Does DEVICE Cause Wrong technique in product usage process? 935 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 935 reports of Wrong technique in product usage process have been filed in association with DEVICE. This represents 7.3% of all adverse event reports for DEVICE.
935
Reports of Wrong technique in product usage process with DEVICE
7.3%
of all DEVICE reports
1
Deaths
25
Hospitalizations
How Dangerous Is Wrong technique in product usage process From DEVICE?
Of the 935 reports, 1 (0.1%) resulted in death, 25 (2.7%) required hospitalization, and 4 (0.4%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 935 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)
Device leakage (795)
Injection site pain (751)
Syringe issue (634)
Product quality issue (567)
Drug ineffective (488)
Dyspnoea (482)
What Other Drugs Cause Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which DEVICE Alternatives Have Lower Wrong technique in product usage process Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN