Does DEVICE Cause Drug administration error? 149 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 149 reports of Drug administration error have been filed in association with DEVICE. This represents 1.2% of all adverse event reports for DEVICE.
149
Reports of Drug administration error with DEVICE
1.2%
of all DEVICE reports
1
Deaths
14
Hospitalizations
How Dangerous Is Drug administration error From DEVICE?
Of the 149 reports, 1 (0.7%) resulted in death, 14 (9.4%) required hospitalization, and 2 (1.3%) were considered life-threatening.
Is Drug administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 149 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 Drug administration error?
INSULIN GLARGINE (1,189)
ACETAMINOPHEN (980)
FLUTICASONE\SALMETEROL (732)
DOCOSANOL (721)
ASPIRIN (542)
METHYLPHENIDATE (526)
NICOTINE (492)
ALBUTEROL (418)
FLUTICASONE (292)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (257)
Which DEVICE Alternatives Have Lower Drug administration error Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN