Does DEVICE Cause Incorrect dose administered by device? 95 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 95 reports of Incorrect dose administered by device have been filed in association with DEVICE. This represents 0.8% of all adverse event reports for DEVICE.
95
Reports of Incorrect dose administered by device with DEVICE
0.8%
of all DEVICE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Incorrect dose administered by device From DEVICE?
Of the 95 reports, 5 (5.3%) required hospitalization, and 2 (2.1%) were considered life-threatening.
Is Incorrect dose administered by device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 95 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 Incorrect dose administered by device?
EXENATIDE (3,332)
EVOLOCUMAB (2,840)
SOMATROPIN (2,486)
ALBUTEROL (1,236)
ETANERCEPT (1,032)
SECUKINUMAB (996)
ERENUMAB-AOOE (973)
BUDESONIDE\FORMOTEROL (753)
INSULIN GLARGINE (753)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (674)
Which DEVICE Alternatives Have Lower Incorrect dose administered by device Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN