Does DEVICE Cause Expired product administered? 64 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 64 reports of Expired product administered have been filed in association with DEVICE. This represents 0.5% of all adverse event reports for DEVICE.
64
Reports of Expired product administered with DEVICE
0.5%
of all DEVICE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Expired product administered From DEVICE?
Of the 64 reports, 5 (7.8%) required hospitalization.
Is Expired product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 64 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 Expired product administered?
POLYETHYLENE GLYCOL 3350 (1,637)
NAPROXEN (1,305)
ALBUTEROL (1,233)
LORATADINE (1,095)
MINOXIDIL (982)
ACETAMINOPHEN (797)
INSULIN LISPRO (770)
FLUTICASONE\SALMETEROL (753)
CETIRIZINE (714)
DICLOFENAC (714)
Which DEVICE Alternatives Have Lower Expired product administered Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN