Does DEVICE Cause Intercepted product preparation error? 1,033 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,033 reports of Intercepted product preparation error have been filed in association with DEVICE. This represents 8.1% of all adverse event reports for DEVICE.
1,033
Reports of Intercepted product preparation error with DEVICE
8.1%
of all DEVICE reports
1
Deaths
1
Hospitalizations
How Dangerous Is Intercepted product preparation error From DEVICE?
Of the 1,033 reports, 1 (0.1%) resulted in death, 1 (0.1%) required hospitalization.
Is Intercepted product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 1,033 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)
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 Intercepted product preparation error?
LEUPROLIDE (8,621)
PEGFILGRASTIM (1,514)
CARFILZOMIB (367)
BLINATUMOMAB (110)
BEVACIZUMAB-AWWB (54)
ROMIPLOSTIM (48)
TRASTUZUMAB-ANNS (42)
AFLIBERCEPT (39)
TOCILIZUMAB (26)
AVACINCAPTAD PEGOL (20)
Which DEVICE Alternatives Have Lower Intercepted product preparation error Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN