filed in association with DEVICE. This represents 1.0% of all adverse event reports for DEVICE.
122
Reports of Cataract with DEVICE
1.0%
of all DEVICE reports
0
Deaths
9
Hospitalizations
How Dangerous Is Cataract From DEVICE?
Of the 122 reports, 9 (7.4%) required hospitalization, and 1 (0.8%) were considered life-threatening.
Is Cataract Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 122 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 Cataract?
ADALIMUMAB (3,157)
METHOTREXATE (1,785)
INSULIN LISPRO (1,676)
LENALIDOMIDE (1,658)
ETANERCEPT (1,451)
PREDNISONE (1,365)
RITUXIMAB (1,332)
INSULIN GLARGINE (1,313)
ABATACEPT (1,065)
TOFACITINIB (1,050)
Which DEVICE Alternatives Have Lower Cataract Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN