Does DEVICE Cause Device issue? 1,417 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,417 reports of Device issue have been filed in association with DEVICE. This represents 11.1% of all adverse event reports for DEVICE.
1,417
Reports of Device issue with DEVICE
11.1%
of all DEVICE reports
7
Deaths
85
Hospitalizations
How Dangerous Is Device issue From DEVICE?
Of the 1,417 reports, 7 (0.5%) resulted in death, 85 (6.0%) required hospitalization, and 6 (0.4%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 1,417 reports have been filed with the FAERS database.
What Other Side Effects Does DEVICE Cause?
Blood glucose increased (2,114)
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)
Dyspnoea (482)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which DEVICE Alternatives Have Lower Device issue Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN