Does DEVICE Cause Device power source issue? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Device power source issue have been filed in association with DEVICE. This represents 0.2% of all adverse event reports for DEVICE.
20
Reports of Device power source issue with DEVICE
0.2%
of all DEVICE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Device power source issue From DEVICE?
Of the 20 reports, 5 (25.0%) required hospitalization.
Is Device power source issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 20 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 Device power source issue?
SOMATROPIN (1,219)
PEGFILGRASTIM (486)
TREPROSTINIL (299)
CARBIDOPA\LEVODOPA (62)
ETANERCEPT (54)
BACLOFEN (50)
GLYCOPYRROLATE (39)
FOSCARBIDOPA\FOSLEVODOPA (14)
INTERFERON BETA-1B (13)
LECITHIN\POLOXAMER 407 (11)
Which DEVICE Alternatives Have Lower Device power source issue Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN